The read-through transcription-mediated autoactivation circuit for virulence regulator expression drives robust type III secretion system 2 expression in Vibrio parahaemolyticus

PLoS Pathog. 2024 Mar 27;20(3):e1012094. doi: 10.1371/journal.ppat.1012094. eCollection 2024 Mar.

Abstract

Vibrio parahaemolyticus is the leading cause of seafood-borne gastroenteritis in humans worldwide. The major virulence factor responsible for the enteropathogenicity of this pathogen is type III secretion system 2 (T3SS2), which is encoded on the 80-kb V. parahaemolyticus pathogenicity island (Vp-PAI), the gene expression of which is governed by the OmpR-family transcriptional regulator VtrB. Here, we found a positive autoregulatory feature of vtrB transcription, which is often observed with transcriptional regulators of bacteria, but the regulation was not canonically dependent on its own promoter. Instead, this autoactivation was induced by heterogeneous transcripts derived from the VtrB-regulated operon upstream of vtrB. VtrB-activated transcription overcame the intrinsic terminator downstream of the operon, resulting in transcription read-through with read-in transcription of the vtrB gene and thus completing the autoregulatory loop for vtrB gene expression. The dampening of read-through transcription with an exogenous strong terminator reduced vtrB gene expression. Furthermore, a V. parahaemolyticus mutant with defects in the vtrB autoregulatory loop also showed compromises in T3SS2 expression and T3SS2-dependent cytotoxicity in vitro and enterotoxicity in vivo, indicating that this autoregulatory loop is essential for sustained vtrB activation and the consequent robust expression of T3SS2 genes for pathogenicity. Taken together, these findings demonstrate that the regulatory loop for vtrB gene expression based on read-through transcription from the upstream operon is a crucial pathway in T3SS2 gene regulatory network to ensure T3SS2-mediated virulence of V. parahaemolyticus.

MeSH terms

  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Gene Expression Regulation, Bacterial
  • Humans
  • Promoter Regions, Genetic
  • Type III Secretion Systems / genetics
  • Type III Secretion Systems / metabolism
  • Vibrio Infections* / genetics
  • Vibrio Infections* / microbiology
  • Vibrio parahaemolyticus*
  • Virulence / genetics
  • Virulence Factors / genetics
  • Virulence Factors / metabolism

Substances

  • Type III Secretion Systems
  • Virulence Factors
  • Bacterial Proteins

Grants and funding

This study was supported by Grants-in-Aid for Scientific Research from the Japan Society for the Promotion of Science (Grants 20K07428 and 23K06529 to S.M. and Grants 20K15748 and 23K05637 to E.I.), the Institute for Fermentation (to S.M.), the Chemo-Sero-Therapeutic Research Institute (to S.M.), the Joint Usage / Research Center on Tropical Disease, Institute of Tropical Medicine, Nagasaki University (2023-Ippan-14 to S.M.), the Center for Infectious Disease Education and Research (to S.M. and E.I.), and by the Taniguchi scholarship program from BIKEN Foundation (to D.S.A.). The funders had no role in study design, data collection, and interpretation, or the decision to submit the work for publication.