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Simultaneous and rapid detection of white spot syndrome virus and yellow head virus infection in shrimp with a dual immunochromatographic strip test

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dc.contributor.author Sithigorngul P.
dc.contributor.author Rukpratanporn S.
dc.contributor.author Chaivisuthangkura P.
dc.contributor.author Sridulyakul P.
dc.contributor.author Longyant S.
dc.date.accessioned 2021-04-05T03:35:32Z
dc.date.available 2021-04-05T03:35:32Z
dc.date.issued 2011
dc.identifier.issn 1660934
dc.identifier.other 2-s2.0-79952183202
dc.identifier.uri https://ir.swu.ac.th/jspui/handle/123456789/14546
dc.identifier.uri https://www.scopus.com/inward/record.uri?eid=2-s2.0-79952183202&doi=10.1016%2fj.jviromet.2011.01.011&partnerID=40&md5=afe5ff2b382da9400bee725b98b50fd6
dc.description.abstract A strip test for the dual detection of white spot syndrome virus (WSSV) and yellow head virus (YHV) was developed using monoclonal antibodies (MAbs) specific to the WSSV major envelope protein VP28 (W1 and W30) and the YHV nucleocapsid protein p20 (Y19 and Y21). The MAbs W30 and Y19 were conjugated with colloidal gold and sprayed onto a glass fiber pad that was placed adjacent to a sample chamber. The MAbs W1 and Y21 and the goat anti-mouse immunoglobulin G (GAM) antibody were sprayed onto a nitrocellulose membrane in strips at positions designated W, Y and C, respectively. These test strips were placed in plastic cases and stored desiccated in a plastic bag. The test strips were assessed for their ability to detect WSSV and YHV simultaneously using pleopods sampled from shrimp. A pleopod homogenate in application buffer 100μl was applied to the sample chamber to flow through the nitrocellulose membrane strip, and antibody-protein complexes could be observed within 15. min. In sample from shrimp infected with WSSV and/or YHV, viral protein bound to the colloidal gold-conjugated MAbs. These complexes were captured by the MAbs at the W and/or Y test lines, resulting in the appearance of reddish-purple coloured bands. Any unbound colloidal gold-conjugated MAbs migrated pass the W and Y lines would be captured by the GAM antibody, forming a band at position C. When samples not containing WSSV and YHV proteins or containing viral proteins at below the detection limit of the test, only the band at position C was observed. The sensitivity of the test was comparable to dot blot tests using single MAbs, and ~500-fold less sensitive than a 1-step PCR test for WSSV and 1000-fold less sensitive than an RT-PCR test for YHV. Despite this lower sensitivity, the dual strip test has advantages in speed and simplicity in not requiring sophisticated equipment or specialized skills. The ability to co-detect WSSV and YHV provides simultaneously cost savings. © 2011 Elsevier B.V.
dc.subject monoclonal antibody
dc.subject virus protein
dc.subject animal experiment
dc.subject article
dc.subject controlled study
dc.subject diagnostic test accuracy study
dc.subject ichthyophthiriasis
dc.subject immunoassay
dc.subject immunochromatographic strip test
dc.subject intermethod comparison
dc.subject nonhuman
dc.subject priority journal
dc.subject reverse transcription polymerase chain reaction
dc.subject RNA virus
dc.subject RNA virus infection
dc.subject sensitivity and specificity
dc.subject shrimp
dc.subject test strip
dc.subject virus detection
dc.subject White spot syndrome virus
dc.subject Yellow head virus
dc.subject Yellow head virus infection
dc.subject Animals
dc.subject Antibodies, Monoclonal
dc.subject Antibodies, Viral
dc.subject Immunoassay
dc.subject Penaeidae
dc.subject Roniviridae
dc.subject Sensitivity and Specificity
dc.subject Virology
dc.subject White spot syndrome virus 1
dc.subject Capra hircus
dc.subject Decapoda (Crustacea)
dc.subject Litopenaeus vannamei
dc.subject Shrimp white spot syndrome virus
dc.subject Yellow head virus
dc.title Simultaneous and rapid detection of white spot syndrome virus and yellow head virus infection in shrimp with a dual immunochromatographic strip test
dc.type Article
dc.rights.holder Scopus
dc.identifier.bibliograpycitation Journal of Virological Methods. Vol 173, No.1 (2011), p.85-91
dc.identifier.doi 10.1016/j.jviromet.2011.01.011


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