Publication:
A natural Vibrio parahaemolyticus ΔpirAVp pirBVp+ mutant kills shrimp but produces neither PirVp toxins nor acute hepatopancreatic necrosis disease lesions

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.date.issuedBE2560
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.format.mimetypeapplication/pdf
dc.identifier.citationApplied and Environmental Microbiology. Vol 83, No.16 (2017), p.-
dc.identifier.doi10.1128/AEM.00680-17
dc.identifier.issn992240
dc.identifier.other2-s2.0-85026555961
dc.identifier.urihttps://hdl.handle.net/20.500.14740/4115
dc.rights.holderScopus
dc.subject.otherDNA
dc.subject.otherElectrophoresis
dc.subject.otherMetabolites
dc.subject.otherShellfish
dc.subject.otherToxic materials
dc.subject.otherTranscription
dc.subject.otherAHPND
dc.subject.otherPenaeus vannamei
dc.subject.otherPir toxin
dc.subject.otherShrimp
dc.subject.otherVibrio parahaemolyticus
dc.subject.otherGenes
dc.subject.otherBacterial disease
dc.subject.otherBacterium
dc.subject.otherCells and cell components
dc.subject.otherCrustacean
dc.subject.otherDisease incidence
dc.subject.otherGene
dc.subject.otherGene expression
dc.subject.otherGenetic analysis
dc.subject.otherMortality
dc.subject.otherPlasmid
dc.subject.otherProtein
dc.subject.otherRNA
dc.subject.otherStomach content
dc.subject.otherToxin
dc.subject.otherVirulence
dc.subject.otherDecapoda (Crustacea)
dc.subject.otherLitopenaeus vannamei
dc.subject.otherVibrio parahaemolyticus
dc.titleA natural Vibrio parahaemolyticus ΔpirAVp pirBVp+ mutant kills shrimp but produces neither PirVp toxins nor acute hepatopancreatic necrosis disease lesions
dc.typeArticle
dspace.entity.typePublication
swu.datasource.scopushttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85026555961&doi=10.1128%2fAEM.00680-17&partnerID=40&md5=83b7ab0784042dd99562fad8335eef92

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