Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/15240
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dc.contributor.authorSukhumsirichart W.
dc.contributor.authorKiatpathomchai W.
dc.contributor.authorWongteerasupaya C.
dc.contributor.authorWithyachumnarnkul B.
dc.contributor.authorFlegel T.W.
dc.contributor.authorBoonseang V.
dc.contributor.authorPanyim S.
dc.date.accessioned2021-04-05T04:33:09Z-
dc.date.available2021-04-05T04:33:09Z-
dc.date.issued2002
dc.identifier.issn8908508
dc.identifier.other2-s2.0-0036917189
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/15240-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-0036917189&doi=10.1006%2fmcpr.2002.0435&partnerID=40&md5=b6fe1cd0deae94d040574a8a9a8d5f72
dc.description.abstractA rapid and sensitive PCR-ELISA has been developed for detection of hepatopancreatic parvovirus (HPV) in Penaeus monodon. The specific primer set amplified 156 bp fragment and could detect as a little as 0.01 fg of purified HPV DNA which equivalent to three viral particles. No cross-reactivity was observed when nucleic acid templates from white spot syndromevirus, yellow-head virus, monodon baculovirus and shrimp were tested. The crude DNA simple prepared from hepatopancreas can be used as DNA template and provide a favorable result. Using this technique for detection of HPV infection in 87 carrier shrimps revealed the higher sensitivity and efficiency of detection when compared to histological examination and conventional PCR. Sixty-two percent infection was detected by PCR-ELISA from samples with HPV negative diagnosed by histological examination. Therefore, this sensitive and specific method is promisingly useful for early detection of HPV infection in broodstock, carriers and for ex situ application where large numbers of samples can be analyzed simultaneously. © 2002 Published by Elsevier Science Ltd.
dc.subjectanimal tissue
dc.subjectarticle
dc.subjectcontrolled study
dc.subjectcross reaction
dc.subjectdiagnostic accuracy
dc.subjectDNA determination
dc.subjectearly diagnosis
dc.subjectenzyme linked immunosorbent assay
dc.subjectgene amplification
dc.subjecthepatopancreas
dc.subjecthistopathology
dc.subjectnonhuman
dc.subjectParvovirus
dc.subjectpolymerase chain reaction
dc.subjectpriority journal
dc.subjectsensitivity and specificity
dc.subjectshrimp
dc.subjectvirus detection
dc.subjectvirus infection
dc.subjectDecapoda (Crustacea)
dc.subjectHepatopancreatic parvovirus of penaeid shrimp
dc.subjectMonodon
dc.subjectMonodon baculovirus
dc.subjectParvovirus
dc.subjectPenaeus monodon
dc.subjectunidentified baculovirus
dc.subjectYellow head virus
dc.titleDetection of hepatopancreatic parvovirus (HPV) infection in Penaeus monodon using PCR-ELISA
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationMolecular and Cellular Probes. Vol 16, No.6 (2002), p.409-413
dc.identifier.doi10.1006/mcpr.2002.0435
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