Exploration of Salmonella effector mutant strains on MTR4 and RRP6 degradation.


Journal

Bioscience trends
ISSN: 1881-7823
Titre abrégé: Biosci Trends
Pays: Japan
ID NLM: 101502754

Informations de publication

Date de publication:
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

Pagination

255-262

Auteurs

Xiaoning Sun (X)

Isotope Science Center, The University of Tokyo, Tokyo, Japan.
Advanced Interdisciplinary Studies, Engineering Department, The University of Tokyo, Tokyo, Japan.

Kentaro Kawata (K)

Isotope Science Center, The University of Tokyo, Tokyo, Japan.

Atsuko Miki (A)

Isotope Science Center, The University of Tokyo, Tokyo, Japan.

Youichiro Wada (Y)

Isotope Science Center, The University of Tokyo, Tokyo, Japan.
Advanced Interdisciplinary Studies, Engineering Department, The University of Tokyo, Tokyo, Japan.

Masami Nagahama (M)

Laboratory of Molecular and Cellular Biochemistry, Meiji Pharmaceutical University, Tokyo, Japan.

Akiko Takaya (A)

Department of Natural Products Chemistry, Graduate School of Pharmaceutical Sciences, Chiba University, Chiba, Japan.
Medical Mycology Research Center, Chiba University, Chiba, Japan.

Nobuyoshi Akimitsu (N)

Isotope Science Center, The University of Tokyo, Tokyo, Japan.

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Classifications MeSH