Publication: Listeria monocytogenes 10403S Alternative Sigma-54 Factor σ<sup>L</sup> Has a Negative Role on Survival Ability Under Bile Exposure
Issued Date
2021-10-21
Resource Type
ISSN
1664302X
Other identifier(s)
2-s2.0-85118655546
Rights
Mahidol University
Rights Holder(s)
SCOPUS
Bibliographic Citation
Frontiers in Microbiology. Vol.12, (2021)
Suggested Citation
Atsadang Boonmee, Haley F. Oliver, Soraya Chaturongakul Listeria monocytogenes 10403S Alternative Sigma-54 Factor σ<sup>L</sup> Has a Negative Role on Survival Ability Under Bile Exposure. Frontiers in Microbiology. Vol.12, (2021). doi:10.3389/fmicb.2021.713383 Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/77204
Research Projects
Organizational Units
Authors
Journal Issue
Thesis
Title
Listeria monocytogenes 10403S Alternative Sigma-54 Factor σ<sup>L</sup> Has a Negative Role on Survival Ability Under Bile Exposure
Other Contributor(s)
Abstract
Listeria monocytogenes is a Gram-positive bacterium causing listeriosis in animals and humans. To initiate a foodborne infection, L. monocytogenes has to pass through the host gastrointestinal tract (GIT). In this study, we evaluated survival abilities of L. monocytogenes 10403S wild type (WT) and its isogenic mutants in alternative sigma (σ) factor genes (i.e., sigB, sigC, sigH, and sigL) under simulated gastric, duodenal, and bile fluids. Within 10min of exposures, only bile fluid was able to significantly reduce survival ability of L. monocytogenes WT by 2 logs CFU/ml. Loss of sigL showed the greatest bile resistance among 16 strains tested, p<0.0001, (i.e., WT, four single alternative σ factor mutants, six double mutants, four triple mutants, and one quadruple mutant). To further investigate the role of σL in bile response, RNA-seq was conducted to compare the transcriptional profiles among L. monocytogenes 10403S ΔBCH triple mutant (lacking sigB, sigC, and sigH genes; expressing housekeeping σA and σL) and ΔBCHL quadruple mutant (lacking all alternative sigma factor genes; expressing only σA) strains under BHI and 1% bile conditions. A total of 216 and 176 differentially expressed genes (DEGs) were identified in BHI and bile, respectively. We confirmed that mpt operon was shown to be strongly activated by σL. Interestingly, more than 80% of DEGs were found to be negatively regulated in the presence of σL. This includes PrfA regulon and its mediated genes (i.e., hly, hpt, inlB, clpP, clpE, groL, and inlC) which were downregulated in response to bile in the presence of σL. This result suggests the potential negative role of σL on bile survival, and the roles of σL and σB might be in a seesaw model prior to host cell invasion.
