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Cited 9 time in webofscience Cited 10 time in scopus
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Development of an immunochromatography assay kit for rapid detection of ranavirus

Authors
Kim, Young RimPark, Seong BinFagutao, Fernand F.Nho, Seong WonJang, Ho BinCha, In SeokThompson, Kim D.Adams, AlexandraBayley, AmandaJung, Tae Sung
Issue Date
Oct-2015
Publisher
ELSEVIER SCIENCE BV
Keywords
Detection kit; Frog; Ranavirus; Monoclonal antibodies; Colloidal gold-immunochromatography assay (GICA)
Citation
Journal of Virological Methods, v.223, pp 33 - 39
Pages
7
Indexed
SCI
SCIE
SCOPUS
Journal Title
Journal of Virological Methods
Volume
223
Start Page
33
End Page
39
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/16986
DOI
10.1016/j.jviromet.2015.07.009
ISSN
0166-0934
1879-0984
Abstract
Ranaviruses are large, double-stranded DNA viruses of the family Iridoviridae and are known to be primary pathogens in frogs, fish and other amphibians. These viruses have been shown to be highly adaptable and have the ability to cross species barriers, making them a potent threat to global biodiversity. There is therefore, a need for rapid and efficient diagnostic methods to control the spread of these viruses. To address this, monoclonal antibodies (MAbs) were developed against ranavirus strain FV-3 (standard frog virus 3) to detect the major capsid protein and FV-3gorfl9R related hypothetical protein in both the FV-3 and KRV-1 (Korean ranavirus) strains. The antibodies were then applied on a colloidal gold-immunochromatographic assay (GICA) as a kit for the detection of ranaviruses. The kit was able to detect low concentrations of the virus (10(1) TCID50/ml) and showed analytical specificity when tested against other viral pathogens, including those belonging to the same family. It was possible to detect ranavirus in experimentally infected frogs within 30 min using the kit. The kit described here is expected to be a valuable and informative tool for on-site detection of ranavirus in frog. (C) 2015 Elsevier B.V. All rights reserved.
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