Toll-like receptors, environmental caging, and lung dysbiosis

Am J Physiol Lung Cell Mol Physiol. 2021 Aug 1;321(2):L404-L415. doi: 10.1152/ajplung.00002.2021. Epub 2021 Jun 23.

Abstract

Recent studies have implicated lung microbiota in shaping local alveolar immune responses. Toll-like receptors are major sensors of microbiota and determinants of local epithelial homeostasis. The impact of toll-like receptor deficiency on lung microbiota is unknown. To determine whether the absence of toll-like receptors results in altered lung microbiota or dysbiosis, we compared lung microbiota in wild-type and toll-like receptor-deficient experimental mice using 16S ribosomal RNA gene quantification and sequencing. We used a randomized environmental caging strategy to determine the impact of toll-like receptors on lung microbiota. Lung microbiota are detectable in toll-like receptor-deficient experimental mice and exhibit considerable variability. The lung microbiota of toll-like receptor-deficient mice are altered in community composition (PERMANOVA P < 0.001), display reduced diversity (t test P = 0.0075), and bacterial burden (t test P = 0.016) compared with wild-type mice with intact toll-like receptors and associated signaling pathways. The lung microbiota of wild-type mice when randomized to cages with toll-like receptor-deficient mice converged with no significant difference in community composition (PERMANOVA P > 0.05) after 3 wk of cohousing. The lung microbiome of toll-like receptor-deficient mice is distinct from wild-type mice and may be less susceptible to the effects of caging as an environmental variable. Our observations support a role for toll-like receptor signaling in the shaping of lung microbiota.

Keywords: cage; lung microbiome; toll-like receptors.

Publication types

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

MeSH terms

  • Animals
  • Bacteria* / classification
  • Bacteria* / genetics
  • Bacteria* / growth & development
  • Dysbiosis / genetics
  • Dysbiosis / microbiology*
  • Dysbiosis / pathology
  • Lung / microbiology*
  • Lung / pathology
  • Mice
  • Microbiota*
  • RNA, Bacterial / genetics
  • RNA, Ribosomal, 16S / genetics
  • Toll-Like Receptors / deficiency*
  • Toll-Like Receptors / metabolism

Substances

  • RNA, Bacterial
  • RNA, Ribosomal, 16S
  • Toll-Like Receptors