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Meta-transcriptomics reveals a diverse antibiotic resistance gene pool in avian microbiomes

BACKGROUND: Antibiotic resistance is rendering common bacterial infections untreatable. Wildlife can incorporate and disperse antibiotic-resistant bacteria in the environment, such as water systems, which in turn serve as reservoirs of resistance genes for human pathogens. Anthropogenic activity may...

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Autores principales: Marcelino, Vanessa R., Wille, Michelle, Hurt, Aeron C., González-Acuña, Daniel, Klaassen, Marcel, Schlub, Timothy E., Eden, John-Sebastian, Shi, Mang, Iredell, Jonathan R., Sorrell, Tania C., Holmes, Edward C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6454771/
https://www.ncbi.nlm.nih.gov/pubmed/30961590
http://dx.doi.org/10.1186/s12915-019-0649-1
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author Marcelino, Vanessa R.
Wille, Michelle
Hurt, Aeron C.
González-Acuña, Daniel
Klaassen, Marcel
Schlub, Timothy E.
Eden, John-Sebastian
Shi, Mang
Iredell, Jonathan R.
Sorrell, Tania C.
Holmes, Edward C.
author_facet Marcelino, Vanessa R.
Wille, Michelle
Hurt, Aeron C.
González-Acuña, Daniel
Klaassen, Marcel
Schlub, Timothy E.
Eden, John-Sebastian
Shi, Mang
Iredell, Jonathan R.
Sorrell, Tania C.
Holmes, Edward C.
author_sort Marcelino, Vanessa R.
collection PubMed
description BACKGROUND: Antibiotic resistance is rendering common bacterial infections untreatable. Wildlife can incorporate and disperse antibiotic-resistant bacteria in the environment, such as water systems, which in turn serve as reservoirs of resistance genes for human pathogens. Anthropogenic activity may contribute to the spread of bacterial resistance cycling through natural environments, including through the release of human waste, as sewage treatment only partially removes antibiotic-resistant bacteria. However, empirical data supporting these effects are currently limited. Here we used bulk RNA-sequencing (meta-transcriptomics) to assess the diversity and expression levels of functionally viable resistance genes in the gut microbiome of birds with aquatic habits in diverse locations. RESULTS: We found antibiotic resistance genes in birds from all localities, from penguins in Antarctica to ducks in a wastewater treatment plant in Australia. Comparative analysis revealed that birds feeding at the wastewater treatment plant carried the greatest resistance gene burden, including genes typically associated with multidrug resistance plasmids as the aac(6)-Ib-cr gene. Differences in resistance gene burden also reflected aspects of bird ecology, taxonomy, and microbial function. Notably, ducks, which feed by dabbling, carried a higher abundance and diversity of resistance genes than turnstones, avocets, and penguins, which usually prey on more pristine waters. CONCLUSIONS: These transcriptome data suggest that human waste, even if it undergoes treatment, might contribute to the spread of antibiotic resistance genes to the wild. Differences in microbiome functioning across different bird lineages may also play a role in the antibiotic resistance burden carried by wild birds. In summary, we reveal the complex factors explaining the distribution of resistance genes and their exchange routes between humans and wildlife, and show that meta-transcriptomics is a valuable tool to access functional resistance genes in whole microbial communities. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12915-019-0649-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-64547712019-04-19 Meta-transcriptomics reveals a diverse antibiotic resistance gene pool in avian microbiomes Marcelino, Vanessa R. Wille, Michelle Hurt, Aeron C. González-Acuña, Daniel Klaassen, Marcel Schlub, Timothy E. Eden, John-Sebastian Shi, Mang Iredell, Jonathan R. Sorrell, Tania C. Holmes, Edward C. BMC Biol Research Article BACKGROUND: Antibiotic resistance is rendering common bacterial infections untreatable. Wildlife can incorporate and disperse antibiotic-resistant bacteria in the environment, such as water systems, which in turn serve as reservoirs of resistance genes for human pathogens. Anthropogenic activity may contribute to the spread of bacterial resistance cycling through natural environments, including through the release of human waste, as sewage treatment only partially removes antibiotic-resistant bacteria. However, empirical data supporting these effects are currently limited. Here we used bulk RNA-sequencing (meta-transcriptomics) to assess the diversity and expression levels of functionally viable resistance genes in the gut microbiome of birds with aquatic habits in diverse locations. RESULTS: We found antibiotic resistance genes in birds from all localities, from penguins in Antarctica to ducks in a wastewater treatment plant in Australia. Comparative analysis revealed that birds feeding at the wastewater treatment plant carried the greatest resistance gene burden, including genes typically associated with multidrug resistance plasmids as the aac(6)-Ib-cr gene. Differences in resistance gene burden also reflected aspects of bird ecology, taxonomy, and microbial function. Notably, ducks, which feed by dabbling, carried a higher abundance and diversity of resistance genes than turnstones, avocets, and penguins, which usually prey on more pristine waters. CONCLUSIONS: These transcriptome data suggest that human waste, even if it undergoes treatment, might contribute to the spread of antibiotic resistance genes to the wild. Differences in microbiome functioning across different bird lineages may also play a role in the antibiotic resistance burden carried by wild birds. In summary, we reveal the complex factors explaining the distribution of resistance genes and their exchange routes between humans and wildlife, and show that meta-transcriptomics is a valuable tool to access functional resistance genes in whole microbial communities. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12915-019-0649-1) contains supplementary material, which is available to authorized users. BioMed Central 2019-04-08 /pmc/articles/PMC6454771/ /pubmed/30961590 http://dx.doi.org/10.1186/s12915-019-0649-1 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Marcelino, Vanessa R.
Wille, Michelle
Hurt, Aeron C.
González-Acuña, Daniel
Klaassen, Marcel
Schlub, Timothy E.
Eden, John-Sebastian
Shi, Mang
Iredell, Jonathan R.
Sorrell, Tania C.
Holmes, Edward C.
Meta-transcriptomics reveals a diverse antibiotic resistance gene pool in avian microbiomes
title Meta-transcriptomics reveals a diverse antibiotic resistance gene pool in avian microbiomes
title_full Meta-transcriptomics reveals a diverse antibiotic resistance gene pool in avian microbiomes
title_fullStr Meta-transcriptomics reveals a diverse antibiotic resistance gene pool in avian microbiomes
title_full_unstemmed Meta-transcriptomics reveals a diverse antibiotic resistance gene pool in avian microbiomes
title_short Meta-transcriptomics reveals a diverse antibiotic resistance gene pool in avian microbiomes
title_sort meta-transcriptomics reveals a diverse antibiotic resistance gene pool in avian microbiomes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6454771/
https://www.ncbi.nlm.nih.gov/pubmed/30961590
http://dx.doi.org/10.1186/s12915-019-0649-1
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