A Repeat-Associated Small RNA Controls the Major Virulence Factors of Helicobacter pylori

Mol Cell. 2020 Oct 15;80(2):210-226.e7. doi: 10.1016/j.molcel.2020.09.009. Epub 2020 Sep 30.

Abstract

Many bacterial pathogens regulate their virulence genes via phase variation, whereby length-variable simple sequence repeats control the transcription or coding potential of those genes. Here, we have exploited this relationship between DNA structure and physiological function to discover a globally acting small RNA (sRNA) regulator of virulence in the gastric pathogen Helicobacter pylori. Our study reports the first sRNA whose expression is affected by a variable thymine (T) stretch in its promoter. We show the sRNA post-transcriptionally represses multiple major pathogenicity factors of H. pylori, including CagA and VacA, by base pairing to their mRNAs. We further demonstrate transcription of the sRNA is regulated by the nickel-responsive transcriptional regulator NikR (thus named NikS for nickel-regulated sRNA), thereby linking virulence factor regulation to nickel concentrations. Using in-vitro infection experiments, we demonstrate NikS affects host cell internalization and epithelial barrier disruption. Together, our results show NikS is a phase-variable, post-transcriptional global regulator of virulence properties in H. pylori.

Keywords: CagA; Helicobacter pylori; VacA regulatory networks; phase-variation; post-transcriptional regulation; simple sequence repeats; small regulatory RNA; virulence factors; virulence regulator.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins / metabolism
  • Base Sequence
  • Colony Count, Microbial
  • Endocytosis / drug effects
  • Gene Deletion
  • Gene Expression Regulation, Bacterial / drug effects
  • Helicobacter pylori / drug effects
  • Helicobacter pylori / genetics*
  • Helicobacter pylori / pathogenicity*
  • Host-Pathogen Interactions / drug effects
  • Nickel / pharmacology
  • Phenotype
  • Promoter Regions, Genetic
  • RNA, Bacterial / genetics*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Repetitive Sequences, Nucleic Acid / genetics*
  • Transcription, Genetic / drug effects
  • Virulence Factors / metabolism*

Substances

  • Bacterial Proteins
  • RNA, Bacterial
  • RNA, Messenger
  • Virulence Factors
  • Nickel