Desafíos para enfrentar la resistencia a los antibióticos en bacterias patógenas en el tercer decenio del siglo XXI

dc.contributor.authorCabrera Alaix, Cristina Eugenia
dc.contributor.authorCerón Marín, Valentina
dc.contributor.authorChávez Vivas, Mónica
dc.contributor.authorGómez Naranjo, Rommel Fabián
dc.contributor.authorQuintero Cundumí, Sandra Lorena
dc.contributor.authorVargas Gutiérrez, Valentina
dc.contributor.cvlachttps://scienti.minciencias.gov.co/cvlac/visualizador/generarCurriculoCv.do?cod_rh=0000493724spa
dc.contributor.cvlachttps://scienti.minciencias.gov.co/cvlac/visualizador/generarCurriculoCv.do?cod_rh=0000521590spa
dc.contributor.cvlachttps://scienti.minciencias.gov.co/cvlac/visualizador/generarCurriculoCv.do?cod_rh=0000395641spa
dc.contributor.googlescholarhttps://scholar.google.com/citations?user=njSjxEIAAAAJ&hl=enspa
dc.contributor.googlescholarhttps://scholar.google.com/citations?user=8wjme4oAAAAJ&hl=esspa
dc.contributor.googlescholarhttps://scholar.google.com/citations?hl=es&user=mEyMhZAAAAAJspa
dc.contributor.orcidhttps://orcid.org/0000-0003-2884-9199spa
dc.contributor.orcidhttps://orcid.org/0000-0001-9996-3744spa
dc.contributor.orcidhttps://orcid.org/0000-0002-9529-9599spa
dc.coverage.spatialCalíspa
dc.date.accessioned2024-03-22T22:34:40Z
dc.date.available2024-03-22T22:34:40Z
dc.date.created2023
dc.description.abstractLas Infecciones bacterianas asociadas a la atención en salud constituyen en la actualidad un problema de salud pública de gran importancia que afecta a varios países del mundo. Esta problemática ha ido en aumento por la presencia de bacterias patógenas con resistencia a diversos tipos de antibióticos, debilitando los programas clínicos y de salud pública que se han diseñado para contener las enfermedades infecciosas. Este hecho se acentúa aún más en países latinoaméricanos, como es el caso de Colombia, principalmente en comunidades con un limitado acceso al servicio médico, a tratamientos oportunos y eficaces y sobre todo a la automedicación, y la disponibilidad de fármacos alterados. Inicialmente las bacterias resistentes a los antibióticos eran detectadas en infecciones relacionadas con una hospitalización reciente o cirugía, residencia prolongada en centros de cuidado, diálisis y dispositivos médicos percutáneos o catéteres. Sin embargo, a finales de los 90´s, este tipo de bacterias comenzaron a asociarse a infecciones adquiridas en la comunidad, agudizando la emergencia de enfermedades infecciosas, debido a que presentan factores de virulencia y perfiles de sensibilidad a los antibióticos propios, generando una alarma importante frente al tratamiento de estos microorganismos. El impacto negativo de la resistencia a los antibióticos ha ido en aumento porque en la última década se ha acentuado la presencia de bacterias resistentes en ambientes naturales y artificiales, favorecida en gran medida porque la mayoría de los compuestos utilizados en las prácticas médicas, veterinarias y agrícolas son vertidos de forma continua directamente en los efluentes o a las redes municipales sin metabolizar o solo parcialmente metabolizados. El grupo de investigación en enfermedades infecciosas y microbiología molecular (Gimmein) viene trabajando en la problemática que genera la resistencia bacteriana a los antibióticos desde el año 2008, inicialmente realizando investigaciones con patógenos resistentes aislados en pacientes con infecciones intrahospitalarias y en el ambiente hospitalario, y ahora en patógenos encontrados en los ambientes naturales, inclusive en insectos. Es por eso por lo que el grupo presenta el libro “Desafíos para enfrentar la resistencia a los antibióticos en bacterias patógenas en el tercer decenio del siglo XXI”, que aborda la problemática de los patógenos resistentes o multirresistentes presentes en diferentes ambientes que son potenciales fuentes de infección. En los capítulos 1 y 2 se establecen las características y mecanismos por los cuales las bacterias se hacen resistentes a los antibióticos y la epidemiología de estas en el ambiente hospitalario y en los naturales como las aguas, el suelo y en los animales a través del contacto directo por el consumo o tenencia de ellos. En los capítulos 3 y 4 se aborda la problemática de la resistencia en bacterias Gram positivas de interés clínico como son los Enterococcus sp. y los Staphylococcus sp. En el capítulo 3 se profundiza sobre el impacto que han generado las infecciones por Enterococcus faecalis, antes considerada una bacteria inocua, pero en la actualidad debido a la resistencia adquirida se le asocia con múltiples infecciones y complicaciones. En el capítulo 4 se presenta un estudio epidemiológico realizado en la ciudad de Cali con cepas de Staphylococcus aureus sensibles y resistentes a la meticilina aisladas de estudiantes de la área de la Salud. La epidemiología de bacterias Gram negativas de la familia enterobacteriácea y las no fermentadoras como Pseudomonas aeruginosa resistentes a los antibióticos, son analizadas en los capítulos siguientes. En el capítulo 5, se realiza una revisión del papel que desempeñan las bacterias resistentes del género Klebsiella y Enterobacter. Es necesario abordar la resistencia detectada en bacterias en todos estos ambientes, con el fin de sensibilizar sobre el impacto negativo que generan los patógenos resistentes en la salud pública y la necesidad de tener una efectiva vigilancia epidemiológica, que promueva el desarrollo de estrategias racionales de control en la dispersión de bacterias resistentes, lo que implica un nuevo abordaje para el tratamiento y diagnóstico de una infección.spa
dc.identifier.doihttps://doi.org/10.18041/978-958-5182-96-7
dc.identifier.isbn978-958-5182-96-7spa
dc.identifier.urihttps://hdl.handle.net/10901/28763
dc.publisherUniversidad Libre, Seccional Calispa
dc.relation.referencesAbdi, S. N., Ghotaslou, R., Ganbarov, K., Mobed, A., Tanomand, A., Yousefi, M., Asgharzadeh, M., & Kafil, H. S. (2020). Acinetobacter baumannii Efflux Pumps and Antibiotic Resistance. Infection and drug resistance, 13, 423–434.spa
dc.relation.referencesAnnavajhala, M. K., Gomez-Simmonds, A., & Uhlemann, A. C. (2019). MultidrugResistant Enterobacter cloacae Complex Emerging as a Global, Diversifying Threat. Frontiers in microbiology, 10, 44.spa
dc.relation.referencesAubry-Damon, H., Galimand, M., Gerbaud, G., Courvalin, P. (2002). rpoB mutation conferring rifampin resistance in Streptococcus pyogenes. Antimicrobial Agents and Chemotherapy, 46(5),1571–3.spa
dc.relation.referencesBush, K., Jacoby, G.A., Medeiros, A.A. (1995). A funtional classification scheme for B-lactamases and its correlation with molecular structure. Antimicrobial Agents and Chemotherapy, 39:1211-33.spa
dc.relation.referencesCattoir, V., & Leclercq, R. (2013). Twenty-five years of shared life with vancomycinresistant enterococci: Is it time to divorce. Journal of Antimicrobial Chemotherapy, 68(4), 731–42.spa
dc.relation.referencesCesur, S., Demiröz, A.P. (2013). Antibiotics and the Mechanisms of Resistance to Antibiotics. Medical Journal of Islamic World Academy of Sciences, 21(4),138–42.spa
dc.relation.referencesChang, H-H., Cohen, T., Grad, Y.H., Hanage, W.P., O’Brien, T.F., Lipsitch, M. ( 2015). Origin and Proliferation of Multiple-Drug Resistance in Bacterial Pathogens. Microbiology and Molecular Biology Reviews, 79(1),101–16.spa
dc.relation.referencesCochetti, I., Tili, E., Mingoia, M., Varaldo, P.E., Montanari, M.P. (2008). erm(B)- carrying elements in tetracycline-resistant pneumococci and correspondence between Tn1545 and Tn6003. Antimicrobial Agents and Chemotherapy, 52(4),1285–90.spa
dc.relation.referencesColca, J.R., McDonald, W.G., Waldon, D.J., Thomasco, L.M., Gadwood,R.C., Lund, E.T. (2003). Cross-linking in the living cell locates the site of action of oxazolidinone antibiotics. Journal of Biological Chemistry, 278(24), 21972–9.spa
dc.relation.referencesCornaglia, G. (2009). Fighting infections due to multidrug-resistant Grampositive pathogens. Clinical Microbiology and Infection, 15, 209–211.spa
dc.relation.referencesCornick, J.E., & Bentley, S.D. (2012). Streptococcus pneumoniae: The evolution of antimicrobial resistance to beta-lactams, fluoroquinolones and macrolides. Microbes Infection,14(7–8),573–83.spa
dc.relation.referencesCrisóstomo, M.I., Westh, H., Tomasz, A., Chung, M., Oliveira, D., de Lencastre, H. (2001). The evolution of methicillin resistance in Staphylococcus aureus: Similarity of genetic backgrounds in historically early methicillin-susceptible and -resistant isolates and contemporary epidemic clones. Proceedings of the National Academy of Sciences of the United States of America,98, 9865–9870.spa
dc.relation.referencesDaly, M.M., Doktor, S., Flamm, R., Shortridge, D. (2004). Characterization and prevalence of MefA, MefE, and the associated msr(D) gene in Streptococcus pneumoniae clinical isolates. Journal Clinic Microbiology, 42(8), 3570–4.spa
dc.relation.referencesDu, D., Wang-Kan, X., Neuberger, A., van Veen, H.W., Pos, K.M., Piddock, L. J.V., Luisi B.F. (2018). Multidrug efflux pumps: structure, function and regulation. Nature Reviews Microbiology, 16, 523–539.spa
dc.relation.referencesElkins, C.A., & Nikaido, H. (2002). Substrate specificity of the RND-type multidrug efflux pumps AcrB and AcrD of Escherichia coli is determined predominately by two large periplasmic loops. Journal of Bacteriology, 84(23), 6490–8.spa
dc.relation.referencesFalagas, M.E., Karageorgopoulos, D.E. (2008). Pandrug resistance (PDR), extensive drug resistance (XDR), and multidrug resistance (MDR) among gramnegative bacilli: Need for international harmonization in terminology. Clinical Infectious Diseases, 46(7),1121–2.spa
dc.relation.referencesFriedman, L., Alder, J.D., Silverman, J.A. (2006). Genetic changes that correlate with reduced susceptibility to daptomycin in Staphylococcus aureus. Antimicrobial Agents and Chemotherapy, (6), 2137–45.spa
dc.relation.referencesGullberg. E., Albrecht, L.M., Karlsson, C., Sandegren, L., Andersson, D.I. (2014). Selection of a multidrug resistance plasmid by sublethal levels of antibiotics and heavy metals. MBio, 5(5),19–23.spa
dc.relation.referencesHall, R.M. (2012). Integrons and gene cassettes: Hotspots of diversity in bacterial genomes. Annals of the New York Academy of Sciences,1267(1),71–8.spa
dc.relation.referencesHolt, K.E., Wertheim, H., Zadoks, R.N., Baker, S., Whitehouse, C.A., Dance, D. (2015). Genomic analysis of diversity, population structure, virulence, and antimicrobial resistance in Klebsiella pneumoniae, an urgent threat to public health. Proceedings of the National Academy of Sciences of the United States of America, 112(27, E3574–81.spa
dc.relation.referencesHooper, D. C., & Jacoby, G. A. (2015). Mechanisms of drug resistance: quinolone resistance. Annals of the New York Academy of Sciences, 1354(1), 12–31.spa
dc.relation.referencesKak, V., & Chow, J.W. (2014). Acquired Antibiotic Resistances in Enterococci. The Enterococci, 355–83.spa
dc.relation.referencesKallen, A.J., Hidron, A.I., Patel, J., Kallen, A.J., Hidron, A.I. (2014). Multidrug Resistance among Gram-Negative Pathogens That Caused HealthcareAssociated Infections Reported to the National Healthcare Safety Network , 2006 – 2008 Multidrug Resistance among Gram- Negative Pathogens That Caused Healthcare-Associated Infect, 31, 528–31spa
dc.relation.referencesKaraman, R., Jubeh, B., & Breijyeh, Z. (2020). Resistance of Gram-Positive Bacteria to Current Antibacterial Agents and Overcoming Approaches. Molecules (Basel, Switzerland), 25(12), 2888.spa
dc.relation.referencesKärpänoja, P., Nyberg, S.T., Bergman, M., Voipio, T., Paakkari, P., Huovinen, P., Sarkkinen, H., Finnish Study Group for Antimicrobial Resistance (FiRe Network). (2008). Connection between trimethoprim-sulfamethoxazole use and resistance in Streptococcus pneumoniae, Haemophilus influenzae, and Moraxella catarrhalis. Antimicrobial Agents and Chemotherapy, 52(7), 2480-5.spa
dc.relation.referencesKong, K.F., Schneper, L., Mathee, K. (2010). Beta-lactam antibiotics: From antibiosis to resistance and bacteriology. Apmis,118(1),1–36.spa
dc.relation.referencesKumar, G., Ambati, G., Tambat, R., Kumar, S., Nandanwar, H., Sobhia, M., Jachak, S. (2020). Synthesis, biological evaluation and computational studies of acrylohydrazide derivatives as potential Staphylococcus aureus NorA efflux pump inhibitors. Bioorganic Chemistry, 104, 104225spa
dc.relation.referencesMagiorakos, A.P., Srinivasan, A., Carey, R.B., Carmeli, Y., Falagas, M.E., Giske, C.G. (2012). Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: An international expert proposal for interim standard definitions for acquired resistance. Clinical Microbiology and Infection,18, 268–81.spa
dc.relation.referencesMatsuoka, M., Inoue, M., Endo, Y., Nakajima. Y. (2003). Characteristic expression of three genes, msr(A), mph(C) and erm(Y), that confer resistance to macrolide antibiotics on Staphylococcus aureus. FEMS Microbiology Letters, ;220(2), 287–93.spa
dc.relation.referencesMella, M.S., Sepúlveda, A. M., González, R.G., Bello, T.H, Domínguez, Y. M, Zemelman, Z. R. (2004). Aminoglucósidos-aminociclitoles: Características estructurales y nuevos aspectos sobre su resistencia. Revista Chilena de infectología, 21(4),330–8.spa
dc.relation.referencesMiller, S.I. (2016). Antibiotic resistance and regulation of the Gram-negative bacterial outer membrane barrier by host innate immune molecules. MBio, 7(5), 5–7.spa
