Publication:
Infectious myonecrosis virus (IMNV) and Decapod iridescent virus 1 (DIV1) detected in captured, wild Penaeus monodon

dc.contributor.authorJiraporn Srisalaen_US
dc.contributor.authorPiyachat Sanguanruten_US
dc.contributor.authorDararat Thaiueen_US
dc.contributor.authorSaensook Laiphromen_US
dc.contributor.authorJittima Siriwattanoen_US
dc.contributor.authorJuthatip Khudeten_US
dc.contributor.authorSorawit Powtongsooken_US
dc.contributor.authorTimothy W. Flegelen_US
dc.contributor.authorKallaya Sritunyalucksanaen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherThailand National Center for Genetic Engineering and Biotechnologyen_US
dc.contributor.otherIntegrative Aquaculture Biotechnology Research Groupen_US
dc.date.accessioned2022-08-04T07:54:03Z
dc.date.available2022-08-04T07:54:03Z
dc.date.issued2021-12-15en_US
dc.description.abstractInfectious myonecrosis virus (IMNV) was first discovered in the Americas in 2004 as a new lethal pathogen of cultivated whiteleg shrimp Penaeus vannamei, but infections were not lethal for the giant tiger shrimp Penaeus monodon. In 2007, it was reported in diseased P. vannamei cultivated in Indonesia but, until recently, not from other countries in Asia. Decapod iridescent virus (DIV1) was first reported from China in 2016 and is lethal for the crayfish Cherax quadricarinatus and Procambarus clarkii, for the penaeid shrimp P. vannamei and for the palaemonid shrimp Macrobrachium rosenbergii and Exopalaemon carinicauda. It has not yet been reported from other Asian countries. Here we describe the occurrence of positive test results for IMNV and DIV1 using polymerase chain reaction (PCR) technology during screening of grossly normal, broodstock-size, wild P. monodon captured and held in a biosecurity facility for screening. Amplicons for each virus were obtained from two widely separated targets in the relevant viral genomes listed at GenBank, and sequencing revealed 99–100% identity to the targets for each virus. Due to the positive results, the captured specimens were immediately destroyed within the quarantine facility. The results raised the possibility that grossly normal, captured P. monodon might serve as potential vehicles for introduction of IMNV and/or DIV1 to shrimp hatcheries and farms. Thus, we recommend that appropriate precautions be taken and that surveillance programs for farmed and wild populations be undertaken to avoid this possibility.en_US
dc.identifier.citationAquaculture. Vol.545, (2021)en_US
dc.identifier.doi10.1016/j.aquaculture.2021.737262en_US
dc.identifier.issn00448486en_US
dc.identifier.other2-s2.0-85112395183en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/75508
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85112395183&origin=inwarden_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.titleInfectious myonecrosis virus (IMNV) and Decapod iridescent virus 1 (DIV1) detected in captured, wild Penaeus monodonen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85112395183&origin=inwarden_US

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