Publication: Multiplex RT-nested PCR differentiation of gill-associated virus (Australia) from yellow head virus (Thailand) of Penaeus monodon
Issued Date
2004-04-01
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ISSN
01660934
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2-s2.0-1442335321
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Mahidol University
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SCOPUS
Bibliographic Citation
Journal of Virological Methods. Vol.117, No.1 (2004), 49-59
Suggested Citation
Jeff A. Cowley, Lee C. Cadogan, Chainarong Wongteerasupaya, R. A J Hodgson, Vichai Boonsaeng, Peter J. Walker Multiplex RT-nested PCR differentiation of gill-associated virus (Australia) from yellow head virus (Thailand) of Penaeus monodon. Journal of Virological Methods. Vol.117, No.1 (2004), 49-59. doi:10.1016/j.jviromet.2003.11.018 Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/21392
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Title
Multiplex RT-nested PCR differentiation of gill-associated virus (Australia) from yellow head virus (Thailand) of Penaeus monodon
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Abstract
A multiplex RT-nested PCR has been developed to detect and differentiate the closely related prawn viruses, gill-associated virus (GAV) from Australia and yellow head virus (YHV) from Thailand. RT-PCR using primers to conserved sequences in the ORF1b gene amplified a 794bp region of either GAV or YHV. Nested PCR using a conserved sense primer and either a GAV- or YHV-specific antisense primer to a divergent sequence differentially amplified a 277bp region of the primary PCR amplicon. Multiplexing the YHV antisense primer with a GAV antisense primer to another divergent sequence allowed the viruses to be distinguished in a single nested PCR. Nested PCR enhanced detection sensitivity between 100- and 1000-fold and GAV or YHV RNA was detectable in ∼10fg lymphoid organ total RNA. The multiplex RT-nested PCR was also able to co-detect GAV and YHV RNA mixed over a wide range of concentrations to simulate potential dual-infection states. The robustness of the test was examined using RNA samples from Penaeus monodon prawns infected either chronically or acutely with GAV or YHV and collected at different locations in Eastern Australia and Thailand between 1994 and 1998. GAV- (406bp) or YHV-specific (277bp) amplicons were differentially generated in all cases, including five YHV RNA samples in which no primary RT-PCR amplicon was detected. Sequence analysis of GAV and YHV PCR amplicons identified minor variations in the regions targeted by the virus-specific antisense primers. However, none occurred at positions that critically affected the PCR. Crown Copyright © 2003 Published by Elsevier B.V. All rights reserved.