Development of fluorescence quantitative PCR for detection of genogroup Ⅰ Sapporo-like viruses in shellfish
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Graphical Abstract
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Abstract
ObjectiveTo develop a fluorescence quantitative polymerase chain reaction(FQ-PCR)for the detection of geno group I(GI)Sapporo-like viruses(SLVs)in shellfish.MethodsSLVs were concentrated by PEG 6000.The degenerate primers and probe were designed following large scale SLVs genome consensus analysis and subsequently a FQ-PCR assay for detection of GISLVs was established.ResultsT the assay developed possessed high accuracy and repetition for SLVs detection.The sensitivity of the assay was as low as 102 copies per reaction.The assay was linear within 5-log dynamic range between 102 copies and 106 copies.The correlation coefficient of the standard curve was 0.9988.ConclusionThe detection method of geno group I Sapporo-like viruses was established with FQ-PCR and can be used for rapid detection of SLVs pollution in shellfish and emergency of SLVs.
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