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Genomic characterization of multidrug‐resistant ESBL‐producing Escherichia coli ST58 causing fatal colibacillosis in critically endangered Brazilian merganser (Mergus octosetaceus)

Even though antimicrobial‐resistant bacteria have begun to be detected in wildlife, raising important issues related to their transmission and persistence of clinically important pathogens in the environment, little is known about the role of these bacteria on wildlife health, especially on endanger...

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Autores principales: Fuentes‐Castillo, Danny, Navas‐Suárez, Pedro Enrique, Gondim, Maria Fernanda, Esposito, Fernanda, Sacristán, Carlos, Fontana, Herrison, Fuga, Bruna, Piovani, Camila, Kooij, Robert, Lincopan, Nilton, Catão‐Dias, José Luiz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8246901/
https://www.ncbi.nlm.nih.gov/pubmed/32544292
http://dx.doi.org/10.1111/tbed.13686
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author Fuentes‐Castillo, Danny
Navas‐Suárez, Pedro Enrique
Gondim, Maria Fernanda
Esposito, Fernanda
Sacristán, Carlos
Fontana, Herrison
Fuga, Bruna
Piovani, Camila
Kooij, Robert
Lincopan, Nilton
Catão‐Dias, José Luiz
author_facet Fuentes‐Castillo, Danny
Navas‐Suárez, Pedro Enrique
Gondim, Maria Fernanda
Esposito, Fernanda
Sacristán, Carlos
Fontana, Herrison
Fuga, Bruna
Piovani, Camila
Kooij, Robert
Lincopan, Nilton
Catão‐Dias, José Luiz
author_sort Fuentes‐Castillo, Danny
collection PubMed
description Even though antimicrobial‐resistant bacteria have begun to be detected in wildlife, raising important issues related to their transmission and persistence of clinically important pathogens in the environment, little is known about the role of these bacteria on wildlife health, especially on endangered species. The Brazilian merganser (Mergus octosetaceus) is one of the most threatened waterfowl in the world, classified as Critically Endangered by the International Union for Conservation of Nature. In 2019, a fatal case of sepsis was diagnosed in an 8‐day‐old Brazilian merganser inhabiting a zoological park. At necropsy, major gross lesions were pulmonary and hepatic congestion. Using microbiologic and genomic methods, we identified a multidrug‐resistant (MDR) extended‐spectrum β‐lactamase (ESBL) CTX‐M‐8‐producing Escherichia coli (designed as PMPU strain) belonging to the international clone ST58, in coelomic cavity, oesophagus, lungs, small intestine and cloaca samples. PMPU strain harboured a broad resistome against antibiotics (cephalosporins, tetracyclines, aminoglycosides, sulphonamides, trimethoprim and quinolones), domestic/hospital disinfectants and heavy metals (arsenic, mercury, lead, copper and silver). Additionally, the virulence of E. coli PMPU strain was confirmed using a wax moth (Galleria mellonella) infection model, and it was supported by the presence of virulence genes encoding toxins, adherence factors, invasins and iron acquisition systems. Broad resistome and virulome of PMPU contributed to therapeutic failure and death of the animal. In brief, we report for the first time a fatal colibacillosis by MDR ESBL‐producing E. coli in critically endangered Brazilian merganser, highlighting that besides colonization, critical priority pathogens are threatening wildlife. E. coli ST58 clone has been previously reported in humans, food‐producing animals, wildlife and environment, supporting broad adaptation and persistence at human–animal–environment interface.
