TY - JOUR
T1 - Evolution of the gut microbiome following acute HIV-1 infection
AU - Rocafort, Muntsa
AU - Noguera-Julian, Marc
AU - Rivera, Javier
AU - Pastor, Lucía
AU - Guillén, Yolanda
AU - Langhorst, Jost
AU - Parera, Mariona
AU - Mandomando, Inacio
AU - Carrillo, Jorge
AU - Urrea, Víctor
AU - Rodríguez, Cristina
AU - Casadellà, Maria
AU - Calle, Maria Luz
AU - Clotet, Bonaventura
AU - Blanco, Julià
AU - Naniche, Denise
AU - Paredes, Roger
PY - 2019/5/11
Y1 - 2019/5/11
N2 - © 2019 The Author(s). Background: In rhesus macaques, simian immunodeficiency virus infection is followed by expansion of enteric viruses but has a limited impact on the gut bacteriome. To understand the longitudinal effects of HIV-1 infection on the human gut microbiota, we prospectively followed 49 Mozambican subjects diagnosed with recent HIV-1 infection (RHI) and 54 HIV-1-negative controls for 9-18 months and compared them with 98 chronically HIV-1-infected subjects treated with antiretrovirals (n = 27) or not (n = 71). Results: We show that RHI is followed by increased fecal adenovirus shedding, which persists during chronic HIV-1 infection and does not resolve with ART. Recent HIV-1 infection is also followed by transient non-HIV-specific changes in the gut bacterial richness and composition. Despite early resilience to change, an HIV-1-specific signature in the gut bacteriome - featuring depletion of Akkermansia, Anaerovibrio, Bifidobacterium, and Clostridium - previously associated with chronic inflammation, CD8+ T cell anergy, and metabolic disorders, can be eventually identified in chronically HIV-1-infected subjects. Conclusions: Recent HIV-1 infection is associated with increased fecal shedding of eukaryotic viruses, transient loss of bacterial taxonomic richness, and long-term reductions in microbial gene richness. An HIV-1-associated microbiome signature only becomes evident in chronically HIV-1-infected subjects.
AB - © 2019 The Author(s). Background: In rhesus macaques, simian immunodeficiency virus infection is followed by expansion of enteric viruses but has a limited impact on the gut bacteriome. To understand the longitudinal effects of HIV-1 infection on the human gut microbiota, we prospectively followed 49 Mozambican subjects diagnosed with recent HIV-1 infection (RHI) and 54 HIV-1-negative controls for 9-18 months and compared them with 98 chronically HIV-1-infected subjects treated with antiretrovirals (n = 27) or not (n = 71). Results: We show that RHI is followed by increased fecal adenovirus shedding, which persists during chronic HIV-1 infection and does not resolve with ART. Recent HIV-1 infection is also followed by transient non-HIV-specific changes in the gut bacterial richness and composition. Despite early resilience to change, an HIV-1-specific signature in the gut bacteriome - featuring depletion of Akkermansia, Anaerovibrio, Bifidobacterium, and Clostridium - previously associated with chronic inflammation, CD8+ T cell anergy, and metabolic disorders, can be eventually identified in chronically HIV-1-infected subjects. Conclusions: Recent HIV-1 infection is associated with increased fecal shedding of eukaryotic viruses, transient loss of bacterial taxonomic richness, and long-term reductions in microbial gene richness. An HIV-1-associated microbiome signature only becomes evident in chronically HIV-1-infected subjects.
KW - AIDS
KW - HIV-1
KW - HIV-1 pathogenesis
KW - Microbiome
KW - acute HIV-1 infection
UR - http://www.mendeley.com/research/evolution-gut-microbiome-following-acute-hiv1-infection
U2 - 10.1186/s40168-019-0687-5
DO - 10.1186/s40168-019-0687-5
M3 - Article
C2 - 31078141
SN - 2049-2618
VL - 7
JO - Microbiome
JF - Microbiome
M1 - 73
ER -