An assay for the detection of grapevine leafroll-associated virus 3 using a single-chain fragment variable antibody |
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Authors: | Laura?Cogotzi Annalisa?Giampetruzzi Greta?N?lke Martin?Orecchia Vito?Elicio Maria?Antonietta?Castellano Giovanni?P.?Martelli Rainer?Fischer Stefan?Schillberg Pasquale?Saldarelli |
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Affiliation: | (1) Institute of Plant Virology, CNR, Bari and Department of Plant Protection and Applied Microbiology, University of Bari, Via Amendola 165/A, 70126 Bari, Italy;(2) Institute for Molecular Biotechnology (Biology VII), RWTH Aachen, Worringerweg 1, 52074 Aachen, Germany;(3) Present address: GlaxoSmithKline, Gunnels Wood Road, Stevenage, Herts, SG1 2NY, UK;(4) Fraunhofer Institute for Molecular Biology and Applied Ecology IME, Forckenbeckstrasse 6, 52074 Aachen, Germany;(5) Agritest s.r.l, Valenzano, Bari, Italy |
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Abstract: | Grapevine leafroll-associated virus 3 (GLRaV-3) is a major pathogen of grapevine. A previously described single-chain fragment variable (scFv) antibody (scFvLR3), directed against the coat protein (CP) of GLRaV-3, was expressed in Escherichia coli and used to develop a diagnostic ELISA kit. The antibody was fused to the light chain constant domain of human immunoglobulin to create the bivalent reagent CL-LR3, which was purified from the periplasmic fraction, giving a yield of ~5 mg/l. The sensitivity of the reagent against recombinant GLRaV-3 CP was 0.1 ng. The sensitivity, specificity and durability of the reagent was similar to a commercial kit. The CL-LR3 showed a weak cross-reaction in immune electron microscopy assays to GLRaV-1 and -7, but not with the phylogenetically more distant GLRaV-2. A fully recombinant kit was developed with the inclusion of a recombinant GLRaV-3 CP expressed in bacteria, thus avoiding problems associated with virus propagation and purification. This system represents a rapid, simple, sensitive and standardized diagnostic protocol for GLRaV-3 detection. |
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