Exploration of Salmonella effector mutant strains on MTR4 and RRP6 degradation

Biosci Trends. 2020 Sep 21;14(4):255-262. doi: 10.5582/bst.2020.03085. Epub 2020 Apr 30.

Abstract

Salmonella enterica serovar Typhimurium (Salmonella), a pathogenic bacterium, is a major cause of foodborne diseases worldwide. Salmonella injects multiple virulence factors, called effectors, into cells and causes multiple rearrangements of cellular biological reactions that are important for Salmonella proliferation and virulence. Previously, we reported that Salmonella infection causes loss of MTR4 and RRP6, which are nuclear RNA degradation factors, resulting in the stabilization and accumulation of unstable nuclear RNAs. This accumulation is important for the cellular defense for Salmonella infection. In this study, we examined a series of Salmonella mutant strains, most of which are strains with genes related to effectors translocated by T3SSs encoded on Salmonella pathogenic islands, SPI-1 and SPI-2, that have been depleted. Among 42 Salmonella mutants, 6 mutants' infections canceled loss of MTR4 and RRP6. Proliferation assay of Salmonella in the cell revealed that six mutants showed poor proliferation in the host cell, demonstrating that poor proliferation contributed to cancellation of MTR4 and RRP6 loss. This result indicates that certain events associated with Salmonella proliferation in host cells cause loss of MTR4 and RRP6.

Keywords: Flagella; MTR4; RRP6; SPI-1; SPI-2; T3SSs.

MeSH terms

  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Exoribonucleases / metabolism*
  • Exosome Multienzyme Ribonuclease Complex / metabolism*
  • HeLa Cells
  • Host-Pathogen Interactions / genetics
  • Humans
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Mutation
  • Proteolysis
  • RNA Helicases / metabolism*
  • RNA, Bacterial / metabolism
  • RNA, Nuclear / metabolism
  • Salmonella Food Poisoning / microbiology*
  • Salmonella typhimurium / genetics
  • Salmonella typhimurium / pathogenicity*
  • Type III Secretion Systems / genetics
  • Type III Secretion Systems / metabolism
  • Virulence / genetics
  • Virulence Factors / genetics*
  • Virulence Factors / metabolism

Substances

  • Bacterial Proteins
  • Membrane Proteins
  • RNA, Bacterial
  • RNA, Nuclear
  • SPI-2 protein, Salmonella
  • Spi1 protein, Salmonella
  • Type III Secretion Systems
  • Virulence Factors
  • Exoribonucleases
  • Exosome Multienzyme Ribonuclease Complex
  • EXOSC10 protein, human
  • MTREX protein, human
  • RNA Helicases