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Detection of critical antibiotic resistance genes through routine microbiome surveillance

Population-based public health data on antibiotic resistance gene carriage is poorly surveyed. Research of the human microbiome as an antibiotic resistance reservoir has primarily focused on gut associated microbial communities, but data have shown more widespread microbial colonization across organ...

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Detalles Bibliográficos
Autores principales: Burcham, Zachary M., Schmidt, Carl J., Pechal, Jennifer L., Brooks, Christopher P., Rosch, Jason W., Benbow, M. Eric, Jordan, Heather R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6417727/
https://www.ncbi.nlm.nih.gov/pubmed/30870464
http://dx.doi.org/10.1371/journal.pone.0213280
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author Burcham, Zachary M.
Schmidt, Carl J.
Pechal, Jennifer L.
Brooks, Christopher P.
Rosch, Jason W.
Benbow, M. Eric
Jordan, Heather R.
author_facet Burcham, Zachary M.
Schmidt, Carl J.
Pechal, Jennifer L.
Brooks, Christopher P.
Rosch, Jason W.
Benbow, M. Eric
Jordan, Heather R.
author_sort Burcham, Zachary M.
collection PubMed
description Population-based public health data on antibiotic resistance gene carriage is poorly surveyed. Research of the human microbiome as an antibiotic resistance reservoir has primarily focused on gut associated microbial communities, but data have shown more widespread microbial colonization across organs than originally believed, with organs previously considered as sterile being colonized. Our study demonstrates the utility of postmortem microbiome sampling during routine autopsy as a method to survey antibiotic resistance carriage in a general population. Postmortem microbial sampling detected pathogens of public health concern including genes for multidrug efflux pumps, carbapenem, methicillin, vancomycin, and polymixin resistances. Results suggest that postmortem assessments of host-associated microbial communities are useful in acquiring community specific data while reducing selective-participant biases.
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spelling pubmed-64177272019-04-01 Detection of critical antibiotic resistance genes through routine microbiome surveillance Burcham, Zachary M. Schmidt, Carl J. Pechal, Jennifer L. Brooks, Christopher P. Rosch, Jason W. Benbow, M. Eric Jordan, Heather R. PLoS One Research Article Population-based public health data on antibiotic resistance gene carriage is poorly surveyed. Research of the human microbiome as an antibiotic resistance reservoir has primarily focused on gut associated microbial communities, but data have shown more widespread microbial colonization across organs than originally believed, with organs previously considered as sterile being colonized. Our study demonstrates the utility of postmortem microbiome sampling during routine autopsy as a method to survey antibiotic resistance carriage in a general population. Postmortem microbial sampling detected pathogens of public health concern including genes for multidrug efflux pumps, carbapenem, methicillin, vancomycin, and polymixin resistances. Results suggest that postmortem assessments of host-associated microbial communities are useful in acquiring community specific data while reducing selective-participant biases. Public Library of Science 2019-03-14 /pmc/articles/PMC6417727/ /pubmed/30870464 http://dx.doi.org/10.1371/journal.pone.0213280 Text en © 2019 Burcham et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Burcham, Zachary M.
Schmidt, Carl J.
Pechal, Jennifer L.
Brooks, Christopher P.
Rosch, Jason W.
Benbow, M. Eric
Jordan, Heather R.
Detection of critical antibiotic resistance genes through routine microbiome surveillance
title Detection of critical antibiotic resistance genes through routine microbiome surveillance
title_full Detection of critical antibiotic resistance genes through routine microbiome surveillance
title_fullStr Detection of critical antibiotic resistance genes through routine microbiome surveillance
title_full_unstemmed Detection of critical antibiotic resistance genes through routine microbiome surveillance
title_short Detection of critical antibiotic resistance genes through routine microbiome surveillance
title_sort detection of critical antibiotic resistance genes through routine microbiome surveillance
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6417727/
https://www.ncbi.nlm.nih.gov/pubmed/30870464
http://dx.doi.org/10.1371/journal.pone.0213280
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