dc.relation.referencesMorejón-García, M. (2013). Betalactamasas de espectro extendido. Revista Cubana de Medicina, 52(4), 272-280.spa
dc.relation.referencesNelson, R.E., Slayton, R.B., Stevens, V.W., Jones, M.M., Khader, K., Rubin, M.A. (2017). Attributable mortality of healthcare-associated infections due to multidrug-resistant gram-negative bacteria and methicillin-resistant Staphylococcus aureus. Infection Control & Hospital Epidemiology, 38(7), 848–56spa
dc.relation.referencesNikaido, H., & Pagès, J.M. (2012). Broad-specificity efflux pumps and their role in multidrug resistance of Gram-negative bacteria. FEMS Microbiology Reviews, 36(2), 340-63.spa
dc.relation.referencesPoole, K. (2001). Multidrug efflux pumps and antimicrobial resistance in Pseudomonas aeruginosa and related organisms. Journal of Molecular Microbiology and Biotechnology, 3(2), 255-64.spa
dc.relation.referencesRajagopal, M., Walker, S. (2017). Envelope Structures of Gram-Positive Bacteria. Current Topics in Microbiology and Immunology, 404, 1-44.spa
dc.relation.referencesReyes, A., Bello, H., Domínguez, M., Mella, S., Zemelman, R., González, G. (2003). Prevalence and types of class 1 integrons in aminoglycoside-resistant enterobacteriaceae from several Chilean hospitals. Journal of Antimicrobial Chemotherapy, 51(2), 317–21spa
dc.relation.referencesRichardson, L.A. (2017). Understanding and overcoming antibiotic resistance. PLOS Biology,15(8),1–5.spa
dc.relation.referencesSchindler, B.D., Kaatz, G.W. (2016). Multidrug efflux pumps of Gram-positive bacteria. Drug Resistance Updates, 27,1-1.spa
dc.relation.referencesShaw, K.J., Rather, P.N., Hare, R.S., Miller, G.H. (1993). Molecular genetics of aminoglycoside resistance genes and familial relationships of the aminoglycosidemodifying enzymes. Microbiology Review, 57(1),138–63.spa
dc.relation.referencesSoucy, S.M., Huang, J., Gogarten, J.P. (2015). Horizontal gene transfer: Building the web of life. Nature Reviews Genetics, 6(8),472–82.spa
dc.relation.referencesTafur, D., Villegas, V (2018). Mecanismos de resistencia a los antibióticos en bacterias Gram negativas. Infectio, 12(3), 217–26.spa
dc.relation.referencesValdés, M.Á.S (2017). La resistencia microbiana en el contexto actual y la importancia del conocimiento y aplicación en la política antimicrobiana. Revista Habanera de Ciencias Médicas, 6(3), 402–19spa
dc.relation.referencesVogwill, T., Kojadinovic, M., Maclean, R.C. (2016). Epistasis between antibiotic resistance mutations and genetic background shape the fitness effect of resistance across species of Pseudomonas. Proceedings of the Royal Society B: Biological Sciences, 283,1830.spa
dc.relation.referencesWichelhaus, T.A., Schäfer, V., Brade, V., Böddinghaus, B. (2001). Differential effect of rpoB mutations on antibacterial activities of rifampicin and KRM-1648 against Staphylococcus aureus. Journal of Antimicrobial Chemotherapy, 47(2), 153–6.spa
dc.relation.referencesZhong, X., Xu, H., Chen, D., Zhou, H., Hu, X., Cheng, G (2014). First emergence of acrAB and oqxAB mediated tigecycline resistance in clinical isolates of Klebsiella pneumoniae pre-dating the use of tigecycline in a Chinese Hospital. PLoS One, 9(12),1–11spa
dc.relation.referencesAgersø, Y., Jensen, L.B., Givskov, M., Roberts, M.C (2002). The identification of a tetracycline resistance gene tet(M), on a Tn916-like transposon, in the Bacillus cereus group. FEMS Microbiology Letters,214(2),251–6.spa
dc.relation.referencesAl Bayssari, C., Dabboussi, F., Hamze, M., Rolain, J.M. (2015). Emergence of carbapenemase producing Pseudomonas aeruginosa and Acinetobacter baumannii in livestock animals in Lebanon. Journal of Antimicrobial Chemotherapy,70(3),950–1.spa
dc.relation.referencesAllen, H. K., J. Donato, H. H. Wang, K. A. Cloud-Hansen, J. E. Davies, and J. Handelsman. (2010). Call of the wild: antibiotic resistance genes in natural environments. Nature Reviews Microbiology, 8, 251–259.spa
dc.relation.referencesApostolos, O.P., George, A. G, Athena, M. (2016). Antibiotic resistance profiles of Pseudomonas aeruginosa isolated from various Greek aquatic environments. FEMS Microbiology Ecology, 92(5),fiw042spa
dc.relation.referencesAquaculture system. Letters in Applied Microbiology, 51(6),611–8.spa
dc.relation.referencesAwad, A., Ramadan, H., Nasr, S., Ateya, A., Atwa, S. (2017). Genetic Characterization, Antimicrobial Resistance Patterns and Virulence Determinants of Staphylococcus aureus Isolated form Bovine Mastitis. Pakistan Journal of Biological Sciences,20(6),298-305spa
dc.relation.referencesBroszat, M., Nacke, H., Blasi, R., Siebe, C., Huebner, J., Daniel, R., & Grohmann, E. (2014). Wastewater irrigation increases the abundance of potentially harmful gammaproteobacteria in soils in Mezquital Valley, Mexico. Applied and environmental microbiology, 80(17), 5282–5291.spa
dc.relation.referencesCamiade, M., Bodilis, J., Chaftar, N., Riah-Anglet, W., Gardères, J., Buquet, S. (2020). Antibiotic resistance patterns of Pseudomonas spp. isolated from faecal wastes in the environment and contaminated surface water. FEMS Microbiology Ecology,96(2).spa
dc.relation.referencesCerqueira, F., Matamoros, V., Bayona, J., Elsinga, G., Hornstra, L.M., Piña, B. (2019). Distribution of antibiotic resistance genes in soils and crops. A field study in legume plants (Vicia faba L.) grown under different watering regimes. Environmental Research,170,16–25.spa
dc.relation.referencesCole, S.T. (2014). Who will develop new antibacterial agents?. Philosophical Transactions of the Royal Society B: Biological Sciences, 369, (1645).spa
dc.relation.referencesCostanzo, S.D., Murby, J., Bates, J. (2005). Ecosystem response to antibiotics entering the aquatic environmental. Marine Pollution Bulletin, 51, 218-223.spa
dc.relation.referencesCu,i P., Feng, L., Zhang, L., He, J., An, T., Fu, X., Li, C., Zhao, X., Zhai, Y., Li, H., Yan, W., Li, H., Luo, X., Lei, C., Wang, H., Yang, X. (2020). Antimicrobial Resistance, Virulence Genes, and Biofilm Formation Capacity Among Enterococcus species From Yaks in Aba Tibetan Autonomous Prefecture, China. Frontiers in Microbiology,12;11, 1250.spa
dc.relation.referencesCzekalski, N., Gascón Díez, E., Bürgmann, H. (2014). Wastewater as a point source of antibiotic-resistance genes in the sediment of a freshwater lake. Multidisciplinary Journal of Microbial Ecology, 8(7),1381–90.spa
dc.relation.referencesD’Costa, V.M., Griffiths, E., Wright, G.D. (2007). Expanding the soil antibiotic resistome: exploring environmental diversity. Current Opinion in Microbiology,10(5),481–9spa
dc.relation.referencesDavies, J., Davies, D. (2010). Resistance Origins and Evolution of Antibiotic. Microbiology and Molecular Biology Reviews, 74(3), 417.spa
dc.relation.referencesDíaz-Jiménez, D., García-Meniño, I., Fernández, J., García, V., Mora, A. (2020). Chicken and turkey meat: Consumer exposure to multidrugresistant Enterobacteriaceae including mcr-carriers, uropathogenic E. coli and highrisk lineages such as ST131, International Journal of Food Microbiology,331,108750.spa
dc.relation.referencesDoi, Y., Paterson, D.L., Egea, P., Pascual, A., López-Cerero, L., Navarro, M.D., Adams-Haduch, J.M., Qureshi, Z.A., Sidjabat, H.E, Rodríguez-Baño, J. (2010). Extended-spectrum and CMY-type beta-lactamase-producing Escherichia coli in clinical samples and retail meat from Pittsburgh, USA and Seville, Spain. Clinical Microbiology and Infection,16(1),33-8.spa
dc.relation.referencesDungan, R.S., Strausbaugh, C.A., Leytem,.A.B. (2019). Survey of selected antibiotic resistance genes in agricultural and non-agricultural soils in southcentral Idaho. FEMS Microbiology Ecology,;95(6),1–9spa
dc.relation.referencesEconomou V, Gousia P. (2015). Agriculture and food animals as a source of antimicrobial-resistant bacteria. Infect Drug Resist, 8, 49–61.spa
dc.relation.referencesEscolà-Vergé, L., Los-Arcos, I., Almirante, B. (2020). New antibiotics for the treatment of infections by multidrug-resistant microorganisms. Medicina Clínica,154(9),351–7.spa
dc.relation.referencesEscolà-Vergé, L., Pigrau, C., Almirante, B. (2019). Ceftolozane/tazobactam for the treatment of complicated intra-abdominal and urinary tract infections: Current perspectives and place in therapy. Infection and Drug Resistance,12,1853–67.spa
dc.relation.references. Escolà-Vergé, L., Pigrau, C., Los-Arcos, I., Arévalo, Á., Viñado, B., Campany, D., Larrosa, N., Nuvials, X., Ferrer, R., Len, O., Almirante, B. (2018). Ceftolozane/ tazobactam for the treatment of XDR Pseudomonas aeruginosa infections. Infection,46(4),461-468.spa
dc.relation.referencesEuropean Centre for Disease Prevention and Control (ECDC), European Food Safety Authority (EFSA) and European Medicines Agency (EMA). (2017). ECDC/EFSA/EMA second joint report on the integrated analysis of the consumption of antimicrobial agents and occurrence of antimicrobial resistance in bacteria from humans and food-producing animals. EFSA Journal, 15(7),4872spa
dc.relation.referencesFinley, R.L., Collignon, P., Larsson, D.G.J., Mcewen, S.A., Li, X.Z., Gaze, W.H. (2013). The scourge of antibiotic resistance: The important role of the environment. Clinical Infectious Diseases, 57(5),704-10.spa
dc.relation.referencesFrost, I., Van Boeckel, T.P., Pires, J., Craig, J., Laxminarayan, R. (2019). Global geographic trends in antimicrobial resistance: The role of international travel. Journal of Travel Medicine, 26(8),1–13.spa
dc.relation.referencesFurukawa, K., Ramesh, A., Zhou, Z., Weinberg, Z., Vallery, T., Winkler, W. C., & Breaker, R. R. (2015). Bacterial riboswitches cooperatively bind Ni(2+) or Co(2+) ions and control expression of heavy metal transporters. Molecular cell, 57(6), 1088–1098.spa
dc.relation.referencesGolob, M., Pate, M., Kušar, D., Dermota, U., Avberšek, J., Papić, B., Zdovc, I. (2019). Antimicrobial Resistance and Virulence Genes in Enterococcus faecium and Enterococcus faecalis from Humans and Retail Red Meat. BioMed research international, 9;2019,2815279.spa
dc.relation.referencesGómez, P., Lozano, C., Benito, D., Estepa, V., Tenorio, C., Zarazaga, M., Torres, C. (2016). Characterization of staphylococci in urban wastewater treatment plants in Spain, with detection of methicillin resistant Staphylococcus aureus ST398. Environmental Pollution,212,71-76.spa
dc.relation.referencesGonzaga-López, T.I., Salgado-Muñoz, T.G., Morones-Esquivel, I., MatamorosMejía, A.P., Terán-González, J.O., Arteaga-Vázquez, S., Castro-D’Franchis, L.J., Reyes-Jiménez, A.E., Mijangos-Huesca, F.J. (2016). Neumonía bacteriana, resistencia antimicrobiana e importancia de crear guías locales. Medicina Interna de México,32(3),271–6spa
dc.relation.references. Guzman-Otazo, J., Gonzales-Siles, L., Poma, V., Bengtsson-Palme, J., Thorell, K., Flach, C.F., Iñiguez, V., Sjöling, Å. (2019). Diarrheal bacterial pathogens and multi-resistant enterobacteria in the Choqueyapu River in La Paz, Bolivia. PLoS One,14;14(1),e0210735.spa
dc.relation.referencesHarada, K., Shimizu, T., Mukai, Y., Kuwajima, K., Sato, T., Kajino, A., Usui, M., Tamura, Y., Kimura, Y., Miyamoto, T., Tsuyuki, Y., Ohki, A., & Kataoka, Y. (2017). Phenotypic and molecular characterization of antimicrobial resistance in Enterobacter spp. isolates from companion animals in Japan. PloS one, 12(3), e0174178.spa
dc.relation.referencesHawkins, P., Mercado, E., Chochua, S., Castillo, M. E., Reyes, I., Chaparro, E., Gladstone, R., Bentley, S. D., Breiman, R. F., Metcalf, B. J., Beall, B., Ochoa, T. J., & McGee, L. (2017). Key features of invasive pneumococcal isolates recovered in Lima, Peru determined through whole genome sequencing. International journal of medical microbiology, 307(7), 415–421spa
dc.relation.referencesHirsch, D., Pereira, D.J., Logato, P.V.R., Piccoli, R.H., Figueiredo, H.C.P. (2006). Identificação e resistência a antimicrobianos de espécies de Aeromonas móveis isoladas de peixes e ambientes aquáticos. Ciência e Agrotecnologia, 30(6),1211–7spa
dc.relation.referencesHo, P.S. (2020). Descubrimiento de antibacterianos: desafíos del siglo XXI. Multidisciplinary Digital Publishing Institute, 9,213.spa
dc.relation.referencesHorcajada, J. P., Montero, M., Oliver, A., Sorlí, L., Luque, S., Gómez-Zorrilla, S., Benito, N., & Grau, S. (2019). Epidemiology and Treatment of MultidrugResistant and Extensively Drug-Resistant Pseudomonas aeruginosa Infections. Clinical microbiology reviews, 32(4), e00031-19..spa
dc.relation.referencesHu, Y., Cheng, H. (2014). Research Opportunities for Antimicrobial Resistance Control in China’s Factory Farming, Environmental Science and Technology, 48, 10, 5364–5.spa
dc.relation.referencesJiménez Velásquez, S.C., Torres Higuera, L.D., Parra Arango, J.L., Rodríguez Bautista, J.L., García Castro, F.E., Patiño Burbano, R.E. (2020). Profile of antimicrobial resistance in isolates of Staphylococcus spp. obtained from bovine milk in Colombia. Revista Argentina de Microbiología, 52(2),121–spa
dc.relation.referencesJohnsen, B.O., Handal, N., Meisal, R., Bjørnholt, J.V., Gaustad, P., Leegaard, T.M. (2017). erm gene distribution among Norwegian Bacteroides isolates and evaluation of phenotypic tests to detect inducible clindamycin resistance in Bacteroides species. Anaerobe, 47:226–32.spa
dc.relation.referencesJohnson, J. R., Sannes, M. R., Croy, C., Johnston, B., Clabots, C., Kuskowski, M. A., Bender, J., Smith, K. E., Winokur, P. L., & Belongia, E. A. (2007). Antimicrobial drug-resistant Escherichia coli from humans and poultry products, Minnesota and Wisconsin, 2002-2004. Emerging infectious diseases, 13(6), 838–846.spa
