Home LiteratureArticle Details
PMID: 9421907 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Exponential-phase expression of spvA of the Salmonella typhimurium virulence plasmid: induction in intracellular salts medium and intracellularly in mice and cultured mammalian cells.

Microbiology (Reading, England) ·Vol. 143 ( Pt 12) ·1997-12-00 ·Pages 3827-3839

Wilson JA, Doyle TJ, Gulig PA

Abstract

The spv genes of Salmonella typhimurium and other non-typhoidal Salmonella serovars are essential for efficient systemic infection beyond the intestines in orally inoculated mice as a model for enteric fever. These virulence genes are not significantly expressed by salmonellae during exponential growth in L broth but are induced when the bacteria enter the stationary phase of growth. Using RNase protection analysis to directly measure spvA mRNA from the virulence plasmid of S. typhimurium, we found that spvA was maximally induced in an SpvR- and RpoS-dependent manner during exponential growth in intracellular Salts Medium, which mimics the intracellular environment of mammalian cells. A cloned spvA-lacZ operon fusion in S. typhimurium was induced intracellularly in periotoneal cells of mice, correlating in vivo intracellular gene expression with intracellular function of the spv genes in infected mice. spvA was also induced intracellularly in vitro within both Henle-407 intestinal epithelial cells and J774.A1 macrophage-like cells when the bacteria were replicating with exponential kinetics. Prevention of invasion of salmonellae with cytochalasin D inhibited spvA induction within tissue culture cells, indicating that salmonellae must be internalized for spvA to be induced. The spvA-lacZ fusion was not induced by salmonellae in extracellular fluid of the peritoneal cavity or in serum. Since induction of the spv genes occurs intracellularly during exponential growth of salmonellae, cessation of growth may not be the most relevant inducing signal for spv gene expression.

MeSH Terms
Animals Base Sequence Cell Line Gene Expression Regulation, Bacterial Genes, Bacterial Humans Intestinal Mucosa Mammals Mice Operon Plasmids RNA, Messenger/biosynthesis Rats Recombinant Fusion Proteins/biosynthesis Restriction Mapping Salmonella Infections, Animal/microbiology Salmonella typhimurium/genetics,growth & development,pathogenicity Transcription, Genetic Transfection Virulence/genetics
Chemicals
RNA, Messenger Recombinant Fusion Proteins
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Wilson Julie A
Doyle Thomas J
Department of Molecular Genetics and Microbiology, University of Florida College of Medicine, Gainesville, FL 32610-0266, USA.
Gulig Paul A
Department of Molecular Genetics and Microbiology, University of Florida College of Medicine, Gainesville, FL 32610-0266, USA.
Article Info
Journal
Microbiology (Reading, England)
Abbr.
Microbiology (Reading)
ISSN
1350-0872
Published
1997-12-00
Pages
3827-3839
Language
English
Region
England
NLM ID
9430468
Subset
IM
Grants
NIAID NIH HHS · AI24821 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com