Cells (Feb 2021)

Gut Microbiome Profiles and Associated Metabolic Pathways in HIV-Infected Treatment-Naïve Patients

  • Wellinton M. do Nascimento,
  • Aline Machiavelli,
  • Luiz G. E. Ferreira,
  • Luisa Cruz Silveira,
  • Suwellen S. D. de Azevedo,
  • Gonzalo Bello,
  • Daniel P. Smith,
  • Melissa P. Mezzari,
  • Joseph F. Petrosino,
  • Rubens Tadeu Delgado Duarte,
  • Carlos R. Zárate-Bladés,
  • Aguinaldo R. Pinto

DOI
https://doi.org/10.3390/cells10020385
Journal volume & issue
Vol. 10, no. 2
p. 385

Abstract

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The normal composition of the intestinal microbiota is a key factor for maintaining healthy homeostasis, and accordingly, dysbiosis is well known to be present in HIV-1 patients. This article investigates the gut microbiota profile of antiretroviral therapy-naive HIV-1 patients and healthy donors living in Latin America in a cohort of 13 HIV positive patients (six elite controllers, EC, and seven non-controllers, NC) and nine healthy donors (HD). Microbiota compositions in stool samples were determined by sequencing the V3-V4 region of the bacterial 16S rRNA, and functional prediction was inferred using PICRUSt. Several taxa were enriched in EC compared to NC or HD groups, including Acidaminococcus, Clostridium methylpentosum, Barnesiella, Eubacterium coprostanoligenes, and Lachnospiraceae UCG-004. In addition, our data indicate that the route of infection is an important factor associated with changes in gut microbiome composition, and we extend these results by identifying several metabolic pathways associated with each route of infection. Importantly, we observed several bacterial taxa that might be associated with different viral subtypes, such as Succinivibrio, which were more abundant in patients infected by HIV subtype B, and Streptococcus enrichment in patients infected by subtype C. In conclusion, our data brings a significant contribution to the understanding of dysbiosis-associated changes in HIV infection and describes, for the first time, differences in microbiota composition according to HIV subtypes. These results warrant further confirmation in a larger cohort of patients.

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