[[[ Aim: ]]] In vivo induced genes are thought to play an important role during infection of host. AlkA was identified as an in vivo-induced gene by in vivo expression technology (IVET), but its virulence in Shigella flexneri was not reported. The purpose of this study was to identify the role of alkA gene in the pathogenesis of S. flexneri. [[[ Methods: ]]] PCR was used to amplify alkA gene of S. flexneri 2a and fragment 028pKm. The fragment was then transformed into 2457T05 strain, a S flexneri 2a strain containing Red recombination system, which was constructed with a recombinant suicide plasmid pXLkd46. By in vivo homologous recombination, alkA mutants were obtained and verified by PCR and sequencing. Intracellular survival assay and virulence assay were used to test the intracellular survival ability in HeLa cell model and the virulence in mice lung infection model respectively. [[[ Results: ]]] Deletion mutant of S. flexneri 2a alkA was successfully constructed by gamma Red recombination system. The mutant exhibited significant survival defects and much significant virulence defects in mice infection assay. [[[ Conclusion: ]]] AlkA gene plays an important role in the infection of epithelial cells and is a virulent gene of Shigella spp.
Identification ofalkAgene related to virulence ofShigella flexneri 2aby mutational analysis
Shigella flexneri 2a의 병원성과 관련된 alkA 유전자의 식별을 위한 돌연변이 분석
[Category] 세균성이질,
[Article Type] journal-article
[Source] pubmed
All Keywords