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spelling pubmed-82469012021-07-02 Genomic characterization of multidrug‐resistant ESBL‐producing Escherichia coli ST58 causing fatal colibacillosis in critically endangered Brazilian merganser (Mergus octosetaceus) Fuentes‐Castillo, Danny Navas‐Suárez, Pedro Enrique Gondim, Maria Fernanda Esposito, Fernanda Sacristán, Carlos Fontana, Herrison Fuga, Bruna Piovani, Camila Kooij, Robert Lincopan, Nilton Catão‐Dias, José Luiz Transbound Emerg Dis Rapid Communications Even though antimicrobial‐resistant bacteria have begun to be detected in wildlife, raising important issues related to their transmission and persistence of clinically important pathogens in the environment, little is known about the role of these bacteria on wildlife health, especially on endangered species. The Brazilian merganser (Mergus octosetaceus) is one of the most threatened waterfowl in the world, classified as Critically Endangered by the International Union for Conservation of Nature. In 2019, a fatal case of sepsis was diagnosed in an 8‐day‐old Brazilian merganser inhabiting a zoological park. At necropsy, major gross lesions were pulmonary and hepatic congestion. Using microbiologic and genomic methods, we identified a multidrug‐resistant (MDR) extended‐spectrum β‐lactamase (ESBL) CTX‐M‐8‐producing Escherichia coli (designed as PMPU strain) belonging to the international clone ST58, in coelomic cavity, oesophagus, lungs, small intestine and cloaca samples. PMPU strain harboured a broad resistome against antibiotics (cephalosporins, tetracyclines, aminoglycosides, sulphonamides, trimethoprim and quinolones), domestic/hospital disinfectants and heavy metals (arsenic, mercury, lead, copper and silver). Additionally, the virulence of E. coli PMPU strain was confirmed using a wax moth (Galleria mellonella) infection model, and it was supported by the presence of virulence genes encoding toxins, adherence factors, invasins and iron acquisition systems. Broad resistome and virulome of PMPU contributed to therapeutic failure and death of the animal. In brief, we report for the first time a fatal colibacillosis by MDR ESBL‐producing E. coli in critically endangered Brazilian merganser, highlighting that besides colonization, critical priority pathogens are threatening wildlife. E. coli ST58 clone has been previously reported in humans, food‐producing animals, wildlife and environment, supporting broad adaptation and persistence at human–animal–environment interface. John Wiley and Sons Inc. 2020-07-02 2021-03 /pmc/articles/PMC8246901/ /pubmed/32544292 http://dx.doi.org/10.1111/tbed.13686 Text en © 2020 The Authors. Transboundary and Emerging Diseases published by Blackwell Verlag GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Rapid Communications
Fuentes‐Castillo, Danny
Navas‐Suárez, Pedro Enrique
Gondim, Maria Fernanda
Esposito, Fernanda
Sacristán, Carlos
Fontana, Herrison
Fuga, Bruna
Piovani, Camila
Kooij, Robert
Lincopan, Nilton
Catão‐Dias, José Luiz
Genomic characterization of multidrug‐resistant ESBL‐producing Escherichia coli ST58 causing fatal colibacillosis in critically endangered Brazilian merganser (Mergus octosetaceus)
title Genomic characterization of multidrug‐resistant ESBL‐producing Escherichia coli ST58 causing fatal colibacillosis in critically endangered Brazilian merganser (Mergus octosetaceus)
title_full Genomic characterization of multidrug‐resistant ESBL‐producing Escherichia coli ST58 causing fatal colibacillosis in critically endangered Brazilian merganser (Mergus octosetaceus)
title_fullStr Genomic characterization of multidrug‐resistant ESBL‐producing Escherichia coli ST58 causing fatal colibacillosis in critically endangered Brazilian merganser (Mergus octosetaceus)
title_full_unstemmed Genomic characterization of multidrug‐resistant ESBL‐producing Escherichia coli ST58 causing fatal colibacillosis in critically endangered Brazilian merganser (Mergus octosetaceus)
title_short Genomic characterization of multidrug‐resistant ESBL‐producing Escherichia coli ST58 causing fatal colibacillosis in critically endangered Brazilian merganser (Mergus octosetaceus)
title_sort genomic characterization of multidrug‐resistant esbl‐producing escherichia coli st58 causing fatal colibacillosis in critically endangered brazilian merganser (mergus octosetaceus)
topic Rapid Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8246901/
https://www.ncbi.nlm.nih.gov/pubmed/32544292
http://dx.doi.org/10.1111/tbed.13686
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