Frontiers in Microbiology (Feb 2023)

Topography of respiratory tract and gut microbiota in mice with influenza A virus infection

  • Qichao Chen,
  • Qichao Chen,
  • Manjiao Liu,
  • Manjiao Liu,
  • Yanfeng Lin,
  • Yanfeng Lin,
  • Kaiying Wang,
  • Jinhui Li,
  • Peihan Li,
  • Lang Yang,
  • Leili Jia,
  • Bei Zhang,
  • Bei Zhang,
  • Hao Guo,
  • Hao Guo,
  • Peng Li,
  • Hongbin Song,
  • Hongbin Song

DOI
https://doi.org/10.3389/fmicb.2023.1129690
Journal volume & issue
Vol. 14

Abstract

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IntroductionInfluenza A virus (IAV)-induced dysbiosis may predispose to severe bacterial superinfections. Most studies have focused on the microbiota of single mucosal surfaces; consequently, the relationships between microbiota at different anatomic sites in IAV-infected mice have not been fully studied.MethodsWe characterized respiratory and gut microbiota using full-length 16S rRNA gene sequencing by Nanopore sequencers and compared the nasopharyngeal, oropharyngeal, lung and gut microbiomes in healthy and IAV-infected mice.ResultsThe oropharyngeal, lung and gut microbiota of healthy mice were dominated by Lactobacillus spp., while nasopharyngeal microbiota were comprised primarily of Streptococcus spp. However, the oropharyngeal, nasopharyngeal, lung, and gut microbiota of IAV-infected mice were dominated by Pseudomonas, Escherichia, Streptococcus, and Muribaculum spp., respectively. Lactobacillus murinus was identified as a biomarker and was reduced at all sites in IAV-infected mice. The microbiota composition of lung was more similar to that of the nasopharynx than the oropharynx in healthy mice.DiscussionThese findings suggest that the main source of lung microbiota in mice differs from that of adults. Moreover, the similarity between the nasopharyngeal and lung microbiota was increased in IAV-infected mice. We found that IAV infection reduced the similarity between the gut and oropharyngeal microbiota. L. murinus was identified as a biomarker of IAV infection and may be an important target for intervention in post-influenza bacterial superinfections.

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