Human tetraspanin CD81 facilitates invasion of Salmonella enterica into human epithelial cells

Virulence. 2024 Dec;15(1):2399792. doi: 10.1080/21505594.2024.2399792. Epub 2024 Sep 24.

Abstract

Human CD81 and CD9 are members of the tetraspanin family of proteins characterized by a canonical structure of four transmembrane domains and two extracellular loop domains. Tetraspanins are known as molecular facilitators, which assemble and organize cell surface receptors and partner molecules forming clusters known as tetraspanin-enriched microdomains. They have been implicated to play various biological roles including an involvement in infections with microbial pathogens. Here, we demonstrate an important role of CD81 for the invasion of epithelial cells by Salmonella enterica. We show that the overexpression of CD81 in HepG2 cells enhances invasion of various typhoidal and non-typhoidal Salmonella serovars. Deletion of CD81 by CRISPR/Cas9 in intestinal epithelial cells (C2BBe1 and HT29-MTX-E12) reduces S. Typhimurium invasion. In addition, the effect of human CD81 is species-specific as only human but not rat CD81 facilitates Salmonella invasion. Finally, immunofluorescence microscopy and proximity ligation assay revealed that both human tetraspanins CD81 and CD9 are recruited to the entry site of S. Typhimurium during invasion but not during adhesion to the host cell surface. Overall, we demonstrate that the human tetraspanin CD81 facilitates Salmonella invasion into epithelial host cells.

Keywords: Salmonella; infection; intestinal epithelium; invasion; tetraspanins.

MeSH terms

  • Animals
  • Epithelial Cells* / microbiology
  • HT29 Cells
  • Hep G2 Cells
  • Humans
  • Rats
  • Salmonella Infections / microbiology
  • Salmonella enterica* / genetics
  • Salmonella enterica* / physiology
  • Salmonella typhimurium / genetics
  • Salmonella typhimurium / metabolism
  • Salmonella typhimurium / pathogenicity
  • Salmonella typhimurium / physiology
  • Tetraspanin 28* / genetics
  • Tetraspanin 28* / metabolism
  • Tetraspanin 29* / genetics
  • Tetraspanin 29* / metabolism

Substances

  • Tetraspanin 28
  • CD81 protein, human
  • Tetraspanin 29
  • CD9 protein, human

Grants and funding

This work was supported by the Deutsche Forschungsgemeinschaft (DFG) collaborative research center SFB 900 [Project number 158989968] to GAG, TK, and GG. KGA was supported by the German Academic Exchange Service DAAD, the Hannover Biomedical Research School (HBRS) and by the Center for Infection Biology (ZIB). This work was also funded by the Ministry of Science and Culture of Lower Saxony and the German Federal Ministry of Education and Research through the Professorinnenprogramm III and the Knut and Alice Wallenberg Foundation to GG.