dc.relation.referencesKaraiskos, I., Lagou, S., Pontikis, K., Rapti, V., Poulakou, G. (2019). The “Old” and the “New” antibiotics for MDR Gram-negative pathogens: For whom, when, and how. Frontiers in Public Health, 7,1–25.spa
dc.relation.referencesKarlowsky, J.A., Hoban, D.J., Hackel, M.A., Lob, S.H., Sahm, D.F. (2017). Resistance among Gram-negative ESKAPE pathogens isolated from hospitalized patients with intra-abdominal and urinary tract infections in Latin American countries: SMART 2013–2015. The Brazilian Journal of Infectious Diseases,;21(3):343–8.spa
dc.relation.referencesKasaeva, T. Overcoming the drug-resistant TB crisis in children and adolescents. 2020;2021. (2020). Available from: https://www.who.int/news/item/20-11- 2020-overcoming-the-drug-resistanttb-crisis-in-children-and-adolescents.spa
dc.relation.referencesKhan, A., Miller, W.R., Arias, C.A. (2018). Mechanisms of antimicrobial resistance among hospital-associated pathogens. Expert Review of Antiinfective Therapy,16(4),269–87.spa
dc.relation.referencesKlotz, P., Higgins, P.G., Schaubmar, A.R., Failing, K., Leidner, U., Seifert, H., Scheufen, S., Semmler, T., Ewers, C. (2019). Seasonal Occurrence and Carbapenem Susceptibility of Bovine Acinetobacter baumannii in Germany. Frontiers in Microbiology,10,272.spa
dc.relation.referencesKnapp, C.W., Dolfing, J., Ehlert, P.A.I., Graham, D.W. (2010). Evidence of increasing antibiotic resistance gene abundances in archived soils since 1940. Environmental Science & Technology,44(2),580–7.spa
dc.relation.referencesLata, P., Ram, S., & Shanker, R. (2016). Multiplex PCR based genotypic characterization of pathogenic vancomycin resistant Enterococcus faecalis recovered from an Indian river along a city landscape. SpringerPlus, 5(1), 1199.spa
dc.relation.referencesLatorre-Barragan, M.F., Zurita-Leal, A.C., Gudiño Gomez jurado, M.E. (2019). Resistencia de los antibióticos ß-lactámicos en países latinoamericanos. Medwave,19(10),e7729.spa
dc.relation.referencesLeverstein-van H.M.A., Dierikx, C.M., Cohen, S.J, Voets, G.M., van den Munckhof, M.P., van Essen-Zandbergen, A., Platteel, T., Fluit, A.C., van de Sande-Bruinsma, N., Scharinga, J., Bonten M.J., Mevius, D.J. (2011). National ESBL surveillance group. Dutch patients, retail chicken meat and poultry share the same ESBL genes, plasmids and strains. Clin Microbiol Infect, (6),873-80.spa
dc.relation.referencesLevy-Blitchtein, S., Roca, I., Plasencia-Rebata, S., Vicente-Taboada, W., VelásquezPomar, J., Muñoz, L., Moreno-Morales, J., Pons, M. J., Del ValleMendoza, J., & Vila, J. (2018). Emergence and spread of carbapenemresistant Acinetobacter baumannii international clones II and III in Lima, Peru. Emerging microbes & infections, 7(1), 119.spa
dc.relation.referencesLi, D., Yu, T., Zhang, Y., Yang, M., Li, Z., Liu, M., & Qi, R. (2010). Antibiotic resistance characteristics of environmental bacteria from an oxytetracycline production wastewater treatment plant and the receiving river. Applied and environmental microbiology, 76(11), 3444–3451.spa
dc.relation.referencesLima, R.M.S., Figueiredo, H.C.P., Faria, F.C de, Picolli, R.H., Bueno Filho, J.S de S, Logato, P.V.R. (2006). Resistência a antimicrobianos de bactérias oriundas de ambiente de criação e filés de tilápias do nilo (Oreochromis niloticus). Ciência e Agrotecnologia.;30(1):126–32.spa
dc.relation.referencesLima, T., Domingues, S., & Da Silva, G. J. (2020). Manure as a Potential Hotspot for Antibiotic Resistance Dissemination by Horizontal Gene Transfer Events. Veterinary sciences, 7(3), 110.spa
dc.relation.referencesLloyd, D.H. (2007). Reservoirs of antimicrobial resistance in pet animals. Clinical Infectious Diseases, 45(SUPPL. 2), S148-52spa
dc.relation.referencesLopatto, E., Choi, J., Colina, A., Ma, L., Howe, A., & Hinsa-Leasure, S. (2019). Characterizing the soil microbiome and quantifying antibiotic resistance gene dynamics in agricultural soil following swine CAFO manure application. PloS one, 14(8), e0220770.spa
dc.relation.referencesLópez. L., Santamaría. J., Sánchez. A., Castro. L., Moreno. J.L. (2012). Presence of tetracycline resistant bacteria and genes in grassland-based animal production systems. Ciencia e Investigación Agraria, 39(3),411–23spa
dc.relation.referencesMalabarba, A., Goldstein, B.P. (2005). Origin, structure, and activity in vitro and in vivo of dalbavancin. Journal of Antimicrobial Chemotherapy,55(SUPPL. 2),15–20.spa
dc.relation.referencesMao, D., Luo, Y., Mathieu, J., Wang, Q., Feng, L., M, Q., Feng, C., Alvarez, P.J.J. (2014). Persistence of extracellular DNA in river sediment facilitates antibiotic resistance gene propagation. Environmental Science and Technology, 48(1),71–8.spa
dc.relation.referencesMartínez-Puchol, Sandra, Pons, María J., Ruiz-Roldán, Lidia, LaureanoAdame, Laura, Corujo, Alfredo, Ochoa, Theresa J., & Ruiz, Joaquim. (2020). Resistencia a nitrofuranos en Salmonella enterica aisladas de carne para consumo humano. Revista Peruana de Medicina Experimental y Salud Publica, 37(1), 99-103.spa
dc.relation.referencesMeng, L., Liu, H., Lan, T., Dong, L., Hu, H., Zhao, S., Zhang, Y., Zheng, N., & Wang, J. (2020). Antibiotic Resistance Patterns of Pseudomonas spp. Isolated From Raw Milk Revealed by Whole Genome Sequencing. Frontiers in microbiology, 11, 1005.spa
dc.relation.referencesMonte, D. F., Mem, A., Fernandes, M. R., Cerdeira, L., Esposito, F., Galvão, J. A., Franco, B., Lincopan, N., & Landgraf, M. (2017). Chicken Meat as a Reservoir of Colistin-Resistant Escherichia coli Strains Carrying mcr-1 Genes in South America. Antimicrobial agents and chemotherapy, 61(5), e02718-16.spa
dc.relation.referencesMuller, H., Sib, E., Gajdiss, M., Lenz-plet, F., Al, E. (2018) Dissemination of multi-resistant Gram-negative bacteria into German Wastewater and superface waters. Journal of Chemical Information and Modeling, 01(01),1689–99.spa
dc.relation.referencesNesme, J., Simonet, P. (2015).The soil resistome: A critical review on antibiotic resistance origins, ecology and dissemination potential in telluric bacteria. Environmental Microbiology, 17(4),913–30.spa
dc.relation.referencesNúñez, L., Tornello, C., Puentes, N., Moretton, J. (2012). Bacterias resistentes a antibióticos en aguas grises como agentes de riesgo sanitario. Revista Ambiente e Agua, 7(3),235–43.spa
dc.relation.referencesOrganización Mundial de la Salud (OMS). (2020). Antibiotic resistance. 31 July, 1, https://www.who.int/news-room/fact-sheets/detail/antibioticresistancespa
dc.relation.referencesOsman, K., Orabi, A., Elbehiry, A., Hanafy, M.H., Ali, A.M. (2019). Pseudomonas species isolated from camel meat: quorum sensing-dependent virulence, biofilm formation and antibiotic resistance. Future Microbiology, 14, 7, 609-622.spa
dc.relation.referencesOsman, K.M., Badr, J., Orabi, A., Elbehiry, A., Saad, A., Ibrahim, M.D.S., Hanafy, M.H. (2019). Poultry as a vector for emerging multidrug resistant Enterococcus spp.: First report of vancomycin (van) and the chloramphenicolflorfenicol (cat-fex-cfr) resistance genes from pigeon and duck faeces. Microbial Pathogenesis, 128:195-205.spa
dc.relation.referencesPappas G. (2011). An animal farm called extended-spectrum betalactamase: Antimicrobial resistance as a zoonosis. Clinical Microbiology and Infection,17(6),797–8.spa
dc.relation.referencesPayne, D.J., Gwynn, M.N., Holmes, D.J, Pompliano, D.L. (2007). Drugs for bad bugs: Confronting the challenges of antibacterial discovery. Nature Reviews Drug Discovery, 6(1),29–40.spa
dc.relation.referencesPeeters, L.E.J., Argudín, M.A., Azadikhah, S., Butaye, P. (2015). Antimicrobial resistance and population structure of Staphylococcus aureus recovered from pigs farms.Veterinary Microbiology,180(1–2),151–6.spa
dc.relation.referencesereira, A., Fariña, N., de Vega, M., González, P., Rodríguez, F., de Figueredo, L. (2016). Enterobacterias productoras de Betalactamasas de espectro extendido aisladas de pacientes ambulatorios y hospitalizados en un Laboratorio privado de Asunción. Ciencia y Salud, 1414(11),17–2417.spa
dc.relation.referencesPérez-Etayo, L., González, David., Leiva, José., Vitas, A.I. (2020). .MultidrugResistant Bacteria Isolated from Different Aquatic Environments in the North of Spain and South of France Microorganisms, 8(9), 1425.spa
dc.relation.referencesPerry, J., Waglechner, N., & Wright, G. (2016). The Prehistory of Antibiotic Resistance. Cold Spring Harbor perspectives in medicine, 6(6), a025197.spa
dc.relation.referencesPlanet. PJ., Diaz, L., Rios, R., Arias, C.A. (2016). Global spread of the communityassociated methicillin-resistant Staphylococcus aureus USA 300 Latin American Variant. Journal of Infectious Diseases, 214(10),1609–10.spa
dc.relation.referencesPorrero, C.M., Harrinson, E.M., Garayzabal, J.F., Paterson, G., Guierrier, A.D., Al, E. (2014). Detection of mecC-MRSA isolates in river water: a potential role for water in the environmental dissemination. Environmental Microbiology Reports, 6(6),705–8.spa
dc.relation.referencesPrado, T., Pereira, W.C., Silva, D.M., Seki, L.M., Carvalho, A.P.D.A., Asensi, M.D. (2008). Detection of extended-spectrum -lactamase-producing Klebsiella pneumoniae in effluents and sludge of a hospital sewage treatment plant. Letters in Applied Microbiology,46(1),136–41.spa
dc.relation.referencesQin, J., Maixnerová, M., Nemec, M., Feng, Y., Zhang, X., Nemec, A., Zong, Z. (2019). Acinetobacter cumulans sp. nov., isolated from hospital sewage and capable of acquisition of multiple antibiotic resistance genes. Systematic and Applied Microbiology, 42(3), 319–25.spa
dc.relation.referencesRahube, T.O., Marti, R., Scott, A., Tien, Y.C., Murray, Sabourin. (2014). Impact of Fertilizing with Raw or Anaerobically Digested Sewage Sludge on the Abundance of Antibiotic Resistant Coliforms, Antibiotic Resistance Genes, and Pathogenic Bacteria in Soil and on Vegetables at Harvest. Applied and Environmental Microbiology, 80(22), 6898-6907.spa
dc.relation.referencesRebouças, H., de Sousa, V., Lima, S., Vasconcelos, R., de Carvalho P.B., dos Fernandes Vieira, R.H.S. (2011). Antimicrobial resistance profile of Vibrio species isolated from marine shrimp farming environments (Litopenaeus vannamei) at Ceará, Brazil. Environmental Research,111(1),21–4spa
dc.relation.referencesRibeiro, R. V., Reis, E.M.F., Reis, C.M.F., Freitas Almeida, A.C, Rodrigues, D.P. (2010). Incidence and antimicrobial resistance of enteropathogens isolated from an integratedspa
dc.relation.referencesRibeiro, R. V., Reis, E.M.F., Reis, C.M.F., Freitas-Almeida, A.C, Rodrigues, D.P. (2010). Incidence and antimicrobial resistance of enteropathogens isolated from an integrated aquaculture system. Letters in Applied Microbiology,51(6),611–8.spa
dc.relation.referencesRodríguez, E.A., Garzón, L.M., Gómez, I.D., Jiménez, J.N. (2020). Multidrug resistance and diversity of resistance profiles in carbapenem-resistant Gramnegative bacilli throughout a wastewater treatment plant in Colombia. Journal of Global Antimicrobial Resistance,22,358–66.spa
dc.relation.referencesRomeu Álvarez, B., Salazar Jiménez, P., Lugo Moya, D., Rojas Hernández, N.M,. Eslava Campos, C.A. (2012). Susceptibilidad antimicrobiana de aislamientos de Escherichia coli procedentes de ecosistemas dulceacuícolas. Revista Cubana de Medicina Tropical, 64(2), 132-141.spa
dc.relation.referencesSanmartín, B., Bravo, V., Borie, C. (2005). Evaluacion de la resistencia antimicrobiana en ganado bovino en Chile, utilizando E.coli como bacteria indicadora. Archivos de Medicina Veterinaria, 37(2),117–23spa
dc.relation.referencesSánchez, M.P., Gutiérrez, N.P., Padilla, M.Y., Suárez, L.L. (2015). Resistencia antimicrobiana de bacterias aisladas de clínicas veterinarias de la ciudad de Ibagué, Colombia. Revista Universidad y Salud, 17(1),18-31.spa
dc.relation.referencesSánchez-Baena, A. M., Caicedo-Bejarano, L. D., & Chávez-Vivas, M. (2021). Structure of Bacterial Community with Resistance to Antibiotics in Aquatic Environments. A Systematic Review. International journal of environmental research and public health, 18(5), 2348.spa
dc.relation.referencesSantestevan, N.A., de Angelis Zvoboda, D., Prichula, J., Pereira, R.I., Wachholz, G.R., Cardoso, L.A., de Moura, T.M., Medeiros, A.W., de Amorin, D.B., Tavares, M., d’Azevedo, P.A., Franco, A.C., Frazzon, J., Frazzon, A.P. (2015). Antimicrobial resistance and virulence factor gene profiles of Enterococcus spp. isolates from wild Arctocephalus australis (South American fur seal) and Arctocephalus tropicalis (Subantarctic fur seal). World Journal of Microbiology & Biotechnology, 31(12),1935-46.spa
dc.relation.referencesSavin, M., Bierbaum, G, Hammerl, A., Heinemann, C., Parcina, M., Sib, E. (2020). ESKAPE Bacteria and Exten.ded-Spectrum--Lactamase Producing Escherichia coli Isolated from Wastewater and Process Water from German Poultry Slaughterhouses. Applied and Environmental Microbiology Journal, 86(8):1–18spa
dc.relation.referencesShirley, M. (2018). Ceftazidime-Avibactam: A Review in the Treatment of Serious Gram-Negative Bacterial Infections. Drugs, 78(6),675–92.spa
dc.relation.referencesSilva E Souza, D.G., Avelar, K.E.S., Antunes, L.C.M., Lobo, L.A., Domingues, R.M.C.P., De Souza Ferreira, M.C. (2000). Resistance profile of Bacteroides fragilis isolated in Brazil. Do they shelter the cfiA gene? Journal of Antimicrobial Chemotherapy, 45(4),475–81spa
dc.relation.referencesSilver, L.L. (2011). Challenges of antibacterial discovery. Clinical Microbiology Reviews Journal, 24(1),71–109.spa
