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Advisor(s)
Abstract(s)
Testing for Grapevine leafroll-associated virus 1 (GLRaV-1) is mandatory in certification schemes of propagation
material within the EU. Accurate and reliable diagnostic assays are necessary for implementation
of this measure. During routine detection of GLRaV-1, using double antibody sandwich enzyme-linked
immunosorbent assay (DAS-ELISA) and reverse transcription (RT) followed by polymerase chain reaction
(PCR), evidence was obtained that positive samples could be overlooked by either or both detection
methods. With the aim of improving serological detection tools for GLRaV-1, a total of 20 isolates were
analyzed and 83 new complete capsid protein (CP) gene sequences were obtained. This set, together with
the CP sequences available at GenBank was used for a comprehensive in silico analysis. To obtain a specific
antibody able to recognize all known CP variants, conserved regions with suitable antigenicity profile
were identified along the deduced CP AA sequences and a 14 AA sequence was chosen for commercial
peptide synthesis and immunization. Initially polyclonal antibodies were produced and tested, followed
by purification of the respective monospecific antibody and conjugation with alkaline phosphatase or
fluorescein isothiocyanate (FITC). These serological tools were tested successfully on all the available
positive samples and proved adequate for in situ immunoassay (ISIA). Further testing showed that the
monospecific antibody could also be used in tissue print immunoblotting (TPIB), a technique that allows
rapid processing of large sample sets, which is highly suitable to implement protocols ensuring that, for
each vine analyzed, enough random samples are taken and processed, before certification.
Description
Keywords
Antibodies Tissue print immunoblotting In situ immunoassay Capsid protein Intra-isolate genetic structure Molecular variability
Citation
Publisher
Elsevier