Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/100529
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dc.titleEdwardsiella tarda mutants defective in siderophore production, motility, serum resistance and catalase activity
dc.contributor.authorMathew, J.A.
dc.contributor.authorTan, Y.P.
dc.contributor.authorSrinivasa Rao, P.S.
dc.contributor.authorLim, T.M.
dc.contributor.authorLeung, K.Y.
dc.date.accessioned2014-10-27T08:26:52Z
dc.date.available2014-10-27T08:26:52Z
dc.date.issued2001
dc.identifier.citationMathew, J.A.,Tan, Y.P.,Srinivasa Rao, P.S.,Lim, T.M.,Leung, K.Y. (2001). Edwardsiella tarda mutants defective in siderophore production, motility, serum resistance and catalase activity. Microbiology 147 (2) : 449-457. ScholarBank@NUS Repository.
dc.identifier.issn13500872
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/100529
dc.description.abstractEdwardsiella tarda is a Gram-negative bacterium that causes a systemic infection, edwardsiellosis, in fish. The virulence factors of this pathogen and its genetic determinants have not been systematically examined. In this study, TnphoA transposon mutagenesis was used to construct a library of 440 alkaline phosphatase (PhoA+) fusion mutants from a total of 400 000 transconjugants derived from Ed. tarda PPD130/91. This library included genes for secreted and membrane-associated proteins normally involved in virulence. The library was screened for four virulence factors: siderophore production, motility, serum resistance and catalase production. Eight mutants deficient in one or more of these phenotypes were grouped into four classes. They were further characterized for their stimulation of reactive oxygen intermediate production by fish phagocytes, for their adhesion to and internalization into EPC (epithelioma papillosum of carp) cells, and for attenuation of virulence in blue gourami. Mutants 2A and 34 were highly attenuated in fish, with LD50 values about 10 times higher than for the wild-type. These strains had mutations in the genes encoding arylsulfate sulfotransferase (mutant 2A) and a catalase precursor protein (mutant 34). One hyperinvasive/adhesive mutant and four pst mutants that were pleiotropic and slightly attenuated in fish were also isolated.
dc.sourceScopus
dc.subjectFish pathogen
dc.subjectTransposon mutagenesis
dc.subjectVirulence genes
dc.typeArticle
dc.contributor.departmentBIOLOGICAL SCIENCES
dc.description.sourcetitleMicrobiology
dc.description.volume147
dc.description.issue2
dc.description.page449-457
dc.description.codenMROBE
dc.identifier.isiutNOT_IN_WOS
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