A specific structure and high richness characterize intestinal microbiota of HIV-exposed seronegative individuals

ABSTRACT: Intestinal microbiota facilitates food breakdown for energy metabolism and influences the immune response, maintaining mucosal homeostasis. Overall, HIV infection is associated with intestinal dysbiosis and immune activation, which has been related to seroconversion in HIV-exposed individu...

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Autores:
Lopera Restrepo, Tulio José
Luján Tangarife, Jorge Armando
Zurek, Eduardo
Zapata Builes, Wildeman
Hernández López, Juan Carlos
Toro Londoño, Miguel Angel
Alzate Restrepo, Juan Fernando
Taborda Vanegas, Natalia Andrea
Rugeles López, María Teresa
Aguilar Jiménez, Wbeimar
Tipo de recurso:
Article of investigation
Fecha de publicación:
2021
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/29864
Acceso en línea:
https://hdl.handle.net/10495/29864
Palabra clave:
Microbioma Gastrointestinal
Gastrointestinal Microbiome
Infecciones por VIH - inmunología
HIV Infections - immunology
Infecciones por VIH - patología
HIV Infections - pathology
Linfocitos T Reguladores
T-Lymphocytes, Regulatory
Células Th17
Th17 Cells
Rights
openAccess
License
http://creativecommons.org/licenses/by/2.5/co/
Description
Summary:ABSTRACT: Intestinal microbiota facilitates food breakdown for energy metabolism and influences the immune response, maintaining mucosal homeostasis. Overall, HIV infection is associated with intestinal dysbiosis and immune activation, which has been related to seroconversion in HIV-exposed individuals. However, it is unclear whether microbiota dysbiosis is the cause or the effect of immune alterations and disease progression or if it could modulate the risk of acquiring the HIV infection. We characterize the intestinal microbiota and determine its association with immune regulation in HIV-exposed seronegative individuals (HESN), HIV-infected progressors (HIV+), and healthy control (HC) subjects. For this, feces and blood were collected. The microbiota composition of HESN showed a significantly higher alpha (p = 0.040) and beta diversity (p = 0.006) compared to HC, but no differences were found compared to HIV+. A lower Treg percentage was observed in HESN (1.77%) than HC (2.98%) and HIV+ (4.02%), with enrichment of the genus Butyrivibrio (p = 0.029) being characteristic of this profile. Moreover, we found that Megasphaera (p = 0.017) and Victivallis (p = 0.0029) also are enriched in the microbiota composition in HESN compared to HC and HIV+ subjects. Interestingly, an increase in Succinivibrio and Prevotella, and a reduction in Bacteroides genus, which is typical of HIV-infected individuals, were observed in both HESN and HIV+, compared to HC. Thus, HESNs have a microbiota profile, similar to that observed in HIV+, most likely because HESN are cohabiting with their HIV+ partners.