dc.relation.references. Storteboom, H., Arabi, M. (2010). Identification of antibiotic-resistance-gene Molecular signatures suitable as tracers of pristine river, urban and agricultural sources. Environmental Science and Technology, 44(6),1947–53.spa
dc.relation.referencesTamborini, A.L., Casabona, L.M., Viñas, M.R., Asato, V., Hoffer, A., Farace, M.I., Lucero, M.C., Corso, A., Pichel, M. (2012). Campylobacter spp.: prevalencia y caracterización feno-genotípica de aislamientos de pacientes con diarrea y de sus mascotas en la provincia de La Pampa, Argentina [Campylobacter spp.: prevalence and pheno-genotypic characterization of isolates recovered from patients suffering from diarrhea and their pets in La Pampa Province, Argentina]. Revista Argentina de Microbiología, 44(4),266-spa
dc.relation.referencesTavakol, M., Momtaz, H., Mohajeri, P., Shokoohizadeh, L., & Tajbakhsh, E. (2018). Genotyping and distribution of putative virulence factors and antibiotic resistance genes of Acinetobacter baumannii strains isolated from raw meat. Antimicrobial resistance and infection control, 7, 120.spa
dc.relation.referencesTiseo, K., Huber, L., Gilbert, M., Robinson, T. P., & Van Boeckel, T. P. (2020). Global Trends in Antimicrobial Use in Food Animals from 2017 to 2030. Antibiotics (Basel, Switzerland), 9(12), 918.spa
dc.relation.referencesTobudic, S., Forstner, C., Burgmann, H., Lagler, H., Ramharter, M., Steininger, C., Vossen, M., Winkler, S., Thalhammer, F. (2018). Dalbavancin as primary and sequential treatment for gram-positive infective endocarditis: 2-year experience at the general hospital of Vienna. Clinical Infectious Diseases,67(5),795–798.spa
dc.relation.referencesTommasi, R., Iyer, R., Miller, A.A. (2018). Antibacterial Drug Discovery: Some Assembly Required. ACS Infectious Diseases,4(5),686–95.spa
dc.relation.referencesUgarte Silva, R.G, Olivo López., J.M., Corso, A., Pasteran, F., Albornoz, E., & Sahuanay Blácido, Z.P. (2018). Resistencia a colistín mediado por el gen mcr-1 identificado en cepas de Escherichia coli y Klebsiella pneumoniae: primeros reportes en el Perú. Anales de la Facultad de Medicina, 79(3), 213217.spa
dc.relation.referencesVivas, M.C., Caicedo, L.D., Castillo, J.E. (2019). Occurrence of LactamaseProducing Gram-Negative Bacterial Isolates in Water Sources in Cali City, Colombia. International Journal Microbiology,2019spa
dc.relation.referencesWarren, R. E., Ensor, V. M., O’Neill, P., Butler, V., Taylor, J., Nye, K., Harvey, M., Livermore, D. M., Woodford, N., Hawkey, P. M. (2008). Imported chicken meat as a potential source of quinolone-resistant Escherichia coli producing extended-spectrum -lactamases in the UK, Journal of Antimicrobial Chemotherapy, 61, 3, 504–508.spa
dc.relation.referencesWatkins, R. R., Holubar, M., & David, M. Z. (2019). Antimicrobial resistance in methicillin-resistant Staphylococcus aureus to newer antimicrobial agents. Antimicrobial agents and chemotherapy, 63(12), e01216-19.spa
dc.relation.referencesWellington, E.M.H., Boxall, A.B.A., Cross, P., Feil, E.J., Gaze, W.H., Hawkey, P.M. (2013). The role of the natural environment in the emergence of antibiotic resistance in Gram-negative bacteria. Lancet infectious diseases,13(2),155–65.spa
dc.relation.referencesWu, N., Zhang, W., Xie, S., Zeng, M., Liu, H., Yang, J., Liu, X., Yang, F. (2020). Increasing prevalence of antibiotic resistance genes in manured agricultural soils in northern China. Frontiers of Environmental Science & Engineering,14(1),1–12.spa
dc.relation.referencesXi, C., Zhang, Y., Marrs, C. F., Ye, W., Simon, C., Foxman, B., & Nriagu, J. (2009). Prevalence of antibiotic resistance in drinking water treatment and distribution systems. Applied and environmental microbiology, 75(17), 5714-5718.spa
dc.relation.referencesXiong, W., Sun, Y., Zhang, T., Ding, X., Li, Y., Wang, M. (2015). Antibiotics, Antibiotic Resistance Genes, and Bacterial Community Composition in Fresh Water Aquaculture Environment in China. Microbial Ecology, 70(2),425–32.spa
dc.relation.referencesXu, T., Zhang, C., Ji, Y., Song, J., Liu, Y., Guo, Y., Zhou, K. (2021). Identification of mcr-10 carried by self-transmissible plasmids and chromosome in Enterobacter roggenkampii strains isolated from hospital sewage water. Environmental Pollution, 268(Pt B),115706.spa
dc.relation.referencesYadav, R., Kumar, A., Singh, V.K., Jayshree., Yadav, S.K. (2018). Prevalence and antibiotyping of Staphylococcus aureus and methicillinresistant S. aureus (MRSA) in domestic animals in India. Journal of Global Antimicrobial Resistance,15,222–5.spa
dc.relation.references.Zhang, R., Liu, Z., Li, J., Lei, L., Yin, W., Li, M., Wu, C., Walsh, T. R., Wang, Y., Wang, S., & Wu, Y. (2017). Presence of VIM-Positive Pseudomonas Species in Chickens and Their Surrounding Environment. Antimicrobial agents and chemotherapy, 61(7), e00167-17.spa
dc.relation.referencesZhu, Y. G., Zhao, Y., Zhu, D., Gillings, M., Penuelas, J., Ok, Y. S., Capon, A., & Banwart, S. (2019). Soil biota, antimicrobial resistance and planetary health. Environment International, 131, [105059].spa
dc.relation.referencesAbranches, J., Tijerina, P., Avilés-Reyes, A., Gaca, A.O., Kajfasz, J.K., Lemos, J.A. (2013). The Cell Wall-Targeting Antibiotic Stimulon of Enterococcus faecalis. PLoS One,8(6), e64875. http://journals.plos.org/plosone/article/ asset?id=10.1371%2Fjournal.pone.0 064875.PDF68.spa
dc.relation.referencesAgaba, P., Tumukunde, J., Tindimwebwa, J., & Kwizera, A. (2017). Nosocomial bacterial infections and their antimicrobial susceptibility patterns among patients in Ugandan intensive care units: a cross sectional study. BMC research notes, 10(1), 349. https://doi.org/10.1186/s13104-017-26955spa
dc.relation.referencesAgudelo Higuita, N.I., Huycke, M.M. (2014). Enterococcal Disease, Epidemiology, and Implications for Treatment. In: Gilmore MS, Clewell DB, Ike Y, et al., editors. Enterococci: From Commensals to Leading Causes of Drug Resistant Infection. Boston: Massachusetts Eye and Ear Infirmary; 2014-. https://www.ncbi.nlm.nih. gov/books/NBK190429/spa
dc.relation.referencesAgudelo Higuita, N.I., Huycke, M.M. Enterococcal Disease, Epidemiology, and Implications for Treatment. (2014). In: Gilmore MS, Clewell DB, Ike Y, et al., editors. Enterococci: From Commensals to Leading Causes of Drug Resistant Infection [Internet]. Boston: Massachusetts Eye and Ear Infirmary; 2014-. Available from: https://www.ncbi.nlm.nih.gov/books/NBK190429/spa
dc.relation.referencesAhmadpoor, N., Ahmadrajabi, R., Esfahani, S., Hojabri, Z., Moshafi, M.H., Saffari, F (2021). High-Level Resistance to Erythromycin and Tetracycline and Dissemination of Resistance Determinants among Clinical Enterococci in Iran. Medical Principles and Practice, 30,272-276.spa
dc.relation.referencesArancibia, F & Montufar, F. (2011). Prevalence of nosocomial infection in Latin American intensive care units. International Journal of Infection Control, 7, 1-5. 10.3396/ijic.V7i4.039.11.spa
dc.relation.referencesArbeloa, A., Segal, H., Hugonnet, J. E., Josseaume, N., Dubost, L., Brouard, J. P., Gutmann, L., Mengin-Lecreulx, D., & Arthur, M. (2004). Role of class A penicillin-binding proteins in PBP5-mediated beta-lactam resistance in Enterococcus faecalis. Journal of bacteriology, 186(5), 1221–1228. https://doi. org/10.1128/JB.186.5.1221-1228.2004spa
dc.relation.referencesArias, C. A., Panesso, D., McGrath, D. M., Qin, X., Mojica, M. F., Miller, C., Diaz, L., Tran, T. T., Rincon, S., Barbu, E. M., Reyes, J., Roh, J. H., Lobos, E., Sodergren, E., Pasqualini, R., Arap, W., Quinn, J. P., Shamoo, Y., Murray, B. E., & Weinstock, G. M. (2011). Genetic basis for in vivo daptomycin resistance in enterococci. The New England journal of medicine, 365(10), 892–900. https://doi.org/10.1056/ NEJMoa1011138spa
dc.relation.referencesArias, C.A., Murray, B.E. (2012). The rise of the Enterococcus: beyond vancomycin resistance. Nature Reviews Microbiology,10(4),266-78.spa
dc.relation.referencesAyeni, F. A., Odumosu, B. T., Oluseyi, A. E., & Ruppitsch, W. (2016). Identification and prevalence of tetracycline resistance in enterococci isolated from poultry in Ilishan, Ogun State, Nigeria. Journal of pharmacy & bioallied sciences, 8(1), 69–73. https://doi.org/10.4103/0975-7406.171729spa
dc.relation.referencesAyobami, O., Willrich, N., Reuss, A., Eckmanns, T., & Markwart, R. (2020). The ongoing challenge of vancomycin-resistant Enterococcus faecium and Enterococcus faecalis in Europe: an epidemiological analysis of bloodstream infections. Emerging microbes & infections, 9(1), 1180–1193. https://doi.org/10.1080/222217 51.2020.1769500spa
dc.relation.referencesAzzouz A, Preuss CV. Linezolid. (2021). In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2021 Jan-. Available from: https://www.ncbi.nlm.nih. gov/books/NBK539793/spa
dc.relation.referencesBarnes, A., Dale, J. L., Chen, Y., Manias, D. A., Greenwood Quaintance, K. E., Karau, M. K., Kashyap, P. C., Patel, R., Wells, C. L., & Dunny, G. M. (2017). Enterococcus faecalis readily colonizes the entire gastrointestinal tract and forms biofilms in a germ-free mouse model. Virulence, 8(3), 282–296. https://doi.org /10.1080/21505594.2016.1208890spa
dc.relation.referencesBeganovic, M., Luther, M. K., Kristich , L. B., Arias, C. A., Rybak, M. J., & LaPlante, K. L. (2018). A Review of Combination Antimicrobial Therapy for Enterococcus faecalis Bloodstream Infections and Infective Endocarditis. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 67(2), 303–309. https://doi.org/10.1093/cid/ciy064spa
dc.relation.referencesBehnood, A., Farajnia, S., Moaddab, S. R., Ahdi-Khosroshahi, S., & Katayounzadeh, A. (2013). Prevalence of aac(6’)-Ie-aph(2 )-Ia resistance gene and its linkage to Tn5281 in Enterococcus faecalis and Enterococcus faecium isolates from Tabriz hospitals. Iranian journal of microbiology, 5(3), 203–208.spa
dc.relation.referencesBender, E. A., de Freitas, A. L., Reiter, K. C., Lutz, L., & Barth, A. L. (2009). Identification, antimicrobial resistance and genotypic characterization of Enterococcus spp. isolated in Porto Alegre, Brazil. Brazilian journal of microbiology, 40(3), 693–700. https://doi.org/10.1590/S1517-838220090003000035spa
dc.relation.referencesBourafa, N., Abat, C., Loucif, L., Olaitan, A.O., Bentorki, A.A., Boutefnouchet, N., Rolain, J.M. (2016). Identification of vancomycin-susceptible major clones of clinical Enterococcus from Algeria. Journal of Global Antimicrobial Resistance,6:78-83.spa
dc.relation.referencesBrown, S. P., Cornforth, D. M., & Mideo, N. (2012). Evolution of virulence in opportunistic pathogens: generalism, plasticity, and control. Trends in microbiology, 20(7), 336–342. https://doi.org/10.1016/j.tim.2012.04.005.spa
dc.relation.referencesCabrera, C.E., Gómez, R.F, Zúñiga, A.E., Corral, R.H., López, B., & Chávez, M. (2011). Epidemiology of nosocomial bacteria resistant to antimicrobials. Colombia Médica, 42(1), 117-125. Recuperado en 10 de noviembre de 2021, de http://www.scielo.org.co/scielo.phspa
dc.relation.referencesCai., J, Wang, Y., Schwarz, S., Lv, H., Li, Y., Liao, K., Yu, S., Zhao, K., Gu, D., Wang, X., Zhang, R., Shen, J. (2015). Enterococcal isolates carrying the novel oxazolidinone resistance gene optrA from hospitals in Zhejiang, Guangdong, and Henan, China, 2010-2014. Clinical Microbiology and Infection,21(12),1095.e1-4.spa
dc.relation.referencesCasellas JM. Resistencia a los antibacterianos en América Latina: consecuencias para la infectología. Rev Panam Salud Pública. 2011; 30(6):519–28.spa
dc.relation.referencesCattoir, V., Leclercq, R. (2013). Twenty-five years of shared life with vancomycinresistant Enterococci: is it time to divorce? J Antimicrob Chemother,68,731–42.spa
dc.relation.referencesCavaco, L.M., Bernal, J.F., Zankari, E., Léon, M., Hendriksen, R.S., PerezGutierrez, E., Aarestrup, F.M., Donado-Godoy, P. (2017). Detection of linezolid resistance due to the optrA gene in Enterococcus faecalis from poultry meat from the American continent (Colombia). Journal of Antimicrobial Chemotherapy,72(3),678-683.spa
dc.relation.referencesCeci, M., Delpech, G., Sparo, M., Mezzina, V., Sánchez Bruni, S., & Baldaccini, B. (2015). Clinical and microbiological features of bacteremia caused by Enterococcus faecalis. Journal of infection in developing countries, 9(11), 1195–1203. https://doi. org/10.3855/jidc.6587spa
dc.relation.referencesCenters for Disease Control and Prevention. Antibiotic resistance threats in the United States (2013). www.cdc.gov/drugresistance/pdf/ar-threats-2013508spa
dc.relation.referencesChen, H., Wu, W., Ni, M., Liu, Y., Zhang, J., Xia, F., He, W., Wang, Q., Wang, Z., Cao, B., Wang, H. (2013). Linezolid-resistant clinical isolates of enterococci and Staphylococcus cohnii from a multicentre study in China: molecular epidemiology and resistance mechanisms. International Journal of Antimicrobial Agents, 42(4),317-21.spa
dc.relation.referencesClinical and Laboratory Standard Institute (CLSI). (2018). .Performance Standards for Antimicrobial Susceptibility Testing; 28th ed. CLSI supplement M100. Wayne: Clinical and Laboratory Standards Institute.spa
dc.relation.referencesCohen, A. L., Roh, J. H., Nallapareddy, S. R., Höök, M., & Murray, B. E. (2013). Expression of the collagen adhesin ace by Enterococcus faecalis strain OG1RF is not repressed by Ers but requires the Ers box. FEMS microbiology letters, 344(1), 18–24. https://doi.org/10.1111/15746968.12146spa
