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Gut Bacteria Metabolism Impacts Immune Recovery in HIV-infected Individuals
While changes in gut microbial populations have been described in human immuno-deficiency virus (HIV)-infected patients undergoing antiretroviral therapy (ART), the mechanisms underlying the contributions of gut bacteria and their molecular agents (metabolites and proteins) to immune recovery remain...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4919658/ https://www.ncbi.nlm.nih.gov/pubmed/27428431 http://dx.doi.org/10.1016/j.ebiom.2016.04.033 |
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author | Serrano-Villar, Sergio Rojo, David Martínez-Martínez, Mónica Deusch, Simon Vázquez-Castellanos, Jorge F. Bargiela, Rafael Sainz, Talía Vera, Mar Moreno, Santiago Estrada, Vicente Gosalbes, María José Latorre, Amparo Seifert, Jana Barbas, Coral Moya, Andrés Ferrer, Manuel |
author_facet | Serrano-Villar, Sergio Rojo, David Martínez-Martínez, Mónica Deusch, Simon Vázquez-Castellanos, Jorge F. Bargiela, Rafael Sainz, Talía Vera, Mar Moreno, Santiago Estrada, Vicente Gosalbes, María José Latorre, Amparo Seifert, Jana Barbas, Coral Moya, Andrés Ferrer, Manuel |
author_sort | Serrano-Villar, Sergio |
collection | PubMed |
description | While changes in gut microbial populations have been described in human immuno-deficiency virus (HIV)-infected patients undergoing antiretroviral therapy (ART), the mechanisms underlying the contributions of gut bacteria and their molecular agents (metabolites and proteins) to immune recovery remain unexplored. To study this, we examined the active fraction of the gut microbiome, through examining protein synthesis and accumulation of metabolites inside gut bacteria and in the bloodstream, in 8 healthy controls and 29 HIV-infected individuals (6 being longitudinally studied). We found that HIV infection is associated to dramatic changes in the active set of gut bacteria simultaneously altering the metabolic outcomes. Effects were accentuated among immunological ART responders, regardless diet, subject characteristics, clinical variables other than immune recovery, the duration and type of ART and sexual preferences. The effect was found at quantitative levels of several molecular agents and active bacteria which were herein identified and whose abundance correlated with HIV immune pathogenesis markers. Although, we cannot rule out the possibility that some changes are partially a random consequence of the disease status, our data suggest that most likely reduced inflammation and immune recovery is a joint solution orchestrated by both the active fraction of the gut microbiota and the host. |
format | Online Article Text |
id | pubmed-4919658 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-49196582016-06-30 Gut Bacteria Metabolism Impacts Immune Recovery in HIV-infected Individuals Serrano-Villar, Sergio Rojo, David Martínez-Martínez, Mónica Deusch, Simon Vázquez-Castellanos, Jorge F. Bargiela, Rafael Sainz, Talía Vera, Mar Moreno, Santiago Estrada, Vicente Gosalbes, María José Latorre, Amparo Seifert, Jana Barbas, Coral Moya, Andrés Ferrer, Manuel EBioMedicine Research Paper While changes in gut microbial populations have been described in human immuno-deficiency virus (HIV)-infected patients undergoing antiretroviral therapy (ART), the mechanisms underlying the contributions of gut bacteria and their molecular agents (metabolites and proteins) to immune recovery remain unexplored. To study this, we examined the active fraction of the gut microbiome, through examining protein synthesis and accumulation of metabolites inside gut bacteria and in the bloodstream, in 8 healthy controls and 29 HIV-infected individuals (6 being longitudinally studied). We found that HIV infection is associated to dramatic changes in the active set of gut bacteria simultaneously altering the metabolic outcomes. Effects were accentuated among immunological ART responders, regardless diet, subject characteristics, clinical variables other than immune recovery, the duration and type of ART and sexual preferences. The effect was found at quantitative levels of several molecular agents and active bacteria which were herein identified and whose abundance correlated with HIV immune pathogenesis markers. Although, we cannot rule out the possibility that some changes are partially a random consequence of the disease status, our data suggest that most likely reduced inflammation and immune recovery is a joint solution orchestrated by both the active fraction of the gut microbiota and the host. Elsevier 2016-04-27 /pmc/articles/PMC4919658/ /pubmed/27428431 http://dx.doi.org/10.1016/j.ebiom.2016.04.033 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Paper Serrano-Villar, Sergio Rojo, David Martínez-Martínez, Mónica Deusch, Simon Vázquez-Castellanos, Jorge F. Bargiela, Rafael Sainz, Talía Vera, Mar Moreno, Santiago Estrada, Vicente Gosalbes, María José Latorre, Amparo Seifert, Jana Barbas, Coral Moya, Andrés Ferrer, Manuel Gut Bacteria Metabolism Impacts Immune Recovery in HIV-infected Individuals |
title | Gut Bacteria Metabolism Impacts Immune Recovery in HIV-infected Individuals |
title_full | Gut Bacteria Metabolism Impacts Immune Recovery in HIV-infected Individuals |
title_fullStr | Gut Bacteria Metabolism Impacts Immune Recovery in HIV-infected Individuals |
title_full_unstemmed | Gut Bacteria Metabolism Impacts Immune Recovery in HIV-infected Individuals |
title_short | Gut Bacteria Metabolism Impacts Immune Recovery in HIV-infected Individuals |
title_sort | gut bacteria metabolism impacts immune recovery in hiv-infected individuals |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4919658/ https://www.ncbi.nlm.nih.gov/pubmed/27428431 http://dx.doi.org/10.1016/j.ebiom.2016.04.033 |
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