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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
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.
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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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