dc.relation.referencesConceição, N., Rodrigues, W.F., de Oliveira, K.L.P., Pinheiro L.E., Rezende L., de Cunha Hueb Barata, C., Gonçalves, A. (2020). Beta-lactams susceptibility testing of penicillin-resistant, ampicillin-susceptible Enterococcus faecalis isolates: a comparative assessment of Etest and disk diffusion methods against broth dilution. Annals of Clinical Microbiology and Antimicrobials,19, 43 https:// doi.org/10.1186/s12941-020-00386-8.spa
dc.relation.referencesConde-Estévez, D., Sorli, L., Morales-Molina, J. A., Knobel, H., Terradas, R., Mateu-de Antonio, J., Horcajada, J. P., & Grau, S. (2010). Características clínicas diferenciales entre las bacteriemias por Enterococcus faecalis y Enterococcus faecium. Enfermedades infecciosas y microbiologia clinica, 28(6), 342–348. https:// doi.org/10.1016/j.eimc.2009.06.011spa
dc.relation.referencesCorrea, L., Gaona, C.E., Pierna, M., de la Fuente, R., González, C., Sacristán, B. (2018). Meningitis neonatal por Enterococcus faecalis. Revista del Laboratorio Clínico,11(2), 101-103.spa
dc.relation.referencesDahl A., Bruun N.E. Enterococcus faecalis infective endocarditis: Focus on clinical aspects. Expert Rev. Cardiovasc. Ther. 2013;11:1247–1257.spa
dc.relation.referencesDavlieva, M., Zhang, W., Arias, C. A., & Shamoo, Y. (2013). Biochemical characterization of cardiolipin synthase mutations associated with daptomycin resistance in enterococci. Antimicrobial agents and chemotherapy, 57(1), 289–296. https://doi.org/10.1128/AAC.01743-12.spa
dc.relation.references. de Almeida, L. M., de Araújo, M. R., Iwasaki, M. F., Sacramento, A. G., Rocha, D., da Silva, L. P., Pavez, M., de Brito, A. C., Ito, L. C., Gales, A. C., Lincopan, N., Sampaio, J. L., & Mamizuka, E. M. (2014). Linezolid resistance in vancomycinresistant Enterococcus faecalis and Enterococcus faecium isolates in a Brazilian hospital. Antimicrobial agents and chemotherapy, 58(5), 2993–2994. https://doi. org/10.1128/AAC.02399-14.spa
dc.relation.references. de Regt, M. J., van Schaik, W., van Luit-Asbroek, M., Dekker, H. A., van Duijkeren, E., Koning, C. J., Bonten, M. J., & Willems, R. J. (2012). Hospital and community ampicillin-resistant Enterococcus faecium are evolutionarily closely linked but have diversified through niche adaptation. PloS one, 7(2), e30319. https://doi. org/10.1371/journal.pone.0030319.spa
dc.relation.referencesDeterminant of Intestinal Colonization, Journal of Infectious Diseases, 211(1), 62–71, https://doi.org/10.1093/infdis/jiu402.spa
dc.relation.referencesDiab, M., Salem, D., El-Shenawy, A Amira El-Far, Aya Abdelghany, Alaa Reda Awad, Inas El Defrawy & Mohamed Shemis. (2019). Detection of high level aminoglycoside resistance genes among clinical isolates of Enterococcus species. Egyptian Journal of Medical Human Genetics, 20,28), https://doi.org/10.1186/ s43042-019-0032-3.spa
dc.relation.referencesDíaz, L., Kiratisin, P., Mendes, R. E., Panesso, D., Singh, K. V., & Arias, C. A. (2012). Transferable plasmid-mediated resistance to linezolid due to cfr in a human clinical isolate of Enterococcus faecalis. Antimicrobial agents and chemotherapy, 56(7), 3917–3922. https://doi.org/10.1128/AAC.00419-12.spa
dc.relation.referencesDönhöfer, A., Franckenberg, S., Wickles, S., Berninghausen, O., Beckmann, R., Wilson D.N. (2012). Structural basis for TetM-mediated tetracycline resistance. Proceedings of the National Academy of Sciences,109(42),16900-16905; https://doi. org/10.1073/pnas.1208037109.spa
dc.relation.referencesECDC. (2019). Surveillance of antimicrobial resistance in Europe 2018. Stockholm: European Centre for Disease Prevention and Control.spa
dc.relation.referencesEdelsberg, J., Weycker, D., Barron, R., Li, X., Wu, H., Oster, G., Badre, S., Langeberg, W.J., Weber, D.J. (2014). Prevalence of antibiotic resistance in US hospitals. Diagnostic Microbiology and Infectious Disease, 78,255–62.spa
dc.relation.referencesEngland, P.H. (2014). Identifcation of Streptococcus species, Enterococcus species and morphologically similar organisms. UK Standards for microbiology investigations,4,1–36.spa
dc.relation.referencesEPINE-EPPS (2015). Estudio de Prevalencia de las Infecciones Nosocomiales en España. Sociedad Española de Medicina Preventiva, Salud Pública e Higiene. http://hws.vhebron.net/epine/.spa
dc.relation.referencesEuropean Centre for Disease Prevention and Control. (2015). Antimicrobial resistance surveillance in Europe 2014. Annual Report of the European Antimicrobial Resistance Surveillance Network (EARS-Net). Stockholm: ECDC;. http://www.ecdc.europa.eu.spa
dc.relation.referencesFernández-Hidalgo, N., Escolà-Vergé, L., & Pericàs, J. M. (2020). Enterococcus faecalis endocarditis: what’s next?. Future microbiology, 15, 349–364. https://doi. org/10.2217/fmb-2019-0247.spa
dc.relation.referencesFiore, E., Van Tyne, D., & Gilmore, M. S. (2019). Pathogenicity of Enterococci. Microbiology spectrum, 7(4), 10.1128/microbiolspec.GPP3-0053-2018. https://doi. org/10.1128/microbiolspec.GPP3-0053-2018.spa
dc.relation.referencesFlores-Mireles, A. L., Walker, J. N., Caparon, M., & Hultgren, S. J. (2015). Urinary tract infections: epidemiology, mechanisms of infection and treatment options. Nature reviews. Microbiology, 13(5), 269–284. https://doi.org/10.1038/ nrmicro3432.spa
dc.relation.referencesGagetti, P., Bonofiglio, L., Gabarrot, G., Kaufman, S., Mollerach, M., Vigliarolo, L., von Specht, M., Toresani, I., Lopardo, H.A. (2019). Resistance to -lactams in enterococci. Revista Argentina de Microbiología, 51(2),179183.spa
dc.relation.referencesGalimand, M., Schmitt, E., Panvert, M., Desmolaize, B., Douthwaite, S., Mechulam, Y., & Courvalin, P. (2011). Intrinsic resistance to aminoglycosides in Enterococcus faecium is conferred by the 16S rRNA m5C1404-specific methyltransferase EfmM. RNA (New York, N.Y.), 17(2), 251–262. https://doi.org/10.1261/rna.2233511.spa
dc.relation.referencesGandra, S., Braykov, N., Laxminarayan, R. (2013). East North Central Region Has the Highest Prevalence of Vancomycin-Resistant Enterococcus faecalis in the United States. Infection Control and Hospital Epidemiology, 34(4),443-5.spa
dc.relation.referencesGarcía-Solache, M., & Rice, L. B. (2019). The Enterococcus: a Model of Adaptability to Its Environment. Clinical microbiology reviews, 32(2), e0005818. Https:// doi.org/10.1128/CMR.00058-18spa
dc.relation.referencesGilmore, M. S., Rauch, M., Ramsey, M. M., Himes, P. R., Varahan, S., Manson, J. M., Lebreton, F., & Hancock, L. E. (2015). Pheromone killing of multidrug-resistant Enterococcus faecalis V583 by native commensal strains. Proceedings of the National Academy of Sciences of the United States of America, 112(23), 7273–7278. https:// doi.org/10.1073/pnas.1500553112.spa
dc.relation.referencesGoh, H., Yong, M., Chong, K., & Kline, K. A. (2017). Model systems for the study of Enterococcal colonization and infection. Virulence, 8(8), 1525–1562. https://doi.org/10.1080/21505594.2017.1279766.spa
dc.relation.referencesGuffey, A.A., Loll P.J. (2021). Regulation of Resistance in VancomycinResistant Enterococci: The VanRS Two-Component System. Microorganisms, 9(10), 2026. https://doi.org/10.3390/microorganisms9102026.spa
dc.relation.referencesGupta K, Bhadelia N. (2014). Management of urinary tract infections from multidrug-resistant organisms. Infectious Disease Clinics of North America, 28(1),49–59.spa
dc.relation.referencesGuzman Prieto, A. M., van Schaik, W., Rogers, M. R., Coque, T. M., Baquero, F., Corander, J., & Willems, R. J. (2016). Global Emergence and Dissemination of Enterococci as Nosocomial Pathogens: Attack of theClones?. Frontiers in microbiology, 7, 88. https://doi.org/10.3389/fmicb.2016.00788.spa
dc.relation.referencesHall, C.L., Tschannen, M., Worthey, E.A., Kristich, C.J. (2013). IreB, a Ser/Thr kinase substrate, influences antimicrobial resistance in Enterococcus faecalis. Antimicrobial Agents and Chemotherapy, 57(12),6179-86. doi: 10.1128/AAC.01472-13.spa
dc.relation.referencesHe, T., Shen, Y., Schwarz, S., Cai, J., Lv, Y., Li, J., Feßler, A.T., Zhang, R., Wu, C., Shen, J., Wang, Y. (2016). Genetic environment of the transferable oxazolidinone/ phenicol resistance gene optrA in Enterococcus faecalis isolates of human and animal origin. Journal of Antimicrobial Chemotherapy,71(6),1466-73.spa
dc.relation.referencesHegstad, K., Mikalsen, T., Coque, T.M., Werner, G., Sundsfjord, A. (2010). Mobile genetic elements and their contribution to the emergence of antimicrobial resistant Enterococcus faecalis and Enterococcus faecium. Clinical Microbiology and Infection,16 (6), 541-54.spa
dc.relation.referencesHollenbeck, B.L., Rice, L.B. (2012). Intrinsic and acquired resistance mechanisms in Enterococcus. Virulence,3(5),421-33.spa
dc.relation.referencesHumphries, R. M., Pollett, S., & Sakoulas, G. (2013). A current perspective on daptomycin for the clinical microbiologist. Clinicalspa
dc.relation.referencesInstituto de Salud Pública de Chile. (2013). Vigilancia de Enterococcus spp. resistente a Vancomicina Chile, 2010-2012. Boletín Instituto de Salud Pública de Chile 3,10.spa
dc.relation.referencesInstituto Nacional de Salud. Vigilancia de Resistencia bacteriana (Whonet) Primer semestre año 2015. Dirección de Redes en Salud Pública. Despacho Dirección de Redes. Bogotá, Diciembre de 2015.spa
dc.relation.referencesIsenman, H., Michaels, J. & Fisher, D. (2016). Global variances in infection control practices for vancomycin resistant Enterococcus – results of an electronic survey. Antimicrobial Resistance and Infection Control, 5, 41 https://doi.org/10.1186/ s13756-016-0140-5.spa
dc.relation.referencesJabbari Shiadeh, S. M., Pormohammad, A., Hashemi, A., & Lak, P. (2019). Global prevalence of antibiotic resistance in blood-isolated Enterococcus faecalis and Enterococcus faecium: a systematic review and meta-analysis. Infection and drug resistance, 12, 2713–2725. https://doi.org/10.2147/IDR.S206084.spa
dc.relation.referencesJabbari Shiadeh, S. M., Pormohammad, A., Hashemi, A., & Lak, P. (2019). Global prevalence of antibiotic resistance in blood-isolated Enterococcus faecalis and Enterococcus faecium: a systematic review and meta-analysis. Infection and drug resistance, 12, 2713–2725. https://doi.org/10.2147/IDR.S206084.spa
dc.relation.referencesKang, S.W., Lee, S.J., Choi, S.S. (2015). Distribution of Multidrug Efflux Pump Genes in Enterococci spp. Isolated from Bovine Milk Samples and Their Antibiotic Resistance Patterns. Korean Journal of Microbiology,49(2),126-130.spa
dc.relation.referencesKellogg, S.L., Kristich, C.J. (2016). Functional Dissection of the CroRS TwoComponent System Required for Resistance to Cell Wall Stressors in Enterococcus faecalis. Journal of Bacteriology, 31;198(8):1326-36. doi: 10.1128/ JB.00995-15.spa
dc.relation.referencesKhodabandeh, M., Mohammadi, M., Abdolsalehi, M.R., Hasannejad-Bibalan, M., Gholami, M., Alvandimanesh, A., Pournajaf, A., Rajabnia, R. (2020). High-Level Aminoglycoside Resistance in Enterococcus Faecalis and Enterococcus Faecium; as a Serious Threat in Hospitals. Infectious Disorders - Drug Targets, 20(2),223-228.spa
dc.relation.referencesKristich CJ, Rice LB, Arias CA. (2014). Enterococcal Infection—Treatment and Antibiotic Resistance. Enterococci From Commensals to Lead Causes. Infection and Drug Resistance,87–134.spa
dc.relation.referencesKristich, C.J., Little, J.L., Hall, C.L., Hoff, J.S. (2011). Reciprocal regulation of cephalosporin resistance in Enterococcus faecalis. mBio, 2,e00199-11. doi:10.1128/mBio.00199-11.spa
dc.relation.referencesLa Rosa, S. L., Montealegre, M. C., Singh, K. V., & Murray, B. E. (2016). Enterococcus faecalis Ebp pili are important for cell-cell aggregation and intraspecies gene transfer. Microbiology (Reading, England), 162(5), 798–802. https://doi. org/10.1099/mic.0.000276.spa
dc.relation.referencesLaverde Gómez, J. A., Hendrickx, A. P., Willems, R. J., Top, J., Sava, I., Huebner, J., Witte, W., & Werner, G. (2011). Intra- and interspecies genomic transfer of the Enterococcus faecalis pathogenicity island. PloS one, 6(4), e16720. https://doi. org/10.1371/journal.pone.0016720.spa
dc.relation.referencesLavilla, L., Benomar, N., Sánchez, A., Casado, M.C., Gálvez, A., Abriouel, H. (2014). Role of EfrAB efflux pump in biocide tolerance and antibiotic resistance of Enterococcus faecalis and Enterococcus faecium isolated from traditional fermented foods and the effect of EDTA as EfrAB inhibitor. Food Microbiology, 44,249-257.spa
dc.relation.referencesLebeaux, D., Fernández-Hidalgo, N., Pilmis, B., Tattevin, P., Mainardi, J.L. (2020). Aminoglycosides for infective endocarditis: time to say goodbye?. Clinical Microbiology and Infection 26(6),723-728. https://doi.org/10.1016/j. cmi.2019.10.017.spa
dc.relation.referencesLebreton, F., Depardieu, F., Bourdon, N., Fines-Guyon, M., Berger, P., Camiade, S., Leclercq, R., Courvalin, P., & Cattoir, V. (2011). D-Ala-d-Ser VanN-type transferable vancomycin resistance in Enterococcus faecium. Antimicrobial agents and chemotherapy, 55(10), 4606–4612. https://doi.org/10.1128/AAC.00714-11.spa
dc.relation.referencesLebreton, F., Willems, R.J.L., Gilmore, M.S., Lebreton, F., Willems, R.J.L. (2014). Enterococcus diversity, origins in nature, and gut colonization. In Gilmore MS, Clewell DB, Ike Y, Shankar N (ed), Enterococci: from commensals to leading causes of drug resistant infection. Massachusetts Eye and Ear Infirmary, Boston, MA: http://www.ncbi.nlm.nih.gov/books/NBK190427/.spa
dc.relation.referencesLionel Rigottier-Gois, Clément Madec, Albertas Navickas, Renata C. Matos, Elodie Akary-Lepage, Michel-Yves Mistou, Pascale Serror. (2015). The Surface Rhamnopolysaccharide Epa of Enterococcus faecalis Is a Keyspa
