Salmonella adhesion is decreased by hypoxia due to adhesion and motility structure crosstalk

Vet Res. 2023 Oct 24;54(1):99. doi: 10.1186/s13567-023-01233-2.

Abstract

Initial stages of Salmonella Typhimurium infection involve a series of coordinated events aimed at reaching, attaching to, and invading host cells. Virulence factors such as flagella, fimbriae, and secretion systems play crucial roles in these events and are regulated in response to the host environment. The first point of contact between the pathogen and host is the intestinal epithelial layer, which normally serves as a barrier against invading pathogens, but can also be an entry site for pathogens. The integrity of this barrier can be modulated by the hypoxic environment of the intestines, created by the presence of trillions of microbes. Variable oxygen concentrations can strongly affect many functions of the gut, including secretion of cytokines and growth factors from the host site and affect the ability of Salmonella to persist, invade, and replicate. In this study, we investigated the first stages of Salmonella Typhimurium infection under hypoxic conditions in vitro and found that low oxygen levels significantly decreased bacterial adhesion. Using adhesion and motility assays, biofilm formation tests, as well as gene expression and cytokine secretion analysis, we identified a hypoxia-specific cross-talk between the expression of type 1 fimbriae and flagella, suggesting that altered flagellin expression levels affect the motility of bacteria and further impact their adhesion level, biofilm formation ability, and innate immune response. Overall, understanding how Salmonella interacts with its variable host environment provides insights into the virulence mechanisms of the bacterium and information regarding strategies for preventing or treating infections. Further research is required to fully understand the complex interplay between Salmonella and its host environment.

Keywords: Salmonella; adhesion; flagella; hypoxia; infection; microbiome; motility; type 1 fimbriae.

MeSH terms

  • Animals
  • Bacterial Adhesion
  • Bacterial Proteins / genetics
  • Flagellin*
  • Hypoxia / veterinary
  • Oxygen / metabolism
  • Salmonella typhimurium* / genetics
  • Virulence Factors / metabolism

Substances

  • Flagellin
  • Virulence Factors
  • Oxygen
  • Bacterial Proteins