An in vivo atlas of host-pathogen transcriptomes during Streptococcus pneumoniae colonization and disease

Proc Natl Acad Sci U S A. 2020 Dec 29;117(52):33507-33518. doi: 10.1073/pnas.2010428117. Epub 2020 Dec 14.

Abstract

Streptococcus pneumoniae (Spn) colonizes the nasopharynx and can cause pneumonia. From the lungs it spreads to the bloodstream and causes organ damage. We characterized the in vivo Spn and mouse transcriptomes within the nasopharynx, lungs, blood, heart, and kidneys using three Spn strains. We identified Spn genes highly expressed at all anatomical sites and in an organ-specific manner; highly expressed genes were shown to have vital roles with knockout mutants. The in vivo bacterial transcriptome during colonization/disease was distinct from previously reported in vitro transcriptomes. Distinct Spn and host gene-expression profiles were observed during colonization and disease states, revealing specific genes/operons whereby Spn adapts to and influences host sites in vivo. We identified and experimentally verified host-defense pathways induced by Spn during invasive disease, including proinflammatory responses and the interferon response. These results shed light on the pathogenesis of Spn and identify therapeutic targets.

Keywords: Streptococcus pneumoniae; dual species RNA-seq; host–pathogen interactions; in vivo transcriptomics; mouse models of colonization and invasive disease.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Colony Count, Microbial
  • Female
  • Gene Expression Regulation, Bacterial
  • Genes, Bacterial
  • Host-Pathogen Interactions / genetics*
  • Interferons / metabolism
  • Male
  • Mice, Inbred C57BL
  • Mutation / genetics
  • Phylogeny
  • Pneumococcal Infections / genetics*
  • Pneumococcal Infections / microbiology*
  • Principal Component Analysis
  • Signal Transduction
  • Streptococcus pneumoniae / growth & development
  • Streptococcus pneumoniae / physiology*
  • Transcriptome / genetics*

Substances

  • Interferons