dc.relation.referencesLiu Y, Cao B, Gu L, Wang H. Molecular characterization of vancomycinresistant enterococci in a Chinese hospital between 2003 and 2009. Microb Drug Resist. 2011; 17:449–455.spa
dc.relation.referencesLópez-Luis, B.A., Sifuentes-Osornio, J., Lambraño-Castillo, D., Ortiz Brizuela, E., Ramírez-Fontes, A., Tovar-Calderón, Y.E., Leal-Vega, F.J., Bobadilla-del-Valle, M., Ponce-de-León, A. (2021). Risk factors and outcomes associated with vancomycin-resistant Enterococcus faecium and ampicillin-resistant Enterococcus faecalis bacteraemia: A 10-year study in a tertiary-care centre in Mexico City. Journal of Global Antimicrobial Resistance,24,198-204. https://doi. org/10.1016/j.jgar.2020.12.005.spa
dc.relation.referencesMadsen, K. T., Skov, M. N., Gill, S., & Kemp, M. (2017). Virulence Factors Associated with Enterococcus Faecalis Infective Endocarditis: A Mini Review. The open microbiology journal, 11, 1–11. https://doi.org/10.2174/1874285801711010001.spa
dc.relation.referencesMagill, S. S., Dumyati, G., Ray, S. M., & Fridkin, S. K. (2015). Evaluating Epidemiology and Improving Surveillance of Infections Associated with Health Care, United States. Emerging infectious diseases, 21(9), 1537–1542. https://doi. org/10.3201/eid2109.150508.spa
dc.relation.referencesManassero, N.C., Navarro, M., Rocchi, M., di Bella, H., Gasparotto, A.M., Ocaña, Carrizo, A.V., Novillo, F., Furiasse, D., Monterisi, A. (2016). Análisis de 117 episodios de bacteriemia por enterococo: estudio de la epidemiología, microbiología y sensibilidad a los antimicrobianos. Revista Argentina de Microbiología, 48(4),298-302.spa
dc.relation.referencesManson, J.M., Hancock, L.E., Gilmore, M.S. (2010). Mechanism of chromosomal transfer of Enterococcus faecalis pathogenicity island, capsule, antimicrobial resistance, and other traits. Proceedings of the National Academy of Sciences of the United States of America, 107(27,: 12269-74.spa
dc.relation.referencesMendes, R.E., Hogan, P.A., Streit, J.M., Jones, R.N., Flamm, R.K. (2014). Zyvox annual appraisal of potency and spectrum (ZAAPS) program: report of linezolid activity over 9 years (2004–12). Journal of Antimicrobial Chemotherapy, 69,582-1588.spa
dc.relation.referencesMeziane-Cherif, D., Saul, F. A., Haouz, A., & Courvalin, P. (2012). Structural and functional characterization of VanG D-Ala:D-Ser ligase associated with vancomycin resistance in Enterococcus faecalis. The Journal of biological chemistry, 287(45), 37583–37592. https://doi.org/10.1074/jbc.M112.405522.spa
dc.relation.referencesMeziane-Cherif, D., Stogios, P.J., Evdokimova, E., Savchenko, A., Courvalin P. (2014). Evolution of vancomycin resistance d,d-peptidases. Proceedings of the National Academy of Sciences,111 (16), 5872-5877.spa
dc.relation.referencesMikalsen, T., Pedersen, T., Willems, R., Coque, T.M., Werner, G., Sadowy, E., van Schaik, W., Jensen, L.B., Sundsfjord, A., Hegstad, K. (2015). Investigating the mobilome in clinically important lineages of Enterococcus faecium and Enterococcus faecalis. BMC Genomics,16,282.spa
dc.relation.referencesMiller, W. R., Munita, J. M., & Arias, C. A. (2014). Mechanisms of antibiotic resistance in enterococci. Expert review of anti-infective therapy, 12(10), 1221– 1236. https://doi.org/10.1586/14787210.2014.956092.spa
dc.relation.referencesMishra, N. N., Bayer, A. S., Tran, T. T., Shamoo, Y., Mileykovskaya, E., Dowhan, W., Guan, Z., & Arias, C. A. (2012). Daptomycin resistance in enterococci is associated with distinct alterations of cell membrane phospholipid content. PloS one, 7(8), e43958. https://doi.org/10.1371/journal.pone.0043958spa
dc.relation.referencesMohamed, O.A., Keith, E. (2018). Vancomycin-Resistant Enterococci: A Review of Antimicrobial Resistance Mechanisms and Perspectives of Human and Animal Health Baptiste.Microbial Drug Resistance, 24(5),590-606. https://doi. org/10.1089/mdr.2017.0147spa
dc.relation.referencesMoon, T. M., D’Andréa, É. D., Lee, C. W., Soares, A., Jakoncic, J., Desbonnet, C., Garcia-Solache, M., Rice, L. B., Page, R., & Peti, W. (2018). The structures of penicillin-binding protein 4 (PBP4) and PBP5 from Enterococci provide structural insights into -lactam resistance. The Journal of biological chemistry, 293(48), 18574–18584. https://doi.org/10.1074/jbc.RA118.006052.spa
dc.relation.referencesMoure, Z., Lara, N., Marín, M., Sola-Campoy, P.J., Bautista, V., GómezBertomeu, F., Gómez-Dominguez, C., Pérez-Vázquez, M., Aracil, B., Campos, J., Cercenado, E., Oteo-Iglesias, J. (2020). Spanish LinezolidResistant Enterococci Collaborating Group. Interregional spread in Spain of linezolid-resistant Enterococcus spp. isolates carrying the optrA and poxtA genes. International Journal of Antimicrobial Agents,55(6),105977.spa
dc.relation.referencesNeumann, B., Prior, K., Bender, J. K., Harmsen, D., Klare, I., Fuchs, S., Bethe, A., Zühlke, D., Göhler, A., Schwarz, S., Schaffer, K., Riedel, K., Wieler, L. H., & Werner, G. (2019). A Core Genome Multilocus Sequence Typing Scheme for Enterococcus faecalis. Journal of clinical microbiology, 57(3), e01686-18. https://doi. org/10.1128/JCM.01686-18.spa
dc.relation.referencesNunez, N., Derré-Bobillot, A., Gaubert, S, Herry, J-M., Deschamps, J., Wei, Y., Baranek, T., Si-Tahar, M., Briandet, R., Serror, P., Archambaud, C. (2018). Exploration of the role of the virulence factor ElrA during Enterococcus faecalis cell infection. Scientific Reports, 8, 1749 https://doi.org/10.1038/s41598-018- 20206-6.spa
dc.relation.referencesOcvirk, S., Sava, I.G., Lengfelder, I., Lagkouvardos, I., Steck, N., Roh, J.H., Tchaptchet, S., Bao, Y., Hansen, J.J., Huebner, J., Carroll, I.M., Murray, B.E., Sartor, R.B., Haller, D. (2015). Surface-Associated Lipoproteins Link Enterococcus faecalis Virulence to Colitogenic Activity in IL-10-Deficient Mice Independent of Their Expression Levels. PLOS Pathogens, 11(6),e1004911. doi: 10.1371/journal. ppat.1004911.spa
dc.relation.referencesO’Driscoll, T., & Crank, C. W. (2015). Vancomycin-resistant enterococcal infections: epidemiology, clinical manifestations, and optimal management. Infection and drug resistance, 8, 217–230. https://doi.org/10.2147/IDR.S54125.spa
dc.relation.referencesOlawale, K. O., Fadiora, S. O., & Taiwo, S. S. (2011). Prevalence of hospitalacquired enterococci infections in two primary-care hospitals in osogbo, southwestern Nigeria. African journal of infectious diseases, 5(2), 40–46. https://doi. org/10.4314/ajid.v5i2.66513.spa
dc.relation.referencesPadmasini, E., Padmaraj, R., & Ramesh, S. S. (2014). High level aminoglycoside resistance and distribution of aminoglycoside resistant genes among clinical isolates of Enterococcus species in Chennai, India. The Scientific World Journal, 2014, 329157. https://doi.org/10.1155/2014/329157.spa
dc.relation.referencesPadmasini, E., Padmaraj, R., Srivani, S. (2014) High Level Aminoglycoside Resistance and Distribution of Aminoglycoside Resistant Genes among Clinical Isolates of Enterococcus Species in Chennai, India”, The Scientific World Journal, 2014, Article ID 329157. https://doi.org/10.1155/2014/329157.spa
dc.relation.referencesPalmer, K. L., Daniel, A., Hardy, C., Silverman, J., & Gilmore, M. S. (2011). Genetic basis for daptomycin resistance in enterococci. Antimicrobial agents and chemotherapy, 55(7), 3345–3356. https://doi.org/10.1128/AAC.00207-11.spa
dc.relation.references.Palmer, K.L., Gilmore, M.S. (2010). Multidrug-Resistant Enterococci Lack CRISPR-cas. MBi., 1(4), e00227-10. http://mbio.asm.org/content/1/4/e00227- 10.short?rss=1&ssource=mfc.spa
dc.relation.referencesPfaller, M. A., Cormican, M., Flamm, R. K., Mendes, R. E., & Jones, R. N. (2019). Temporal and Geographic Variation in Antimicrobial Susceptibility and Resistance Patterns of Enterococci: Results From the SENTRY Antimicrobial Surveillance Program, 1997-2016. Open forum infectious diseases, 6(Suppl 1), S54– S62. https://doi.org/10.1093/ofid/ofy344.spa
dc.relation.referencesPogliano, J., Pogliano, N., & Silverman, J. A. (2012). Daptomycinmediated reorganization of membrane architecture causes mislocalization of essential cell division proteins. Journal of bacteriology, 194(17), 4494–4504. https://doi. org/10.1128/JB.00011-12.spa
dc.relation.referencesRaza, T., Ullah, S. R., Mehmood, K., & Andleeb, S. (2018). Vancomycin resistant Enterococci: A brief review. JPMA. The Journal of the Pakistan Medical Association, 68(5), 768–772.spa
dc.relation.referencesReyes, K., Malik, R., Moore, C., Donabedian, S., Perri, M., Johnson, L., & Zervos, M. (2010). Evaluation of risk factors for coinfection or cocolonization with vancomycin-resistant enterococcus and methicillinresistant Staphylococcus aureus. Journal of clinical microbiology, 48(2), 628–630. https://doi.org/10.1128/ JCM.02381-08.spa
dc.relation.referencesRodríguez-Niklitschek, C., Oporto, G.H. (2015). Implicancias clínicas de la contaminación microbiana por Enterococcus faecalis en canales radiculares de dientes desvitalizados: Revisión de la literatura. Revista Odontológica Mexicana,19(3),181-186.spa
dc.relation.referencesSaavedra, S. Y., Bernal, J. F., Montilla-Escudero, E., Torres, G., Rodríguez, M. K., Hidalgo, A. M., Ovalle, M. V., Rivera, S., Perez-Gutierrez, E., & Duarte, C. (2020). Vigilancia nacional de aislamientos clínicos de Enterococcus faecalis resistentes al linezolid portadores del gen optrA en Colombia, 2014-2019 [National surveillance of clinical isolates of Enterococcus faecalis resistant to linezolid carrying the optrA gene in Colombia, 2014-2019]. Revista panamericana de salud publica = Pan. American journal of public health, 44, e104. https://doi. org/10.26633/RPSP.2020.104spa
dc.relation.referencesSader, H.S., Farrell, D.J., Flamm, R.K., Jones, R.N.(2014). Daptomycin activity tested against 164457 bacterial isolates from hospitalised patients: summary of 8 years of a Worldwide Surveillance Programme (2005-2012). International Journal of Antimicrobial Agents,43(5),465-9.spa
dc.relation.referencesSalipante, S. J., SenGupta, D. J., Cummings, L. A., Land, T. A., Hoogestraat, D. R., & Cookson, B. T. (2015). Application of whole-genome sequencing for bacterial strain typing in molecular epidemiology. Journal of clinical microbiology, 53(4), 1072–1079. https://doi.org/10.1128/JCM.0338514}.spa
dc.relation.referencesSchell, C. M., Tedim, A. P., Rodríguez-Baños, M., Sparo, M. D., Lissarrague, S., Basualdo, J. A., & Coque, T. M. (2020). Detection of Lactamase-Producing Enterococcus faecalis and Vancomycin-Resistant Enterococcus faecium Isolates in Human Invasive Infections in the Public Hospital of Tandil, Argentina. Pathogens (Basel, Switzerland), 9(2), 142. https://doi.org/10.3390/pathogens9020142.spa
dc.relation.referencesShariati, A., Dadashi, M., Chegini, Z., van Belkum, A., Mirzaii, M., Khoramrooz, S. S., & Darban-Sarokhalil, D. (2020). The global prevalence of Daptomycin, Tigecycline, Quinupristin/Dalfopristin, and Linezolid-resistant Staphylococcus aureus and coagulase-negative staphylococci strains: a systematic review and meta-analysis. Antimicrobial resistance and infection control, 9(1), 56. https://doi. org/10.1186/s13756-020-00714-9.spa
dc.relation.referencesSharifzadeh, V., Mohabati, A., Shahcheraghi F., Khoramabadi, N., Razaz, N., Hosseini, R. (2020). High-level aminoglycoside resistance and distribution of aminoglycoside resistance genes among Enterococcus spp. clinical isolates in Tehran, Iran. Journal of Global Antimicrobial Resistance, 20,318-32.https://doi. org/10.1016/j.jgar.2019.08.008.spa
dc.relation.referencesShen, J., Wang, Y., Schwarz, S. (2013). Presence and dissemination of the multiresistance gene cfr in Gram-positive and Gram-negative bacteria. Journal of Antimicrobial Chemotherapy, 68,1697–1706.spa
dc.relation.referencesShiga, H., Kajiura, T., Shinozaki, J., Takagi, S., Kinouchi, Y., Takahashi, S., Negoro, K., Endo, K., Kakuta, Y., Suzuki, M., Shimosegawa, T. (2012). Changes of faecal microbiota in patients with Crohn’s disease treated with an elemental diet and total parenteral nutrition. Digestive and Liver Disease, 44,736–42.spa
dc.relation.referencesShutter MC, Akhondi H. (2021).Tetracycline. In: StatPearls. Treasure Island (FL): StatPearls Publishing; 2021 Jan-. Available from: https://www.ncbi.nlm.nih.gov/ books/NBK549905.spa
dc.relation.referencesSidle,r J.A., Battegay, M., Tschudin-Sutter, S., Widmer, A.F., Weisser, M. (2014). Enterococci, Clostridium difficile and ESBL-producing bacteria: epidemiology, clinical impact and prevention in ICU patients. Swiss Medical Weekly,144,w14009.spa
dc.relation.referencesSilva N, Igrejas G, Gonçalves A, Poeta P. 2011. Commensal gut bacteria: distribution of Enterococcus species and prevalence of Escherichia coli phylogenetic groups in animals and humans in Portugal. Ann Microbiol 62:449–459. doi:10.1007/ s13213-011-0308-4.spa
dc.relation.referencesSilva, J., Rodríguez, Y., Araya, J., Gahona, J., Valenzuela, N., Guerrero, K., Báez, J., Baquero, F., del Campo, R. (2013). Detección de genes de virulencia en cepas de Enterococcus faecalis susceptibles y resistentes a aminoglucósidos. Revista chilena de infectología, 30(1), 17-22. https://dx.doi.org/10.4067/S0716- 10182013000100003.spa
dc.relation.referencesSilva, J., Rodríguez, Y., Araya, J., Gahona, J., Valenzuela, N., Guerrero, K., Báez, J., Baquero, F., del Campo, Rosa. (2013). Detección de genes de virulencia en cepas de Enterococcus faecalis susceptibles y resistentes a aminoglucósidos. Revista chilena de infectología, 30(1), 17-22. https://dx.doi.org/10.4067/S0716- 10182013000100003.spa
