Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/14849
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dc.contributor.authorKhawsak P.
dc.contributor.authorDeesukon W.
dc.contributor.authorChaivisuthangkura P.
dc.contributor.authorSukhumsirichart W.
dc.date.accessioned2021-04-05T04:31:58Z-
dc.date.available2021-04-05T04:31:58Z-
dc.date.issued2008
dc.identifier.issn8908508
dc.identifier.other2-s2.0-42649113419
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/14849-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-42649113419&doi=10.1016%2fj.mcp.2007.12.005&partnerID=40&md5=62f58875842039b61a4627decd644e2e
dc.description.abstractIn the present study, multiplex reverse transcription-polymerase chain reaction (mRT-PCR) was developed for simultaneously detection of six major shrimp viruses including yellow-head virus (YHV), white spot syndrome virus (WSSV), Taura syndrome virus (TSV), hepatopancreatic parvovirus (HPV), infectious hypodermal and hematopoietic necrosis virus (IHHNV) and monodon baculovirus (MBV). The six primer sets could amplify viral nucleic acids resulting in PCR products with different sizes. They were highly specific and did not cross-hybridize with other viral or shrimp nucleic acids. The sensitivity of the multiplex RT-PCR was 0.15 pg for IHHNV, 0.15 pg for TSV, 1.00 pg for HPV, 1.5 pg for MBV, 5.00 pg for WSSV and 10.00 pg for YHV. In the field application, 42 samples including whole tissue of post-larvae and hepatopancreas of Penaeus monodon collected from ponds in the central and southern parts of Thailand during 2002-2005 were examined by multiplex RT-PCR. The results revealed that a single infection was dominant and WSSV was the highest prevalence at that time. Dual infection was found in one sample. This developed multiplex RT-PCR will be useful for simultaneous detection of six major viruses of penaeid shrimp and benefit to shrimp cultured industry. © 2008 Elsevier Ltd. All rights reserved.
dc.subjectaquaculture
dc.subjectarticle
dc.subjectcross hybridization
dc.subjectgene amplification
dc.subjecthepatopancreatic parvovirus
dc.subjectinfectious hypodermal and hematopoietic necrosis virus
dc.subjectlarva
dc.subjectmonodon baculovirus
dc.subjectnonhuman
dc.subjectnucleic acid analysis
dc.subjectnucleotide sequence
dc.subjectoligonucleotide probe
dc.subjectPenaeidae
dc.subjectprevalence
dc.subjectpriority journal
dc.subjectreverse transcription polymerase chain reaction
dc.subjectshrimp
dc.subjectTaura syndrome virus
dc.subjectThailand
dc.subjectvirus detection
dc.subjectvirus infection
dc.subjectvirus strain
dc.subjectWhite spot syndrome virus
dc.subjectyellow head virus
dc.subjectAnimals
dc.subjectDNA Primers
dc.subjectDNA Viruses
dc.subjectPenaeidae
dc.subjectReverse Transcriptase Polymerase Chain Reaction
dc.subjectRNA Viruses
dc.subjectRNA, Ribosomal
dc.subjectSensitivity and Specificity
dc.subjectDecapoda (Crustacea)
dc.subjectHepatopancreatic parvovirus of penaeid shrimp
dc.subjectHuman papillomavirus
dc.subjectInfectious hypodermal and hematopoietic necrosis virus
dc.subjectMonodon baculovirus
dc.subjectMushroom bacilliform virus
dc.subjectPenaeidae
dc.subjectPenaeus monodon
dc.subjectShrimp white spot syndrome virus
dc.subjectTaura syndrome virus
dc.subjectYellow head virus
dc.titleMultiplex RT-PCR assay for simultaneous detection of six viruses of penaeid shrimp
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationMolecular and Cellular Probes. Vol 22, No.3 (2008), p.177-183
dc.identifier.doi10.1016/j.mcp.2007.12.005
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