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Identification of alkA gene related to virulence of Shigella flexneri 2a by mutational analysis

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 th...

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Published in:World journal of gastroenterology : WJG 2003-12, Vol.9 (12), p.2720-2725
Main Authors: Shi, Zhao-Xing, Wang, Heng-Liang, Hu, Kun, Feng, Er-Ling, Yao, Xiao, Su, Guo-Fu, Huang, Pei-Tang, Huang, Liu-Yu
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container_title World journal of gastroenterology : WJG
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creator Shi, Zhao-Xing
Wang, Heng-Liang
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description 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. 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. 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. AlkA gene plays an important role in the infection of epithelial cells and is a virulent gene of Shigella spp.
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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. 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. 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. 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subjects Animals
Base Sequence
Basic Research
Binding Sites
Conjugation, Genetic
Disease Models, Animal
DNA Mutational Analysis
DNA Primers
Dysentery, Bacillary - microbiology
Gene Expression Regulation, Bacterial
Gene Expression Regulation, Enzymologic
Mice
NADH, NADPH Oxidoreductases - genetics
Polymerase Chain Reaction
Promoter Regions, Genetic - genetics
Shigella flexneri - classification
Shigella flexneri - enzymology
Shigella flexneri - genetics
Shigella flexneri - pathogenicity
Species Specificity
Virulence - genetics
title Identification of alkA gene related to virulence of Shigella flexneri 2a by mutational analysis
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