dc.relation.referencesStogios, P.J., Savchenko, A. (2020). Molecular mechanisms of vancomycin resistance. Protein Science, 29(3),654-669.spa
dc.relation.referencesSun, H., Wang, H., Xu, Y., Jones, R.N., Costello, A.J., Liu, Y., Li, G., Chen, M., Mendes, R.E. (2012). Molecular characterization of vancomycinresistant Enterococcus spp. clinical isolates recovered from hospitalized patients among several medical institutions in China. Diagnostic Microbiology and Infectious Disease,74(4),399-403.spa
dc.relation.referencesTaglialegna, A., Matilla-Cuenca, L., Dorado-Morales, P., Navarro, Susanna., Ventura, S., Garnett, J.A., Lasa, I., Valle, J. (2020). The biofilmassociated surface protein Esp of Enterococcus faecalis forms amyloid-like fibers. npj Biofilms Microbiomes, 6, 15 https://doi.org/10.1038/s41522-0200125-2.spa
dc.relation.referencesTedim, A. P., Ruiz-Garbajosa, P., Corander, J., Rodríguez, C. M., Cantón, R., Willems, R. J., Baquero, F., & Coque, T. M. (2015). Population biology of intestinal enterococcus isolates from hospitalized and nonhospitalized individuals in different age groups. Applied and environmental microbiology, 81(5), 1820–1831. https://doi.org/10.1128/AEM.03661-14.spa
dc.relation.referencesThaker, M., Spanogiannopoulos, P., Wright, G.D. (2010). The tetracycline resistome. Cellular and Molecular Life Sciences,67,419–31.spa
dc.relation.referencesThurlow, L. R., Thomas, V. C., Narayanan, S., Olson, S., Fleming, S. D., & Hancock, L. E. (2010). Gelatinase contributes to the pathogenesis of endocarditis caused by Enterococcus faecalis. Infection and immunity, 78(11), 4936–4943. https://doi. org/10.1128/IAI.01118-09.spa
dc.relation.referencesTian, Y., Yu, H. & Wang, Z. (2019). Distribution of acquired antibiotic resistance genes among Enterococcus spp. isolated from a hospital in Baotou, China. BMC Research Notes,12, 27. https://doi.org/10.1186/s13104-019-4064-z.spa
dc.relation.referencesTran, T. T., Panesso, D., Gao, H., Roh, J. H., Munita, J. M., Reyes, J., Diaz, L., Lobos, E. A., Shamoo, Y., Mishra, N. N., Bayer, A. S., Murray, B. E., Weinstock, G. M., & Arias, C. A. (2013). Whole-genome analysis of a daptomycin-susceptible Enterococcus faecium strain and its daptomycinresistant variant arising during therapy. Antimicrobial agents and chemotherapy, 57(1), 261–268. https://doi. org/10.1128/AAC.01454-12.spa
dc.relation.referencesVan Schaik, W., Willems, R.J.L. (2010). Genome-based insights into the evolution of enterococci. Clinical Microbiology and Infection, 16,527–532. doi:10.1111/j.1469- 0691.2010.03201.x.spa
dc.relation.referencesVan Tyne, D., & Gilmore, M. S. (2014). Friend turned foe: evolution of enterococcal virulence and antibiotic resistance. Annual review of microbiology, 68, 337–356. https://doi.org/10.1146/annurev-micro-091213113003.spa
dc.relation.referencesVan Tyne, D., & Gilmore, M.S. (2014). Friend turned foe: evolution of enterococcal virulence and antibiotic resistance. Annual review of microbiology, 68, 337– 356. https://doi.org/10.1146/annurev-micro-091213113003.spa
dc.relation.referencesVesi, D., Kristich, C. (2012). JMurAA is required for intrinsic cephalosporin resistance of Enterococcus faecalis. Antimicrobial agents and chemotherapy, 56(5), 2443–2451. https://doi.org/10.1128/AAC.05984-11.spa
dc.relation.referencesVolkers, G., Damas, J.M., Palm, G.J., Panjikar, S., Soares, C.M., Hinrichs, W. (2013). Putative dioxygen-binding sites and recognition of tigecycline and minocycline in the tetracycline degrading monooxygenase TetX. Acta Crystallographica Section D,69, 1758–67.spa
dc.relation.referencesWang, J.S., Muzevich, K., Edmond, M.B., Bearman, G., Stevens, M.P. (2014). Central nervous system infections due to vancomycin-resistant enterococci: case series and review of the literature. International Journal of Infectious Diseases, 25.26–31.spa
dc.relation.referencesWang, Y., Lv, Y., Cai, J., Schwarz, S., Cui, L., Hu, Z., Z., Rong, L., Jun, Z., Qin, H., Tao, W., Dacheng, W., Zheng, S., Yingbo, L., Feßler, A.T., Wu, C., Yu, H., Deng, X., Xia, X., Shen, J. (2015). A novel gene, optrA, that confers transferable resistance to oxazolidinones and phenicols and its presence in Enterococcus faecalis and Enterococcus faecium of human and animal origin, Journal of Antimicrobial Chemotherapy, 70(8),2182–2190. https://doi.org/10.1093/jac/dkv116.spa
dc.relation.referencesWeiner, L. M., Webb, A. K., Limbago, B., Dudeck, M. A., Patel, J., Kallen, A. J., Edwards, J. R., & Sievert, D. M. (2016). Antimicrobial-Resistant Pathogens Associated With Healthcare-Associated Infections: Summary of Data Reported to the National Healthcare Safety Network at the Centers for Disease Control and Prevention, 2011-2014. Infection control and hospital epidemiology, 37(11), 1288– 1301. https://doi.org/10.1017/ice.2016.174spa
dc.relation.referencesXu, X., Lin, D., Yan, G., Ye, X., Wu, S., Guo, Y., Zhu, D., Hu, F., Zhang, Y., Wang, F., Jacoby, G. A., & Wang, M. (2010). vanM, a new glycopeptide resistance gene cluster found in Enterococcus faecium. Antimicrobial agents and chemotherapy, 54(11), 4643–4647. https://doi.org/10.1128/AAC.0171009.spa
dc.relation.referencesYeong Bin Kim, Kwang Won Seo, Hye Young Jeon, Suk-Kyung Lim, Haan Woo Sung, Young Ju Lee. (2019). Molecular characterization of erythromycin and tetracycline-resistant Enterococcus faecalis isolated from retail chicken meats, Poultry Science, 98(2),977-983.spa
dc.relation.referencesYou-Han, C., Shang-Yi, L., Yu-Tzu, L., Sung-Pin, T., Chen-Chia, C,Song-Yih, Y., WeiWen, H,, Ya-Ting, J,, Chun-Yu, L,, Yen-Hsu, C., Wei-Chun, H. (2021). Emergence of aac(6)-Ie-aph(2)-Ia-positive enterococci with non-high-level gentamicin resistance mediated by IS1216V: adaptation to decreased aminoglycoside usage in Taiwan, Journal of Antimicrobial Chemotherapy, 76(7),1689–1697, https://doi. org/10.1093/jac/dkab071.spa
dc.relation.references.Zhang, T., Muraih, J.K., Mintzer, E., Tishbi, N., Desert, C., Silverman, J., Taylor, S., Palme,r M. (2013). Mutual inhibition through hybrid oligomer formation of daptomycin and the semisynthetic lipopeptide antibiotic CB182,462. Biochimica et Biophysica Acta,1828(2),302-8.spa
dc.relation.referencesZischka, M., Künne, C. T., Blom, J., Wobser, D., Sak nç, T., SchmidtHohagen, K., Dabrowski, P. W., Nitsche, A., Hübner, J., Hain, T., Chakraborty, T., Linke, B., Goesmann, A., Voget, S., Daniel, R., Schomburg, D., Hauck, R., Hafez, H. M., Tielen, P., Jahn, D., Werner, G. (2015). Comprehensive molecular, genomic and phenotypic analysis of a major clone of Enterococcus faecalis MLST ST40. BMC genomics, 16(1), 175. https://doi.org/10.1186/s12864-015-1367-xspa
dc.relation.referencesAbdullahi, I. N., Lozano, C., Ruiz-Ripa, L., Fernández-Fernández, R., Zarazaga, M., & Torres, C. (2021). Ecology and Genetic Lineages of Nasal Staphylococcus aureus and MRSA Carriage in Healthy Persons with or without Animal-Related Occupational Risks of Colonization: A Review of Global Reports. Pathogens (Basel, Switzerland), 10(8), 1000.spa
dc.relation.referencesBallhausen, B., Kriegeskorte, A., Schleimer, N., Peters, G., & Becker, K. (2014). The mecA homolog mecC confers resistance against -lactams in Staphylococcus aureus irrespective of the genetic strain background. Antimicrobial agents and chemotherapy, 58(7), 3791–3798.spa
dc.relation.referencesBeam, J.W., Buckley, B. (2006). Community-acquired methicillin-resistant Staphylococcus aureus: prevalence and risk factors. Journal of Athletic Training,; 41, 337-40.spa
dc.relation.referencesBettin, A., Causil, C., Reyes, N. (2012). Molecular identification and antimicrobial susceptibility of Staphylococcus aureus nasal isolates from medical students in Cartagena, Colombia. Brazilian Journal of Infectious Diseases,16(4),329–334.spa
dc.relation.referencesCastro, R.,Villafañe, L.M., Álvarez, E., Martínez, M., Rambaut, C., Vitola, G. (2010). Methicillin-resistant Staphylococcus aureus in children attending school in Cartagena, Colombia. Salud Pública,12(3),454-463spa
dc.relation.referencesChen, C.S., Chen, C.Y., Huang, Y.C. (2012). Nasal carriage rate and molecular epidemiology of methicillin-resistant Staphylococcus aureus among medical students at a Taiwanese university. International Journal of Infectious Diseases, 16, e799–e803.spa
dc.relation.referencesClinical and Laboratory Standards Institute. (2015). Performance Standards for Antimicrobial Susceptibility Testing: Twenty-Fifth Informational Supplement.; M100-S25. CLSI, Wayne, PA, USA.spa
dc.relation.referencesDanelli, T., Duarte, F. C., de Oliveira, T. A., da Silva, R. S., Frizon Alfieri, D., Gonçalves, G. B., de Oliveira, C. F., Tavares, E. R., Yamauchi, L. M., Perugini, M., & Yamada-Ogatta, S. F. (2020). Nasal Carriage by Staphylococcus aureus among Healthcare Workers and Students Attending a University Hospital in Southern Brazil: Prevalence, Phenotypic, and Molecular Characteristics. Interdisciplinary perspectives on infectious diseases, 2020, 3808036.spa
dc.relation.referencesEscobar, J. A., Márquez-Ortiz, R. A., Álvarez-Olmos, M. I., Leal, A. L., Castro, B. E., Vanegas, N., & Research Group of Pediatric Infectious Diseases (2013). Detection of a new community genotype methicillin-resistant Staphylococcus aureus clone that is unrelated to the USA300 clone and that causes pediatric infections in Colombia. Journal of clinical microbiology, 51(2), 661–664.spa
dc.relation.referencesEscobar-Pérez, J., Reyes, N., Márquez-Ortiz, R. A., Rebollo, J., Pinzón, H., Tovar, C., Moreno-Castañeda, J., Corredor, Z. L., Castro, B. E., Moncada, M. V., & Vanegas, N. (2017). Emergence and spread of a new communitygenotype methicillinresistant Staphylococcus aureus clone in Colombia. BMC infectious diseases, 17(1), 108.spa
dc.relation.referencesFergestad, M. E., Stamsås, G. A., Morales Angeles, D., Salehian, Z., Wasteson, Y., & Kjos, M. (2020). Penicillin-binding protein PBP2a provides variable levels of protection toward different -lactams in Staphylococcus aureus RN4220. MicrobiologyOpen, 9(8), e1057.spa
dc.relation.referencesFigueiredo, A. M., & Ferreira, F. A. (2014). The multifaceted resources and microevolution of the successful human and animal pathogen methicillinresistant Staphylococcus aureus. Memorias do Instituto Oswaldo Cruz, 109(3), 265–278.spa
dc.relation.referencesFortaleza, C.R., Melo, E.C., Fortaleza, C.M.C.B. (2009). Colonización nasal por el Staphylococcus aureus resistente a la meticilina y mortalidad en pacientes de una unidad de terapia intensiva. Revista Latino-Americana de Enfermagem,17(5), www.eerp.usp.br/rlae.spa
dc.relation.referencesGaona, M.A., Chaparro, D.I., Peña, M.C., Pineda, A.C., Ibáñez, M., Ramírez, G. (2009). Variacion del estado de portador de Staphylococcus aureus en una población de estudiantes de medicina. Revista Ciencias de la Salud, 7(1),37-46.spa
dc.relation.referencesHawkins, G., Stewart, S., Blatchford, O., Reilly, J. (2011). Should healthcare workers be screened routinely for meticillin-resistant Staphylococcus aureus? A review of the evidence. Journal of Hospital Infection, 77(4),285–9.spa
dc.relation.referencesHidalgo, M., Carvajal, L. P., Rincón, S., Faccini-Martínez, Á. A., Tres Palacios, A. A., Mercado, M., Palomá, S. L., Rayo, L. X., Acevedo, J. A., Reyes, J., Panesso, D., García-Padilla, P., Álvarez, C., & Arias, C. A. (2015). Methicillin-Resistant Staphylococcus aureus USA300 Latin American Variant in Patients Undergoing Hemodialysis and HIV Infected in a Hospital in Bogotá, Colombia. PloS one, 10(10), e0140748.spa
dc.relation.referencesIto, T., Y. Katayama, K. Asada, N. Mori, K. Tsutsumimoto, C. Tiensasitorn, and K. Hiramatsu. (2001). Structural comparison of three types of staphylococcal cassette chromosome mec integrated in the chromosome in methicillin-resistant Staphylococcus aureus. Antimicrob. Agents Chemother,45,1323–1336.spa
dc.relation.referencesKirecci, E., Ozer, A., Ara,l M., Miraloglu, M. A (2010). Research of nasal methicillin resistant/sensitive Staphylococcus aureus and pharyngeal betahaemolytic Streptococcus carriage in midwifery students in Kahramanmaras, Eastern Mediterranean Region of Turkey. Ethiopian Journal of Health Development,24(1),57-60spa
dc.relation.referencesKitti, T., Boonyonying, K., Sitthisak, S. (2011). Prevalence of methicillinresistant Staphylococcus aureus among university students in Thailand. Southea Sta Sian. Journal of Tropical Medicine and Public Health, 42(6),1498-1504.spa
dc.relation.referencesLópez-Aguilera, S., Goñi-Yeste, M.M., Barrado, L., González-RodríguezSalinas, M.C., Otero, J.R., Chaves, F.(2013). Staphylococcus aureus nasal colonization in medical students: Importance in nosocomial transmission. Enfermedades Infecciosas y Microbiología Clínica, 31(8),500–505.spa
dc.relation.referencesMachuca, M. A., Sosa, L. M., & González, C. I. (2013). Molecular typing and virulence characteristic of methicillin-resistant Staphylococcus aureus isolates from pediatric patients in Bucaramanga, Colombia. PloS one, 8(8), e73434.spa
dc.relation.referencesMahmoud, A. M., Albadawy, H. S., Bolis, S. M., Bilal, N. E., Ahmed, A. O., & Ibrahim, M. E. (2015). Inducible clindamycin resistance and nasal carriage rates of Staphylococcus aureus among healthcare workers and community members. African health sciences, 15(3), 861–867.spa
