Exploration of Salmonella effector mutant strains on MTR4 and RRP6 degradation.
Bacterial Proteins
/ genetics
Exoribonucleases
/ metabolism
Exosome Multienzyme Ribonuclease Complex
/ metabolism
HeLa Cells
Host-Pathogen Interactions
/ genetics
Humans
Membrane Proteins
/ genetics
Mutation
Proteolysis
RNA Helicases
/ metabolism
RNA, Bacterial
/ metabolism
RNA, Nuclear
/ metabolism
Salmonella Food Poisoning
/ microbiology
Salmonella typhimurium
/ genetics
Type III Secretion Systems
/ genetics
Virulence
/ genetics
Virulence Factors
/ genetics
Flagella
MTR4
RRP6
SPI-1
SPI-2
T3SSs
Journal
Bioscience trends
ISSN: 1881-7823
Titre abrégé: Biosci Trends
Pays: Japan
ID NLM: 101502754
Informations de publication
Date de publication:
21 Sep 2020
21 Sep 2020
Historique:
pubmed:
1
5
2020
medline:
6
7
2021
entrez:
1
5
2020
Statut:
ppublish
Résumé
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.
Identifiants
pubmed: 32350160
doi: 10.5582/bst.2020.03085
doi:
Substances chimiques
Bacterial Proteins
0
Membrane Proteins
0
RNA, Bacterial
0
RNA, Nuclear
0
SPI-2 protein, Salmonella
0
Spi1 protein, Salmonella
0
Type III Secretion Systems
0
Virulence Factors
0
Exoribonucleases
EC 3.1.-
Exosome Multienzyme Ribonuclease Complex
EC 3.1.-
EXOSC10 protein, human
EC 3.1.13.-
MTREX protein, human
EC 3.6.1.-
RNA Helicases
EC 3.6.4.13
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM