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Effects of Long Term Antibiotic Therapy on Human Oral and Fecal Viromes

Viruses are integral members of the human microbiome. Many of the viruses comprising the human virome have been identified as bacteriophage, and little is known about how they respond to perturbations within the human ecosystem. The intimate association of phage with their cellular hosts suggests th...

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Autores principales: Abeles, Shira R., Ly, Melissa, Santiago-Rodriguez, Tasha M., Pride, David T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4550281/
https://www.ncbi.nlm.nih.gov/pubmed/26309137
http://dx.doi.org/10.1371/journal.pone.0134941
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author Abeles, Shira R.
Ly, Melissa
Santiago-Rodriguez, Tasha M.
Pride, David T.
author_facet Abeles, Shira R.
Ly, Melissa
Santiago-Rodriguez, Tasha M.
Pride, David T.
author_sort Abeles, Shira R.
collection PubMed
description Viruses are integral members of the human microbiome. Many of the viruses comprising the human virome have been identified as bacteriophage, and little is known about how they respond to perturbations within the human ecosystem. The intimate association of phage with their cellular hosts suggests their communities may change in response to shifts in bacterial community membership. Alterations to human bacterial biota can result in human disease including a reduction in the host's resilience to pathogens. Here we report the ecology of oral and fecal viral communities and their responses to long-term antibiotic therapy in a cohort of human subjects. We found significant differences between the viral communities of each body site with a more heterogeneous fecal virus community compared with viruses in saliva. We measured the relative diversity of viruses, and found that the oral viromes were significantly more diverse than fecal viromes. There were characteristic changes in the membership of oral and fecal bacterial communities in response to antibiotics, but changes in fecal viral communities were less distinguishing. In the oral cavity, an abundance of papillomaviruses found in subjects on antibiotics suggests an association between antibiotics and papillomavirus production. Despite the abundance of papillomaviruses identified, in neither the oral nor the fecal viromes did antibiotic therapy have any significant impact upon overall viral diversity. There was, however, an apparent expansion of the reservoir of genes putatively involved in resistance to numerous classes of antibiotics in fecal viromes that was not paralleled in oral viromes. The emergence of antibiotic resistance in fecal viromes in response to long-term antibiotic therapy in humans suggests that viruses play an important role in the resilience of human microbial communities to antibiotic disturbances.
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spelling pubmed-45502812015-09-01 Effects of Long Term Antibiotic Therapy on Human Oral and Fecal Viromes Abeles, Shira R. Ly, Melissa Santiago-Rodriguez, Tasha M. Pride, David T. PLoS One Research Article Viruses are integral members of the human microbiome. Many of the viruses comprising the human virome have been identified as bacteriophage, and little is known about how they respond to perturbations within the human ecosystem. The intimate association of phage with their cellular hosts suggests their communities may change in response to shifts in bacterial community membership. Alterations to human bacterial biota can result in human disease including a reduction in the host's resilience to pathogens. Here we report the ecology of oral and fecal viral communities and their responses to long-term antibiotic therapy in a cohort of human subjects. We found significant differences between the viral communities of each body site with a more heterogeneous fecal virus community compared with viruses in saliva. We measured the relative diversity of viruses, and found that the oral viromes were significantly more diverse than fecal viromes. There were characteristic changes in the membership of oral and fecal bacterial communities in response to antibiotics, but changes in fecal viral communities were less distinguishing. In the oral cavity, an abundance of papillomaviruses found in subjects on antibiotics suggests an association between antibiotics and papillomavirus production. Despite the abundance of papillomaviruses identified, in neither the oral nor the fecal viromes did antibiotic therapy have any significant impact upon overall viral diversity. There was, however, an apparent expansion of the reservoir of genes putatively involved in resistance to numerous classes of antibiotics in fecal viromes that was not paralleled in oral viromes. The emergence of antibiotic resistance in fecal viromes in response to long-term antibiotic therapy in humans suggests that viruses play an important role in the resilience of human microbial communities to antibiotic disturbances. Public Library of Science 2015-08-26 /pmc/articles/PMC4550281/ /pubmed/26309137 http://dx.doi.org/10.1371/journal.pone.0134941 Text en © 2015 Abeles 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Abeles, Shira R.
Ly, Melissa
Santiago-Rodriguez, Tasha M.
Pride, David T.
Effects of Long Term Antibiotic Therapy on Human Oral and Fecal Viromes
title Effects of Long Term Antibiotic Therapy on Human Oral and Fecal Viromes
title_full Effects of Long Term Antibiotic Therapy on Human Oral and Fecal Viromes
title_fullStr Effects of Long Term Antibiotic Therapy on Human Oral and Fecal Viromes
title_full_unstemmed Effects of Long Term Antibiotic Therapy on Human Oral and Fecal Viromes
title_short Effects of Long Term Antibiotic Therapy on Human Oral and Fecal Viromes
title_sort effects of long term antibiotic therapy on human oral and fecal viromes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4550281/
https://www.ncbi.nlm.nih.gov/pubmed/26309137
http://dx.doi.org/10.1371/journal.pone.0134941
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