Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/14002
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dc.contributor.authorChaivisuthangkura P.
dc.contributor.authorSenapin S.
dc.contributor.authorWangman P.
dc.contributor.authorLongyant S.
dc.contributor.authorSithigorngul P.
dc.date.accessioned2021-04-05T03:32:50Z-
dc.date.available2021-04-05T03:32:50Z-
dc.date.issued2013
dc.identifier.issn3048608
dc.identifier.other2-s2.0-84883295294
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/14002-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84883295294&doi=10.1007%2fs00705-013-1680-0&partnerID=40&md5=30268c0316338cc3f9d0c073131b38ed
dc.description.abstractA strip test was developed for detection of infectious myonecrosis virus (IMNV) using a pair of monoclonal antibodies (MAbs), called IMN7 and IMC6, that are specific for the N and C fragments, respectively, of the IMNV capsid protein. The test strips were placed in plastic cassettes and stored desiccated in sealed plastic bags. In detection assays using the test-strip cassettes, 100-μl samples of application buffer containing homogenates from muscles or pleopods of normal or IMNV-infected shrimp were applied to the cassette sample chamber. Subsequent flow through the glass-fiber pad and the nitrocellulose membrane strip led to the development of visible antibody-protein complexes within 15 min. In samples containing IMNV, viral capsid protein bound to gold-labeled IMN7 in the glass-fiber pad and the complex was subsequently captured by MAb IMC6 at the T line to form a reddish-purple band. Any unbound gold-labeled IMN7 migrated past the T line to be captured by the GAM antibody to form a band at the C line. Samples without IMNV or containing it below the test detection limit gave reddish-purple bands only at the C line. The sensitivity of the test was comparable to that of dot blot tests using single MAbs but was ~300-fold less sensitive than a one-step RT-PCR test for IMNV. Despite this lower sensitivity, the strip test has advantages of low cost, speed and simplicity (i.e., no sophisticated equipment or specialized skills required), and it is appropriate for use by farmers for pathogen confirmation when IMNV is suspected in diseased shrimp. © 2013 Springer-Verlag Wien.
dc.subjectcapsid protein
dc.subjectcolloidal gold
dc.subjectmonoclonal antibody
dc.subjectvirus antibody
dc.subjectanimal
dc.subjectarticle
dc.subjectchemistry
dc.subjectevaluation
dc.subjectgenetics
dc.subjectimmunoaffinity chromatography
dc.subjectimmunology
dc.subjectisolation and purification
dc.subjectmethodology
dc.subjectPenaeidae
dc.subjectreverse transcription polymerase chain reaction
dc.subjectRNA virus
dc.subjectsensitivity and specificity
dc.subjecttime
dc.subjectvirology
dc.subjectAnimals
dc.subjectAntibodies, Monoclonal
dc.subjectAntibodies, Viral
dc.subjectCapsid Proteins
dc.subjectGold Colloid
dc.subjectImmunochromatography
dc.subjectPenaeidae
dc.subjectReverse Transcriptase Polymerase Chain Reaction
dc.subjectRNA Viruses
dc.subjectSensitivity and Specificity
dc.subjectTime Factors
dc.subjectDecapoda (Crustacea)
dc.subjectMiridae
dc.titleSimple and rapid detection of infectious myonecrosis virus using an immunochromatographic strip test
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationArchives of Virology. Vol 158, No.9 (2013), p.1925-1930
dc.identifier.doi10.1007/s00705-013-1680-0
Appears in Collections:Scopus 1983-2021

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