dc.relation.referencesMartínez-Díaz, H. C., Valderrama-Beltrán, S. L., Hernández, A. C., Pinedo, S. K., Correa, J. R., Ríos, É. G., Rojas, J. J., Hernández, Y. Y., & Hidalgo, M. (2020). Methicillin-resistant Staphylococcus aureus nasal colonization in cardiovascular surgery patients at a university hospital in Bogotá, Colombia. Colonización nasal por Staphylococcus aureus resistente a la meticilina en pacientes sometidos a cirugía cardiovascular en un hospital universitario de Bogotá, Colombia. Biomedica : revista del Instituto Nacional de Salud, 40(Supl. 1), 37–44.spa
dc.relation.referencesMéndez, I.A., HolguÍn-Riaño, D.F., Pachón-Barinas, D.P., Africano, F.J., González, I.M., Rojas, N.A. (2013). Prevalence and antimicrobial susceptibility of Staphylococcus aureus methicilin resistant isolated from medical students. Revista CES de Medicina,27(1),21-30.spa
dc.relation.referencesOura, J.P., Pimenta, F.C., Hayashida, M., Cruz, E.D.A., Canini, S.R.M.S., Gir, E. (2011). La colonización de los profesionales de enfermería por Staphylococcus aureus. Revista Latino-Americana de Enfermagem, 19(2):08spa
dc.relation.referencesPopovich, K. J., Green, S. J., Okamoto, K., Rhee, Y., Hayden, M. K., Schoeny, M., Snitkin, E. S., & Weinstein, R. A. (2021). MRSA Transmission in Intensive Care Units: Genomic Analysis of Patients, Their Environments, and Healthcare Workers. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 72(11), 1879–1887.spa
dc.relation.referencesSakr, A., Brégeon, F., Mège, J. L., Rolain, J. M., & Blin, O. (2018). Staphylococcus aureus Nasal Colonization: An Update on Mechanisms, Epidemiology, Risk Factors, and Subsequent Infections. Frontiers in microbiology, 9, 2419.spa
dc.relation.referencesSlifka, K.J., Nettleman, M.D., Dybas, L., Stein, G.E. (2009). Is Acquisition of Methicillin- Resistant Staphylococcus aureus an Occupational Hazard for Medical Students? .Clinical Infectious Diseases,49,482–3.spa
dc.relation.referencesTokue, Y., Shoji, S., Satoh, K., Watanabe, A., & Motomiya, M. (1992). Comparison of a polymerase chain reaction assay and a conventional microbiologic method for detection of methicillin-resistant Staphylococcus aureus. Antimicrobial agents and chemotherapy, 36(1), 6–9.spa
dc.relation.referencesTong, S. Y., Davis, J. S., Eichenberger, E., Holland, T. L., & Fowler, V. G., Jr (2015). Staphylococcus aureus infections: epidemiology, pathophysiology, clinical manifestations, and management. Clinical microbiology reviews, 28(3), 603–661spa
dc.relation.referencesTrépanier, P., Tremblay, C., Ruest, A. (2013). Methicillin-resistant Staphylococcus aureus colonization among medical residents. Canadian Journal of Infectious Diseases and Medical Microbiology, 24(2),39-41.spa
dc.relation.referencesVelásquez, L.A., Sánchez, D.M., Hernández, O., González, L., Duque, C. (2010). Colonización por Staphylococcus aureus en una población de pacientes VIH positivos de la ciudad de Medellín: perfil de sensibilidad antimicrobiana y caracterización de la resistencia a la meticilina. Revista NOVA, 8(14), 121-240spa
dc.relation.referencesWulf, M., van Nes, A., Eikelenboom-Boskamp, A., de Vries, J., Melchers, W., Klaassen, C., & Voss, A. (2006). Methicillin-resistant Staphylococcus aureus in veterinary doctors and students, the Netherlands. Emerging infectious diseases, 12(12), 1939–1941.spa
dc.relation.referencesBalaban, N.Q., Gerdes, K., Lewis, K., McKinney, J.D (2013). A problem of persistence: still more questions than answers? Nature Reviews Microbiology,11, 587–591spa
dc.relation.referencesBarbier, F., Andremont, A., Wolff, M., Bouadma, L. (2013). Hospitalacquired pneumonia and ventilator-associated pneumonia: recent advances in epidemiology and management. Current Opinion in Pulmonary Medicine, 19, 216–228spa
dc.relation.referencesBhagirath, A. Y., Li, Y., Somayajula, D., Dadashi, M., Badr, S., & Duan, K. (2016). Cystic fibrosis lung environment and Pseudomonas aeruginosa infection. BMC pulmonary medicine, 16(1), 174.spa
dc.relation.referencesBlanc, D.S., Petignat, C., Moreillon, P., Wenger, A., Bille, J., Francioli, P. (1999). Quantitative antibiogram as a typing method for the prospective epidemiological surveillance and control of MRSA: comparison with molecular typing. Infection Control & Hospital Epidemiology, 17(10),654-69.spa
dc.relation.referencesBreidenstein, E.B., de la Fuente-Núñez, C., Hancock, R. (2011). Pseudomonas aeruginosa: all roads lead to resistance. Trends in Microbiology,19,419–426.spa
dc.relation.referencesClinical and Laboratory Standards Institute (CLSI). (2015). Performance standards for antimicrobial susceptibility testing; 25th informational supplement. CLSI M100-S25 Clinical and Laboratory Standards Institute, Wayne, PAspa
dc.relation.referencesCorrea, A., Del Campo, R., Perenguez, M., Blanco, V. M., RodríguezBaños, M., Perez, F., Maya, J. J., Rojas, L., Cantón, R., Arias, C. A., & Villegas, M. V. (2015). Dissemination of high-risk clones of extensively drug-resistant Pseudomonas aeruginosa in colombia. Antimicrobial agents and chemotherapy, 59(4), 2421–2425.spa
dc.relation.referencesCorrea, A., Montealegre, M. C., Mojica, M. F., Maya, J. J., Rojas, L. J., De La Cadena, E. P., Ruiz, S. J., Recalde, M., Rosso, F., Quinn, J. P., & Villegas, M. V. (2012). First report of a Pseudomonas aeruginosa isolate coharboring KPC and VIM carbapenemases. Antimicrobial agents and chemotherapy, 56(10), 5422–5423.spa
dc.relation.referencesCortes, J.A., Leal, A.L., Montañez, A.M., Buitrago, G., Castillo, J.S., Guzman, L. (2013). Frequency of microorganisms isolated in patients with bacteremia in intensive care units in Colombia and their resistance profiles”, Brazilian Journal of Infectious Diseases,17,346–52.spa
dc.relation.referencesCuzon, G., Naas, T., Villegas, M. V., Correa, A., Quinn, J. P., & Nordmann, P. (2011). Wide dissemination of Pseudomonas aeruginosa producing beta-lactamase blaKPC-2 gene in Colombia. Antimicrobial agents and chemotherapy, 55(11), 5350–5353.spa
dc.relation.referencesGales, A., Castanheira, M., Jones, R., Sader, H. (2012). Antimicrobial resistance among Gram-negative bacilli isolated from Latin America: Results from SENTRY Antimicrobial Surveillance Program (Latin America, 2008-2010). Diagnostic microbiology and infectious disease,73,354-60.spa
dc.relation.referencesHarris, A. D., Jackson, S. S., Robinson, G., Pineles, L., Leekha, S., Thom, K. A., Wang, Y., Doll, M., Pettigrew, M. M., & Johnson, J. K. (2016). Pseudomonas aeruginosa Colonization in the Intensive Care Unit: Prevalence, Risk Factors, and Clinical Outcomes. Infection control and hospital epidemiology, 37(5), 544–548.spa
dc.relation.referencesHirsch, E. B., & Tam, V. H. (2010). Impact of multidrug-resistant Pseudomonas aeruginosa infection on patient outcomes. Expert review of pharmacoeconomics & outcomes research, 10(4), 441–451.spa
dc.relation.referencesJeong, S.J., Yoon, S.S., Bae, I.K., Jeong, S.H., Kim, J.M., Lee, K. (2014). Risk factors for mortality in patients with bloodstream infections caused by carbapenemresistant Pseudomonas aeruginosa: clinical impact of bacterial virulence and strains on outcome. Diagnostic Microbiology and Infectious Disease,80(2),130-5.spa
dc.relation.referencesKovaleva, J., Peters, F. T., van der Mei, H. C., & Degener, J. E. (2013). Transmission of infection by flexible gastrointestinal endoscopy and bronchoscopy. Clinical microbiology reviews, 26(2), 231–254.spa
dc.relation.referencesLambert ML, Suetens C, Savey A, Palomar M, Hiesmayr M, Morales I, Agodi A, Frank,U., Mertens, K., Schumacher, M., Wolkewitz, M. (2011). Clinical outcomes of health-care-associated infections and antimicrobial resistance in patients admitted to European intensive-care units: a cohort study. The Lancet Infectious Diseases,11(1),30-8.spa
dc.relation.referencesMagiorakos, A.P., Srinivasan, A., Carey, R.B., Carmeli, Y., Falagas, M.E., Giske, C.G., Harbarth, S., Hindler, J.F., Kahlmeter, G., Olsson-Liljequist, B., Paterson, D.L., Rice, L.B., Stelling, J., Struelens, M.J., Vatopoulos, A., Weber, J.T., Monnet, D.L. (2012). Multidrug-resistant, extensively drugresistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistance. Clinical Microbiology and Infection,18, 268–281.spa
dc.relation.referencesMorales, E., Cots, F., Sala, M., Comas, M., Belvis, F., Riu, M., Salvadó, M., Grau, S., Horcajada, J.P., Montero, M.M., Castells, X. (2012). Hospital costs of nosocomial multi-drug resistant Pseudomonas aeruginosa acquisition. BMC Health Services Research,12,122.spa
dc.relation.referencesOliver, A., Mulet, X., López-Causapé, C., Juan, C. (2015). The increasing threat of Pseudomonas aeruginosa high-risk clones. Drug Resistance Updates,21–22,41–59.spa
dc.relation.referencesOtter, J., Yezli, S., & French, G. (2011). The Role Played by Contaminated Surfaces in the Transmission of Nosocomial Pathogens. Infection Control & Hospital Epidemiology, 32(7), 687-699.spa
dc.relation.referencesPalleroni, N.J. (2010). The Pseudomonas story. Environ. Microbiol, 12(6),1377-83.spa
dc.relation.referencesPeña, C. Cabot, G. Gómez-Zorrilla, S. Zamorano, L. Ocampo-Sosa, A.. Murillas, J, Spanish Network for Research in Infectious Diseases (REIPI). (2015). Influence of virulence genotype and resistance profile in the mortality of Pseudospa
dc.relation.referencesPoole, K. (2011). Pseudomonas aeruginosa: resistance to the max. Frontiers in microbiology,2,65.spa
dc.relation.referencesSalvador, G., García, L.R., Gonzales, E. (2018). Characterization of metallolactamase in clinical isolates of Pseudomonas aeruginosa retrieved from patients hospitalized in the Central Military Hospital. Revista Peruana de Medicina Experimental y Salud Pública, 35(4),636-641,spa
dc.relation.referencesTacconelli, E., Magrini, N., Carmeli, Y., Harbarth, S., Kahlmeter, G., Kluytmans, J., Mendelson, M., Pulcini, C., Singh, N., Theuretzbacher U. (2017). Global priority list of antibiotic-resistant bacteria to guide research, discovery, and development of new antibiotics. World Health Organization, 1-7.spa
dc.relation.referencesVanegas, J.M,. Cienfuegos, A.V., Ocampo, A.M., López, L., del Corral, H., Roncancio, G., Sierra, P., Echeverri-Toro, L., Ospina, S., Robledo, N.C., Restrepo, A., Jiménez, N. (2014). Similar Frequencies of Pseudomonas aeruginosa Isolates Producing KPC and VIM Carbapenemases in Diverse Genetic Clones at Tertiary-Care Hospitals in Medellín, Colombia, Journal of Clinical Microbiology, 52(11),3978–3986,spa
dc.relation.referencesWalters, M. S., Grass, J. E., Bulens, S. N., Hancock, E. B., Phipps, E. C., Muleta, D., Mounsey, J., Kainer, M. A., Concannon, C., Dumyati, G., Bower, C., Jacob, J., Cassidy, P. M., Beldavs, Z., Culbreath, K., Phillips, W. E., Jr, Hardy, D. J., Vargas, R. L., Oethinger, M., Ansari, U., … Kallen, A. (2019). Carbapenem-Resistant Pseudomonas aeruginosa at US Emerging Infections Program Sites, 2015. Emerging infectious diseases, 25(7), 1281–1288.spa
dc.rights.coarhttp://purl.org/coar/access_right/c_abf2spa
dc.rights.licenseAtribución-NoComercial-SinDerivadas 2.5 Colombia*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/2.5/co/*
dc.subjectResistenciaspa
dc.subjectAntibióticosspa
dc.subjectMecanismosspa
dc.subjectGrupo E-ESKAPEspa
dc.subjectGram negativasspa
dc.subjectGram positivasspa
dc.subjectInfecciones intrahospitalariasspa
dc.subjectSuelospa
dc.subjectAguasspa
dc.subjectAnimalesspa
dc.subjectEnterococcus faecalisspa
dc.subjectEpidemiologíaspa
dc.subjectInfecciones asociadas a la atención en saludspa
dc.subjectStaphylococcus aureus resistente a meticilinaspa
dc.subjectmecAspa
dc.subjectEstudiantesspa
dc.subjectPatrones de resistenciaspa
dc.subjectVariabilidad genéticaspa
dc.subject.lembResistencia a los medicamentos en microorganismosspa
dc.subject.lembMicroorganismos - Efecto de los medicamentosspa
dc.subject.lembMicroorganismos patógenosspa
dc.subject.lembMicrobiología médica I. Cerón Marín, Valentina, autora II. Chávez Vivas, Mónica, autora III. Gómez Naranjo, Rommel Fabián, autor IV. Quintero Cundumí, Sandra Lorena, autora V. Vargas Gutiérrez, Valentina, autoraspa
dc.subject.subjectenglishResistancespa
dc.subject.subjectenglishAntibioticsspa
dc.subject.subjectenglishMechanismsspa
dc.subject.subjectenglishE-ESKAPE groupspa
dc.subject.subjectenglishGram negativespa
dc.subject.subjectenglishGram positivespa
dc.subject.subjectenglishIntrahopsitary infectionsspa
dc.subject.subjectenglishSoilspa
dc.subject.subjectenglishWaterspa
dc.subject.subjectenglishAnimalsspa
dc.subject.subjectenglishEnterococcus faecalisspa
dc.subject.subjectenglishEpidemiologyspa
dc.subject.subjectenglishInfections associated with health carespa
dc.subject.subjectenglishMethicillin-resistant Staphylococcus aureusspa
dc.subject.subjectenglishmecAspa
dc.subject.subjectenglishStudentsspa
dc.subject.subjectenglishPseudomonas aeruginosaspa
dc.subject.subjectenglishPseudomonas aeruginosaspa
dc.subject.subjectenglishResistance patternsspa
dc.subject.subjectenglishGenetic variabilityspa
dc.titleDesafíos para enfrentar la resistencia a los antibióticos en bacterias patógenas en el tercer decenio del siglo XXIspa

Archivos

Bloque original

Mostrando 1 - 2 de 2
Cargando...
Miniatura
Nombre:
Desafíos para enfrentar la resistencia a los antibióticos en bacteria patógenas en el tercer decenio del siglo XXI.pdf
Tamaño:
3.69 MB
Formato:
Adobe Portable Document Format
Descripción:
Cargando...
Miniatura
Nombre:
Formato de Cesión de Derechos.pdf
Tamaño:
274.95 KB
Formato:
Adobe Portable Document Format
Descripción:

Bloque de licencias

Mostrando 1 - 1 de 1
Cargando...
Miniatura
Nombre:
license.txt
Tamaño:
1.71 KB
Formato:
Item-specific license agreed upon to submission
Descripción: