» Articles » PMID: 30531898

The Small RNA RssR Regulates Myo-inositol Degradation by Salmonella Enterica

Overview
Journal Sci Rep
Specialty Science
Date 2018 Dec 12
PMID 30531898
Citations 9
Authors
Affiliations
Soon will be listed here.
Abstract

Small noncoding RNAs (sRNAs) with putative regulatory functions in gene expression have been identified in the enteropathogen Salmonella enterica serovar Typhimurium (S. Typhimurium). Two sRNAs are encoded by the genomic island GEI4417/4436 responsible for myo-inositol (MI) degradation, suggesting a role in the regulation of this metabolic pathway. We show that a lack of the sRNA STnc2160, termed RssR, results in a severe growth defect in minimal medium (MM) with MI. In contrast, the second sRNA STnc1740 was induced in the presence of glucose, and its overexpression slightly attenuated growth in the presence of MI. Constitutive expression of RssR led to an increased stability of the reiD mRNA, which encodes an activator of iol genes involved in MI utilization, via interaction with its 5'-UTR. SsrB, a response regulator contributing to the virulence properties of salmonellae, activated rssR transcription by binding the sRNA promoter. In addition, the absence of the RNA chaperone Hfq resulted in strongly decreased levels of RssR, attenuated S. Typhimurium growth with MI, and reduced expression of several iol genes required for MI degradation. Considered together, the extrinsic RssR allows fine regulation of cellular ReiD levels and thus of MI degradation by acting on the reiD mRNA stability.

Citing Articles

DNA concentrations in amniotic fluid according to gestational age and fetal sex: data from 2573 samples.

Gofin Y, Svirsky R, Lavi Ben Atav D, Liberman M, Tenne T, Perlman S Arch Gynecol Obstet. 2024; 310(4):1981-1987.

PMID: 39210070 PMC: 11393111. DOI: 10.1007/s00404-024-07698-6.


Nitrosative stress under microaerobic conditions triggers inositol metabolism in Pseudomonas extremaustralis.

Venero E, Giambartolomei L, Sosa E, Fernandez do Porto D, Lopez N, Tribelli P PLoS One. 2024; 19(5):e0301252.

PMID: 38696454 PMC: 11065229. DOI: 10.1371/journal.pone.0301252.


Shear Histories Alter Local Shear Effects on Thrombus Nucleation and Growth.

Kang J, Jayaraman A, Antaki J, Kirby B Ann Biomed Eng. 2024; 52(4):1039-1050.

PMID: 38319505 DOI: 10.1007/s10439-023-03439-z.


Hierarchic regulation of a metabolic pathway: H-NS, CRP, and SsrB control -inositol utilization by .

Felsl A, Brokatzky D, Kroger C, Heermann R, Fuchs T Microbiol Spectr. 2023; 12(1):e0272423.

PMID: 38095474 PMC: 10783015. DOI: 10.1128/spectrum.02724-23.


Physiological characteristics and virulence gene composition of selected serovars of seafood-borne .

Salam F, Lekshmi M, Prabhakar P, Kumar S, Nayak B Vet World. 2023; 16(3):431-438.

PMID: 37041837 PMC: 10082740. DOI: 10.14202/vetworld.2023.431-438.


References
1.
Chao Y, Li L, Girodat D, Forstner K, Said N, Corcoran C . In Vivo Cleavage Map Illuminates the Central Role of RNase E in Coding and Non-coding RNA Pathways. Mol Cell. 2017; 65(1):39-51. PMC: 5222698. DOI: 10.1016/j.molcel.2016.11.002. View

2.
Zuker M . Mfold web server for nucleic acid folding and hybridization prediction. Nucleic Acids Res. 2003; 31(13):3406-15. PMC: 169194. DOI: 10.1093/nar/gkg595. View

3.
Walthers D, Li Y, Liu Y, Anand G, Yan J, Kenney L . Salmonella enterica response regulator SsrB relieves H-NS silencing by displacing H-NS bound in polymerization mode and directly activates transcription. J Biol Chem. 2010; 286(3):1895-902. PMC: 3023485. DOI: 10.1074/jbc.M110.164962. View

4.
Eriksson S, Lucchini S, Thompson A, Rhen M, Hinton J . Unravelling the biology of macrophage infection by gene expression profiling of intracellular Salmonella enterica. Mol Microbiol. 2002; 47(1):103-18. DOI: 10.1046/j.1365-2958.2003.03313.x. View

5.
Feng X, Walthers D, Oropeza R, Kenney L . The response regulator SsrB activates transcription and binds to a region overlapping OmpR binding sites at Salmonella pathogenicity island 2. Mol Microbiol. 2004; 54(3):823-35. DOI: 10.1111/j.1365-2958.2004.04317.x. View