Airway epithelial CD47 plays a critical role in inducing influenza virus-mediated bacterial super-infection

Nat Commun. 2024 Apr 30;15(1):3666. doi: 10.1038/s41467-024-47963-5.

Abstract

Respiratory viral infection increases host susceptibility to secondary bacterial infections, yet the precise dynamics within airway epithelia remain elusive. Here, we elucidate the pivotal role of CD47 in the airway epithelium during bacterial super-infection. We demonstrated that upon influenza virus infection, CD47 expression was upregulated and localized on the apical surface of ciliated cells within primary human nasal or bronchial epithelial cells. This induced CD47 exposure provided attachment sites for Staphylococcus aureus, thereby compromising the epithelial barrier integrity. Through bacterial adhesion assays and in vitro pull-down assays, we identified fibronectin-binding proteins (FnBP) of S. aureus as a key component that binds to CD47. Furthermore, we found that ciliated cell-specific CD47 deficiency or neutralizing antibody-mediated CD47 inactivation enhanced in vivo survival rates. These findings suggest that interfering with the interaction between airway epithelial CD47 and pathogenic bacterial FnBP holds promise for alleviating the adverse effects of super-infection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacterial Adhesion
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Bronchi / cytology
  • Bronchi / metabolism
  • CD47 Antigen* / genetics
  • CD47 Antigen* / metabolism
  • Epithelial Cells* / metabolism
  • Epithelial Cells* / microbiology
  • Epithelial Cells* / virology
  • Humans
  • Influenza A Virus, H1N1 Subtype
  • Influenza, Human / immunology
  • Influenza, Human / metabolism
  • Influenza, Human / virology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Orthomyxoviridae Infections / immunology
  • Orthomyxoviridae Infections / metabolism
  • Orthomyxoviridae Infections / virology
  • Respiratory Mucosa / metabolism
  • Respiratory Mucosa / microbiology
  • Respiratory Mucosa / virology
  • Staphylococcal Infections* / immunology
  • Staphylococcal Infections* / metabolism
  • Staphylococcal Infections* / microbiology
  • Staphylococcus aureus*
  • Superinfection* / microbiology

Substances

  • CD47 Antigen
  • CD47 protein, human
  • Bacterial Proteins