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Microbiology 150 (2004), 3843-3855; DOI  10.1099/mic.0.27257-0
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Microbiology 150 (2004), 3843-3855; DOI  10.1099/mic.0.27257-0
© 2004 Society for General Microbiology

{sigma}B-dependent gene induction and expression in Listeria monocytogenes during osmotic and acid stress conditions simulating the intestinal environment

David Sue1, Daniel Fink2, Martin Wiedmann1 and Kathryn J. Boor1

1 Department of Food Science, Cornell University, Ithaca, NY 14853, USA
2 Department of Statistical Science, Cornell University, Ithaca, NY 14853, USA

Correspondence
Kathryn J. Boor
kjb4{at}cornell.edu

Listeria monocytogenes must overcome a variety of stress conditions in the host digestive tract to cause foodborne infections. The alternative sigma factor {sigma}B, encoded by sigB, is responsible for regulating transcription of several L. monocytogenes virulence and stress-response genes, including genes that contribute to establishment of gastrointestinal infections. A quantitative RT-PCR assay was used to measure mRNA transcript accumulation for the virulence genes inlA and bsh, the stress-response genes opuCA and lmo0669 (encoding a carnitine transporter and an oxidoreductase, respectively) and the housekeeping gene rpoB. Assays were conducted on mid-exponential phase L. monocytogenes cells exposed to conditions reflecting osmotic (0·3 M NaCl) or acid (pH 4·5) conditions typical for the human intestinal lumen. In exponential-phase cells, as well as under osmotic and acid stress, inlA, opuCA and bsh showed significantly lower absolute expression levels in a L. monocytogenes {Delta}sigB null mutant compared to wild-type. A statistical model that normalized target gene expression relative to rpoB showed that accumulation of inlA, opuCA and bsh transcripts was significantly increased in the wild-type strain within 5 min of acid and osmotic stress exposure; lmo0669 transcript accumulation increased significantly only after acid exposure. It was concluded that {sigma}B is essential for rapid induction of the tested stress-response and virulence genes under conditions typically encountered during gastrointestinal passage. As inlA, bsh and opuCA are critical for gastrointestinal infections in animal models, the data also suggest that {sigma}B contributes to the ability of L. monocytogenes to cause foodborne infections.


Abbreviations: qRT-PCR, quantitative RT-PCR




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