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Gut dysbiosis and inflammatory blood markers precede HIV with limited changes after early seroconversion

Authors :
Jennifer A. Fulcher
Fan Li
Nicole H. Tobin
Sara Zabih
Julie Elliott
Jesse L. Clark
Richard D'Aquila
Brian Mustanski
Michele D. Kipke
Steven Shoptaw
Pamina M. Gorbach
Grace M. Aldrovandi
Source :
eBioMedicine. 84:104286
Publication Year :
2022
Publisher :
Elsevier BV, 2022.

Abstract

BackgroundAlterations in the gut microbiome have been associated with HIV infection, but the relative impact of HIV versus other factors on the gut microbiome has been difficult to determine in cross-sectional studies.MethodsTo address this, we examined the gut microbiome, serum metabolome, and cytokines longitudinally within 27 individuals before and during acute HIV using samples collected from several ongoing cohort studies. Matched control participants (n=28) from the same cohort studies without HIV but at similar behavioral risk were used for comparison.FindingsWe identified few changes in the microbiome during acute HIV infection, but did find alterations in serum metabolites involving secondary bile acid (lithocholate sulfate, glycocholenate sulfate) and amino acid metabolism (3-methyl-2-oxovalerate, serine, cysteine, N-acetylputrescine). Greater microbiome differences, including decreased Bacteroides spp and increased Megasphaera elsdenii, were seen when comparing pre-HIV infection visits to matched at-risk controls. Those who acquired HIV also had elevated inflammatory cytokines (TNF-α, B cell activating factor, IL-8) and bioactive lipids (palmitoyl-sphingosine-phosphoethanolamide and glycerophosphoinositol) prior to HIV acquisition compared to matched controls.InterpretationLongitudinal sampling identified pre-existing microbiome differences in participants with acute HIV compared to matched control participants observed over the same period. These data highlight the importance of increasing understanding of the role of the microbiome in HIV susceptibility.FundingThis work was supported by NIH/NIAID (K08AI124979; P30AI117943), NIH/NIDA (U01DA036267; U01DA036939; U01DA036926; U24DA044554), and NIH/NIMH (P30MH058107; R34MH105272).

Details

ISSN :
23523964
Volume :
84
Database :
OpenAIRE
Journal :
eBioMedicine
Accession number :
edsair.doi.dedup.....c3a007b6aee85d270fe27c23b5236902
Full Text :
https://doi.org/10.1016/j.ebiom.2022.104286