Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/13052
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dc.contributor.authorPhiwsaiya K.
dc.contributor.authorCharoensapsri W.
dc.contributor.authorTaengphu S.
dc.contributor.authorDong H.T.
dc.contributor.authorSangsuriya P.
dc.contributor.authorNguyen G.T.T.
dc.contributor.authorPham H.Q.
dc.contributor.authorAmparyup P.
dc.contributor.authorSritunyalucksana K.
dc.contributor.authorTaengchaiyaphum S.
dc.contributor.authorChaivisuthangkura P.
dc.contributor.authorLongyant S.
dc.contributor.authorSithigorngul P.
dc.contributor.authorSenapin S.
dc.date.accessioned2021-04-05T03:22:09Z-
dc.date.available2021-04-05T03:22:09Z-
dc.date.issued2017
dc.identifier.issn992240
dc.identifier.other2-s2.0-85026555961
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/13052-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85026555961&doi=10.1128%2fAEM.00680-17&partnerID=40&md5=83b7ab0784042dd99562fad8335eef92
dc.description.abstractAcute hepatopancreatic necrosis disease (AHPND) of shrimp is caused by Vibrio parahaemolyticus isolates (VPAHPND isolates) that harbor a pVA plasmid encoding toxins PirAVp and PirBVp. These are released from VPAHPND isolates that colonize the shrimp stomach and produce pathognomonic AHPND lesions (massive sloughing of hepatopancreatic tubule epithelial cells). PCR results indicated that V. parahaemolyticus isolate XN87 lacked pirAVp but carried pirBVp. Unexpectedly, Western blot analysis of proteins from the culture broth of XN87 revealed the absence of both toxins, and the lack of PirBVp was further confirmed by enzyme-linked immunosorbent assay. However, shrimp immersion challenge with XN87 resulted in 47% mortality without AHPND lesions. Instead, lesions consisted of collapsed hepatopancreatic tubule epithelia. In contrast, control shrimp challenged with typical VPAHPND isolate 5HP gave 90% mortality, accompanied by AHPND lesions. Sequence analysis revealed that the pVA plasmid of XN87 contained a mutated pirAVp gene interrupted by the out-of-frame insertion of a transposon gene fragment. The upstream region and the beginning of the original pirAVp gene remained intact, but the insertion caused a 2-base reading frameshift in the remainder of the pirAVp gene sequence and in the downstream pirBVp gene sequence. Reverse transcription-PCR and sequencing of 5HP revealed a bicistronic pirABVp mRNA transcript that was not produced by XN87, explaining the absence of both toxins in its culture broth. However, the virulence of XN87 revealed that some V. parahaemolyticus isolates carrying mutant pVA plasmids that produce no PirVp toxins can cause mortality in shrimp in ponds experiencing an outbreak of early mortality syndrome (EMS) but may not have been previously recognized to be AHPND related because they did not cause pathognomonic AHPND lesions. © 2017 American Society for Microbiology.
dc.subjectDNA
dc.subjectElectrophoresis
dc.subjectMetabolites
dc.subjectShellfish
dc.subjectToxic materials
dc.subjectTranscription
dc.subjectAHPND
dc.subjectPenaeus vannamei
dc.subjectPir toxin
dc.subjectShrimp
dc.subjectVibrio parahaemolyticus
dc.subjectGenes
dc.subjectbacterial disease
dc.subjectbacterium
dc.subjectcells and cell components
dc.subjectcrustacean
dc.subjectdisease incidence
dc.subjectgene
dc.subjectgene expression
dc.subjectgenetic analysis
dc.subjectmortality
dc.subjectplasmid
dc.subjectprotein
dc.subjectRNA
dc.subjectstomach content
dc.subjecttoxin
dc.subjectvirulence
dc.subjectDecapoda (Crustacea)
dc.subjectLitopenaeus vannamei
dc.subjectVibrio parahaemolyticus
dc.titleA natural Vibrio parahaemolyticus ΔpirAVp pirBVp+ mutant kills shrimp but produces neither PirVp toxins nor acute hepatopancreatic necrosis disease lesions
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationApplied and Environmental Microbiology. Vol 83, No.16 (2017), p.-
dc.identifier.doi10.1128/AEM.00680-17
Appears in Collections:Scopus 1983-2021

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