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Chemostat culture systems support diverse bacteriophage communities from human feces

BACKGROUND: Most human microbiota studies focus on bacteria inhabiting body surfaces, but these surfaces also are home to large populations of viruses. Many are bacteriophages, and their role in driving bacterial diversity is difficult to decipher without the use of in vitro ecosystems that can repr...

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Autores principales: Santiago-Rodriguez, Tasha M., Ly, Melissa, Daigneault, Michelle C., Brown, Ian H. L., McDonald, Julie A. K., Bonilla, Natasha, Vercoe, Emma Allen, Pride, David T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4638026/
https://www.ncbi.nlm.nih.gov/pubmed/26549756
http://dx.doi.org/10.1186/s40168-015-0124-3
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author Santiago-Rodriguez, Tasha M.
Ly, Melissa
Daigneault, Michelle C.
Brown, Ian H. L.
McDonald, Julie A. K.
Bonilla, Natasha
Vercoe, Emma Allen
Pride, David T.
author_facet Santiago-Rodriguez, Tasha M.
Ly, Melissa
Daigneault, Michelle C.
Brown, Ian H. L.
McDonald, Julie A. K.
Bonilla, Natasha
Vercoe, Emma Allen
Pride, David T.
author_sort Santiago-Rodriguez, Tasha M.
collection PubMed
description BACKGROUND: Most human microbiota studies focus on bacteria inhabiting body surfaces, but these surfaces also are home to large populations of viruses. Many are bacteriophages, and their role in driving bacterial diversity is difficult to decipher without the use of in vitro ecosystems that can reproduce human microbial communities. RESULTS: We used chemostat culture systems known to harbor diverse fecal bacteria to decipher whether these cultures also are home to phage communities. We found that there are vast viral communities inhabiting these ecosystems, with estimated concentrations similar to those found in human feces. The viral communities are composed entirely of bacteriophages and likely contain both temperate and lytic phages based on their similarities to other known phages. We examined the cultured phage communities at five separate time points over 24 days and found that they were highly individual-specific, suggesting that much of the subject-specificity found in human viromes also is captured by this culture-based system. A high proportion of the community membership is conserved over time, but the cultured communities maintain more similarity with other intra-subject cultures than they do to human feces. In four of the five subjects, estimated viral diversity between fecal and cultured communities was highly similar. CONCLUSIONS: Because the diversity of phages in these cultured fecal communities have similarities to those found in humans, we believe these communities can serve as valuable ecosystems to help uncover the role of phages in human microbial communities. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40168-015-0124-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-46380262015-11-10 Chemostat culture systems support diverse bacteriophage communities from human feces Santiago-Rodriguez, Tasha M. Ly, Melissa Daigneault, Michelle C. Brown, Ian H. L. McDonald, Julie A. K. Bonilla, Natasha Vercoe, Emma Allen Pride, David T. Microbiome Research BACKGROUND: Most human microbiota studies focus on bacteria inhabiting body surfaces, but these surfaces also are home to large populations of viruses. Many are bacteriophages, and their role in driving bacterial diversity is difficult to decipher without the use of in vitro ecosystems that can reproduce human microbial communities. RESULTS: We used chemostat culture systems known to harbor diverse fecal bacteria to decipher whether these cultures also are home to phage communities. We found that there are vast viral communities inhabiting these ecosystems, with estimated concentrations similar to those found in human feces. The viral communities are composed entirely of bacteriophages and likely contain both temperate and lytic phages based on their similarities to other known phages. We examined the cultured phage communities at five separate time points over 24 days and found that they were highly individual-specific, suggesting that much of the subject-specificity found in human viromes also is captured by this culture-based system. A high proportion of the community membership is conserved over time, but the cultured communities maintain more similarity with other intra-subject cultures than they do to human feces. In four of the five subjects, estimated viral diversity between fecal and cultured communities was highly similar. CONCLUSIONS: Because the diversity of phages in these cultured fecal communities have similarities to those found in humans, we believe these communities can serve as valuable ecosystems to help uncover the role of phages in human microbial communities. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40168-015-0124-3) contains supplementary material, which is available to authorized users. BioMed Central 2015-11-09 /pmc/articles/PMC4638026/ /pubmed/26549756 http://dx.doi.org/10.1186/s40168-015-0124-3 Text en © Santiago-Rodriguez et al. 2015 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
Santiago-Rodriguez, Tasha M.
Ly, Melissa
Daigneault, Michelle C.
Brown, Ian H. L.
McDonald, Julie A. K.
Bonilla, Natasha
Vercoe, Emma Allen
Pride, David T.
Chemostat culture systems support diverse bacteriophage communities from human feces
title Chemostat culture systems support diverse bacteriophage communities from human feces
title_full Chemostat culture systems support diverse bacteriophage communities from human feces
title_fullStr Chemostat culture systems support diverse bacteriophage communities from human feces
title_full_unstemmed Chemostat culture systems support diverse bacteriophage communities from human feces
title_short Chemostat culture systems support diverse bacteriophage communities from human feces
title_sort chemostat culture systems support diverse bacteriophage communities from human feces
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4638026/
https://www.ncbi.nlm.nih.gov/pubmed/26549756
http://dx.doi.org/10.1186/s40168-015-0124-3
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