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Gut microbiota from high-risk men who have sex with men drive immune activation in gnotobiotic mice and in vitro HIV infection

Men who have sex with men (MSM) have differences in immune activation and gut microbiome composition compared with men who have sex with women (MSW), even in the absence of HIV infection. Gut microbiome differences associated with HIV itself when controlling for MSM, as assessed by 16S rRNA sequenci...

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Autores principales: Li, Sam X., Sen, Sharon, Schneider, Jennifer M., Xiong, Ka-Na, Nusbacher, Nichole M., Moreno-Huizar, Nancy, Shaffer, Michael, Armstrong, Abigail J. S., Severs, Erin, Kuhn, Kristine, Neff, Charles P., McCarter, Martin, Campbell, Thomas, Lozupone, Catherine A., Palmer, Brent E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6448819/
https://www.ncbi.nlm.nih.gov/pubmed/30947289
http://dx.doi.org/10.1371/journal.ppat.1007611
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author Li, Sam X.
Sen, Sharon
Schneider, Jennifer M.
Xiong, Ka-Na
Nusbacher, Nichole M.
Moreno-Huizar, Nancy
Shaffer, Michael
Armstrong, Abigail J. S.
Severs, Erin
Kuhn, Kristine
Neff, Charles P.
McCarter, Martin
Campbell, Thomas
Lozupone, Catherine A.
Palmer, Brent E.
author_facet Li, Sam X.
Sen, Sharon
Schneider, Jennifer M.
Xiong, Ka-Na
Nusbacher, Nichole M.
Moreno-Huizar, Nancy
Shaffer, Michael
Armstrong, Abigail J. S.
Severs, Erin
Kuhn, Kristine
Neff, Charles P.
McCarter, Martin
Campbell, Thomas
Lozupone, Catherine A.
Palmer, Brent E.
author_sort Li, Sam X.
collection PubMed
description Men who have sex with men (MSM) have differences in immune activation and gut microbiome composition compared with men who have sex with women (MSW), even in the absence of HIV infection. Gut microbiome differences associated with HIV itself when controlling for MSM, as assessed by 16S rRNA sequencing, are relatively subtle. Understanding whether gut microbiome composition impacts immune activation in HIV-negative and HIV-positive MSM has important implications since immune activation has been associated with HIV acquisition risk and disease progression. To investigate the effects of MSM and HIV-associated gut microbiota on immune activation, we transplanted feces from HIV-negative MSW, HIV-negative MSM, and HIV-positive untreated MSM to gnotobiotic mice. Following transplant, 16S rRNA gene sequencing determined that the microbiomes of MSM and MSW maintained distinct compositions in mice and that specific microbial differences between MSM and MSW were replicated. Immunologically, HIV-negative MSM donors had higher frequencies of blood CD38+ HLADR+ and CD103+ T cells and their fecal recipients had higher frequencies of gut CD69+ and CD103+ T cells, compared with HIV-negative MSW donors and recipients, respectively. Significant microbiome differences were not detected between HIV-negative and HIV-positive MSM in this small donor cohort, and immune differences between their recipients were trending but not statistically significant. A larger donor cohort may therefore be needed to detect immune-modulating microbes associated with HIV. To investigate whether our findings in mice could have implications for HIV replication, we infected primary human lamina propria cells stimulated with isolated fecal microbiota, and found that microbiota from MSM stimulated higher frequencies of HIV-infected cells than microbiota from MSW. Finally, we identified several microbes that correlated with immune readouts in both fecal recipients and donors, and with in vitro HIV infection, which suggests a role for gut microbiota in immune activation and potentially HIV acquisition in MSM.
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spelling pubmed-64488192019-04-19 Gut microbiota from high-risk men who have sex with men drive immune activation in gnotobiotic mice and in vitro HIV infection Li, Sam X. Sen, Sharon Schneider, Jennifer M. Xiong, Ka-Na Nusbacher, Nichole M. Moreno-Huizar, Nancy Shaffer, Michael Armstrong, Abigail J. S. Severs, Erin Kuhn, Kristine Neff, Charles P. McCarter, Martin Campbell, Thomas Lozupone, Catherine A. Palmer, Brent E. PLoS Pathog Research Article Men who have sex with men (MSM) have differences in immune activation and gut microbiome composition compared with men who have sex with women (MSW), even in the absence of HIV infection. Gut microbiome differences associated with HIV itself when controlling for MSM, as assessed by 16S rRNA sequencing, are relatively subtle. Understanding whether gut microbiome composition impacts immune activation in HIV-negative and HIV-positive MSM has important implications since immune activation has been associated with HIV acquisition risk and disease progression. To investigate the effects of MSM and HIV-associated gut microbiota on immune activation, we transplanted feces from HIV-negative MSW, HIV-negative MSM, and HIV-positive untreated MSM to gnotobiotic mice. Following transplant, 16S rRNA gene sequencing determined that the microbiomes of MSM and MSW maintained distinct compositions in mice and that specific microbial differences between MSM and MSW were replicated. Immunologically, HIV-negative MSM donors had higher frequencies of blood CD38+ HLADR+ and CD103+ T cells and their fecal recipients had higher frequencies of gut CD69+ and CD103+ T cells, compared with HIV-negative MSW donors and recipients, respectively. Significant microbiome differences were not detected between HIV-negative and HIV-positive MSM in this small donor cohort, and immune differences between their recipients were trending but not statistically significant. A larger donor cohort may therefore be needed to detect immune-modulating microbes associated with HIV. To investigate whether our findings in mice could have implications for HIV replication, we infected primary human lamina propria cells stimulated with isolated fecal microbiota, and found that microbiota from MSM stimulated higher frequencies of HIV-infected cells than microbiota from MSW. Finally, we identified several microbes that correlated with immune readouts in both fecal recipients and donors, and with in vitro HIV infection, which suggests a role for gut microbiota in immune activation and potentially HIV acquisition in MSM. Public Library of Science 2019-04-04 /pmc/articles/PMC6448819/ /pubmed/30947289 http://dx.doi.org/10.1371/journal.ppat.1007611 Text en © 2019 Li 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
Li, Sam X.
Sen, Sharon
Schneider, Jennifer M.
Xiong, Ka-Na
Nusbacher, Nichole M.
Moreno-Huizar, Nancy
Shaffer, Michael
Armstrong, Abigail J. S.
Severs, Erin
Kuhn, Kristine
Neff, Charles P.
McCarter, Martin
Campbell, Thomas
Lozupone, Catherine A.
Palmer, Brent E.
Gut microbiota from high-risk men who have sex with men drive immune activation in gnotobiotic mice and in vitro HIV infection
title Gut microbiota from high-risk men who have sex with men drive immune activation in gnotobiotic mice and in vitro HIV infection
title_full Gut microbiota from high-risk men who have sex with men drive immune activation in gnotobiotic mice and in vitro HIV infection
title_fullStr Gut microbiota from high-risk men who have sex with men drive immune activation in gnotobiotic mice and in vitro HIV infection
title_full_unstemmed Gut microbiota from high-risk men who have sex with men drive immune activation in gnotobiotic mice and in vitro HIV infection
title_short Gut microbiota from high-risk men who have sex with men drive immune activation in gnotobiotic mice and in vitro HIV infection
title_sort gut microbiota from high-risk men who have sex with men drive immune activation in gnotobiotic mice and in vitro hiv infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6448819/
https://www.ncbi.nlm.nih.gov/pubmed/30947289
http://dx.doi.org/10.1371/journal.ppat.1007611
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