Comparative detection of a large population of grapevine viruses by TaqMan^® RT-qPCR and ELISA

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• 作者：Sé ; bastien Bruisson^a ; ^b ; Sylvain Lebel^a ; ^b ; Bernard Walter^a ; Laurent Prevotat^b ; Sam Seddas^b ; Paul Schellenbaum^a ; ^{paul.schellenbaum@uha.fr}
• 关键词：Vitis ; Serological detection ; Molecular detection ; Multiplex
• 刊名：Journal of Virological Methods
• 出版年：2017
• 出版时间：February 2017
• 年：2017
• 卷：240
• 期：Complete
• 页码：73-77
• 全文大小：828 K
• 卷排序：240

文摘

Grapevine (Vitis spp.) can be infected by numerous viruses that are often widespread and of great economic importance. Reliable detection methods are necessary for sanitary selection which is the only way to partly control grapevine virus diseases. Biological indexing and ELISA are currently the standard methods for screening propagation material, and PCR-methods are becoming increasingly popular. Due to the diversity of virus isolates, it is essential to verify that the tests allow the detection of the largest possible virus populations. We developed three quadruplex TaqMan® RT-qPCR assays for detecting nine different viruses that cause considerable damage in many vineyards world-wide. Each assay is designed to detect three viruses and the grapevine Actin as an internal control.A large population of grapevines from diverse cultivars and geographic location was tested for the presence of nine viruses: Arabis mosaic virus (ArMV), Grapevine fleck virus (GFkV), Grapevine fanleaf virus (GFLV), Grapevine leafroll-associated viruses (GLRaV-1, -2, -3), Grapevine rupestris stem pitting-associated virus (GRSPaV), Grapevine virus A (GVA), and Grapevine virus B (GVB). In general, identical results were obtained with multiplex TaqMan® RT-qPCR and ELISA although, in some cases, viruses could be detected by only one of the two techniques.