Compositional analyses reveal correlations between taxon-level gut bacterial abundance and peripheral T cell marker expression in African infants

Gut Microbes. 2020;11(2):237-244. doi: 10.1080/19490976.2019.1643673. Epub 2019 Jul 26.

Abstract

Although exclusive breastfeeding has been linked to lower rates of postnatal HIV transmission compared to nonexclusive breastfeeding, mechanisms underlying this are unclear. Across a longitudinally sampled cohort of South African infants, we showed that exclusively breastfed (EBF) infants had altered gut bacterial communities when compared to nonexclusively breastfed (NEBF) infants, as well as reduced peripheral CD4 + T cell activation and lowered chemokine and chemokine receptor expression in the oral mucosa. We further demonstrated that the relative abundance of key taxa was correlated with peripheral CD4 + T cell activation. Here, we supplement those findings by using compositional data analyses to identify shifts in the abundance of several Bifidobacteria strains relative to select strains of Escherichia, Bacteroides, and others that are associated with the transition to NEBF. We illustrate that the abundance ratio of these taxa is tightly correlated with feeding modality and is a strong predictor of peripheral T cell activation. More broadly, we discuss our study in the context of novel developments and explore future directions for the field.

Keywords: Bacterial microbiota; South Africa; T cell activation; compositional transform; feeding; mucosal gene expression.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Bacteria / classification*
  • Bacteria / genetics
  • Bacteria / isolation & purification
  • Bacteroides / genetics
  • Bacteroides / isolation & purification
  • Bifidobacterium / genetics
  • Bifidobacterium / isolation & purification
  • Breast Feeding*
  • CD4 Lymphocyte Count
  • Cohort Studies
  • Escherichia / genetics
  • Escherichia / isolation & purification
  • Gastrointestinal Microbiome* / genetics
  • Gastrointestinal Microbiome* / immunology
  • Genes, Bacterial
  • HIV Infections / immunology
  • HIV Infections / transmission
  • Humans
  • Infant
  • Infant, Newborn
  • Infectious Disease Transmission, Vertical
  • Intraepithelial Lymphocytes / metabolism*
  • Longitudinal Studies
  • Metagenomics
  • Mouth Mucosa / immunology
  • Mouth Mucosa / metabolism
  • Mouth Mucosa / microbiology
  • Principal Component Analysis
  • RNA, Ribosomal, 16S / genetics
  • Receptors, Chemokine / metabolism
  • South Africa / epidemiology
  • T-Lymphocyte Subsets / metabolism

Substances

  • RNA, Ribosomal, 16S
  • Receptors, Chemokine