Publication: Infectious myonecrosis virus (IMNV) and Decapod iridescent virus 1 (DIV1) detected in captured, wild Penaeus monodon
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Issued Date
2021-12-15
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ISSN
00448486
Other identifier(s)
2-s2.0-85112395183
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Mahidol University
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SCOPUS
Bibliographic Citation
Aquaculture. Vol.545, (2021)
Suggested Citation
Jiraporn Srisala, Piyachat Sanguanrut, Dararat Thaiue, Saensook Laiphrom, Jittima Siriwattano, Juthatip Khudet, Sorawit Powtongsook, Timothy W. Flegel, Kallaya Sritunyalucksana Infectious myonecrosis virus (IMNV) and Decapod iridescent virus 1 (DIV1) detected in captured, wild Penaeus monodon. Aquaculture. Vol.545, (2021). doi:10.1016/j.aquaculture.2021.737262 Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/75508
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Title
Infectious myonecrosis virus (IMNV) and Decapod iridescent virus 1 (DIV1) detected in captured, wild Penaeus monodon
Abstract
Infectious 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.