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Interconnected microbiomes and resistomes in low-income human habitats

Antibiotic-resistant infections annually claim hundreds of thousands of lives worldwide. This problem is exacerbated by resistance gene exchange between pathogens and benign microbes from diverse habitats. Mapping resistance gene dissemination between humans and their environment is a public health...

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Autores principales: Pehrsson, Erica C., Tsukayama, Pablo, Patel, Sanket, Mejía-Bautista, Melissa, Sosa-Soto, Giordano, Navarrete, Karla M., Calderon, Maritza, Cabrera, Lilia, Hoyos-Arango, William, Bertoli, M. Teresita, Berg, Douglas E., Gilman, Robert H., Dantas, Gautam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4869995/
https://www.ncbi.nlm.nih.gov/pubmed/27172044
http://dx.doi.org/10.1038/nature17672
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author Pehrsson, Erica C.
Tsukayama, Pablo
Patel, Sanket
Mejía-Bautista, Melissa
Sosa-Soto, Giordano
Navarrete, Karla M.
Calderon, Maritza
Cabrera, Lilia
Hoyos-Arango, William
Bertoli, M. Teresita
Berg, Douglas E.
Gilman, Robert H.
Dantas, Gautam
author_facet Pehrsson, Erica C.
Tsukayama, Pablo
Patel, Sanket
Mejía-Bautista, Melissa
Sosa-Soto, Giordano
Navarrete, Karla M.
Calderon, Maritza
Cabrera, Lilia
Hoyos-Arango, William
Bertoli, M. Teresita
Berg, Douglas E.
Gilman, Robert H.
Dantas, Gautam
author_sort Pehrsson, Erica C.
collection PubMed
description Antibiotic-resistant infections annually claim hundreds of thousands of lives worldwide. This problem is exacerbated by resistance gene exchange between pathogens and benign microbes from diverse habitats. Mapping resistance gene dissemination between humans and their environment is a public health priority. We characterized the bacterial community structure and resistance exchange networks of hundreds of interconnected human fecal and environmental samples from two low-income Latin American communities. We found that resistomes across habitats are generally structured by bacterial phylogeny along ecological gradients, but identified key resistance genes that cross habitat boundaries and determined their association with mobile genetic elements. We also assessed the effectiveness of widely-used excreta management strategies in reducing fecal bacteria and resistance genes in these settings representative of low- and middle-income countries. Our results lay the foundation for quantitative risk assessment and surveillance of resistance dissemination across interconnected habitats in settings representing over two-thirds of the world’s population.
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spelling pubmed-48699952016-11-11 Interconnected microbiomes and resistomes in low-income human habitats Pehrsson, Erica C. Tsukayama, Pablo Patel, Sanket Mejía-Bautista, Melissa Sosa-Soto, Giordano Navarrete, Karla M. Calderon, Maritza Cabrera, Lilia Hoyos-Arango, William Bertoli, M. Teresita Berg, Douglas E. Gilman, Robert H. Dantas, Gautam Nature Article Antibiotic-resistant infections annually claim hundreds of thousands of lives worldwide. This problem is exacerbated by resistance gene exchange between pathogens and benign microbes from diverse habitats. Mapping resistance gene dissemination between humans and their environment is a public health priority. We characterized the bacterial community structure and resistance exchange networks of hundreds of interconnected human fecal and environmental samples from two low-income Latin American communities. We found that resistomes across habitats are generally structured by bacterial phylogeny along ecological gradients, but identified key resistance genes that cross habitat boundaries and determined their association with mobile genetic elements. We also assessed the effectiveness of widely-used excreta management strategies in reducing fecal bacteria and resistance genes in these settings representative of low- and middle-income countries. Our results lay the foundation for quantitative risk assessment and surveillance of resistance dissemination across interconnected habitats in settings representing over two-thirds of the world’s population. 2016-05-11 /pmc/articles/PMC4869995/ /pubmed/27172044 http://dx.doi.org/10.1038/nature17672 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms Reprints and permissions information is available at www.nature.com/reprints.
spellingShingle Article
Pehrsson, Erica C.
Tsukayama, Pablo
Patel, Sanket
Mejía-Bautista, Melissa
Sosa-Soto, Giordano
Navarrete, Karla M.
Calderon, Maritza
Cabrera, Lilia
Hoyos-Arango, William
Bertoli, M. Teresita
Berg, Douglas E.
Gilman, Robert H.
Dantas, Gautam
Interconnected microbiomes and resistomes in low-income human habitats
title Interconnected microbiomes and resistomes in low-income human habitats
title_full Interconnected microbiomes and resistomes in low-income human habitats
title_fullStr Interconnected microbiomes and resistomes in low-income human habitats
title_full_unstemmed Interconnected microbiomes and resistomes in low-income human habitats
title_short Interconnected microbiomes and resistomes in low-income human habitats
title_sort interconnected microbiomes and resistomes in low-income human habitats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4869995/
https://www.ncbi.nlm.nih.gov/pubmed/27172044
http://dx.doi.org/10.1038/nature17672
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