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Applied and Environmental Microbiology, November 2008, p. 6848-6858, Vol. 74, No. 22
0099-2240/08/$08.00+0 doi:10.1128/AEM.00442-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.
Identification of Components of the Sigma B Regulon in Listeria monocytogenes That Contribute to Acid and Salt Tolerance 
F. Abram,1
E. Starr,1
K. A. G. Karatzas,1
K. Matlawska-Wasowska,1
A. Boyd,1
M. Wiedmann,2
K. J. Boor,2
D. Connally,1 and
C. P. O'Byrne1*
Department of Microbiology, National University of Ireland—Galway, Galway, Ireland,1 Department of Food Science, 412 Stocking Hall, Cornell University, Ithaca, New York 148532
Received 22 February 2008/ Accepted 10 September 2008
Sigma B (
B) is an alternative sigma factor that controls the transcriptional response to stress in Listeria monocytogenes and is also known to play a role in the virulence of this human pathogen. In the present study we investigated the impact of a sigB deletion on the proteome of L. monocytogenes grown in a chemically defined medium both in the presence and in the absence of osmotic stress (0.5 M NaCl). Two new phenotypes associated with the sigB deletion were identified using this medium. (i) Unexpectedly, the strain with the 
sigB deletion was found to grow faster than the parent strain in the growth medium, but only when 0.5 M NaCl was present. This phenomenon was independent of the carbon source provided in the medium. (ii) The sigB mutant was found to have unusual Gram staining properties compared to the parent, suggesting that B contributes to the maintenance of an intact cell wall. A proteomic analysis was performed by two-dimensional gel electrophoresis, using cells growing in the exponential and stationary phases. Overall, 11 proteins were found to be differentially expressed in the wild type and the sigB mutant; 10 of these proteins were expressed at lower levels in the mutant, and 1 was overexpressed in the mutant. All 11 proteins were identified by tandem mass spectrometry, and putative functions were assigned based on homology to proteins from other bacteria. Five proteins had putative functions related to carbon utilization (Lmo0539, Lmo0783, Lmo0913, Lmo1830, and Lmo2696), while three proteins were similar to proteins whose functions are unknown but that are known to be stress inducible (Lmo0796, Lmo2391, and Lmo2748). To gain further insight into the role of B in L. monocytogenes, we deleted the genes encoding four of the proteins, lmo0796, lmo0913, lmo2391, and lmo2748. Phenotypic characterization of the mutants revealed that Lmo2748 plays a role in osmotolerance, while Lmo0796, Lmo0913, and Lmo2391 were all implicated in acid stress tolerance to various degrees. Invasion assays performed with Caco-2 cells indicated that none of the four genes was required for mammalian cell invasion. Microscopic analysis suggested that loss of Lmo2748 might contribute to the cell wall defect observed in the sigB mutant. Overall, this study highlighted two new phenotypes associated with the loss of B. It also demonstrated clear roles for B in both osmotic and low-pH stress tolerance and identified specific components of the B regulon that contribute to the responses observed.
* Corresponding author. Mailing address: Department of Microbiology, National University of Ireland—Galway, Galway, Ireland. Phone: 35391512342. Fax: 35391494598. E-mail: conor.obyrne{at}nuigalway.ie
Published ahead of print on 19 September 2008.
Applied and Environmental Microbiology, November 2008, p. 6848-6858, Vol. 74, No. 22
0099-2240/08/$08.00+0 doi:10.1128/AEM.00442-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.
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