Publication:
Suppression of shrimp melanization during white spot syndrome virus infection

dc.contributor.authorJantiwan Sutthangkulen_US
dc.contributor.authorPiti Amparyupen_US
dc.contributor.authorWalaiporn Charoensapsrien_US
dc.contributor.authorSaengchan Senapinen_US
dc.contributor.authorKornsunee Phiwsaiyaen_US
dc.contributor.authorAnchalee Tassanakajonen_US
dc.contributor.otherChulalongkorn Universityen_US
dc.contributor.otherThailand National Center for Genetic Engineering and Biotechnologyen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-11-23T09:45:18Z
dc.date.available2018-11-23T09:45:18Z
dc.date.issued2015-03-06en_US
dc.description.abstract© 2015 by The American Society for Biochemistry and Molecular Biology, Inc. The melanization cascade, activated by the prophenoloxidase (proPO) system, plays a key role in the production of cytotoxic intermediates, as well as melanin products for microbial sequestration in invertebrates. Here, we show that the proPO system is an important component of the Penaeus monodon shrimp immune defense toward a major viral pathogen, white spot syndrome virus (WSSV). Gene silencing of PmproPO(s) resulted in increased cumulative shrimp mortality after WSSV infection, whereas incubation ofWSSVwith an in vitro melanization reaction prior to injection into shrimp significantly increased the shrimp survival rate. The hemolymph phenoloxidase (PO) activity of WSSV-infected shrimp was extremely reduced at days 2 and 3 post-injection compared with uninfected shrimp but was fully restored after the addition of exogenous trypsin, suggesting that WSSV probably inhibits the activity of some proteinases in the proPO cascade. Using yeast two-hybrid screening and co-immunoprecipitation assays, the viral protein WSSV453 was found to interact with the proPO-activating enzyme 2 (PmPPAE2) of P. monodon. Gene silencing of WSSV453 showed a significant increase of PO activity in WSSV-infected shrimp, whereas co-silencing of WSSV453 and PmPPAE2 did not, suggesting that silencing of WSSV453 partially restored the PO activity via PmPPAE2 in WSSV-infected shrimp. Moreover, the activation of PO activity in shrimp plasma by PmPPAE2 was significantly decreased by preincubation with recombinant WSSV453. These results suggest that the inhibition of the shrimp proPO system byWSSVpartly occurs via thePmPPAE2-inhibiting activity of WSSV453.en_US
dc.identifier.citationJournal of Biological Chemistry. Vol.290, No.10 (2015), 6470-6481en_US
dc.identifier.doi10.1074/jbc.M114.605568en_US
dc.identifier.issn1083351Xen_US
dc.identifier.issn00219258en_US
dc.identifier.other2-s2.0-84924891305en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/35488
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84924891305&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleSuppression of shrimp melanization during white spot syndrome virus infectionen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84924891305&origin=inwarden_US

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