Preparation of polyclonal antibody against recombinant coat protein of Cucumber mosaic virus isolate B13

Cucumber mosaic virus (CMV) is one of widely-spread viruses of plants with the broadest host range encompassing over 1200 species. One major limiting factor for detection of the virus is unavailability of the virus-specific antibodies especially in developing countries. Recombinant DNA technology fa...

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Main Authors: Davoud Koolivand, Nemat Sokhandan Bashir, Afshin Rostami
Format: Article
Language:English
Published: University of Tarbiat Modares 2017-03-01
Series:Journal of Crop Protection
Subjects:
Online Access:http://jcp.modares.ac.ir/article-3-7649-en.html
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author Davoud Koolivand
Nemat Sokhandan Bashir
Afshin Rostami
author_facet Davoud Koolivand
Nemat Sokhandan Bashir
Afshin Rostami
author_sort Davoud Koolivand
collection DOAJ
description Cucumber mosaic virus (CMV) is one of widely-spread viruses of plants with the broadest host range encompassing over 1200 species. One major limiting factor for detection of the virus is unavailability of the virus-specific antibodies especially in developing countries. Recombinant DNA technology facilitates antibody preparation without requiring special equipment. In this study, coat protein (CP) gene cDNA of CMV was subcloned from pTZ57CMVCP into pET21a expression vector and transformed into Escherichia coli strain Rosetta. Expression of CMV CP was examined by sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) and its identity was confirmed by western blotting, dot blot immunobinding assay (DIBA) and enzyme- linked immunosorbent assay (ELISA) using anti- CMV antibody. The expressed protein was purified using T7•Tag affinity purification kit and used as antigen for raising polyclonal antibodies in two mice. The purified anti-CMV CP IgG and the conjugated IgG performed favourably in terms of specificity and sensitivity to detect both expressed CP (antigen) and CMV isolates in infected cucurbit plants using plate trapped antigen (PTA)- ELISA, double-antibody sandwich (DAS)-ELISA and western blotting. The prepared antibodies can be applied in serological and sero-molecular tests in studies on the virus and in screening of plants for the infection. This is the first report of preparation of antibodies against CP of an indigenous isolate of CMV.
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spelling doaj.art-cd22b5dab25a4a1c9468f583f59b4c622022-12-22T02:11:39ZengUniversity of Tarbiat ModaresJournal of Crop Protection2251-90412251-905X2017-03-01612534Preparation of polyclonal antibody against recombinant coat protein of Cucumber mosaic virus isolate B13Davoud Koolivand0Nemat Sokhandan Bashir1Afshin Rostami2 Department of Plant Protection, Faculty of Agriculture, University of Zanjan, Zanjan-Iran. Department of Plant Protection, Faculty of Agriculture, University of Tabriz, Tabriz, Iran. Department of Plant Protection, Faculty of Agriculture, University of Zanjan, Zanjan-Iran. Cucumber mosaic virus (CMV) is one of widely-spread viruses of plants with the broadest host range encompassing over 1200 species. One major limiting factor for detection of the virus is unavailability of the virus-specific antibodies especially in developing countries. Recombinant DNA technology facilitates antibody preparation without requiring special equipment. In this study, coat protein (CP) gene cDNA of CMV was subcloned from pTZ57CMVCP into pET21a expression vector and transformed into Escherichia coli strain Rosetta. Expression of CMV CP was examined by sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) and its identity was confirmed by western blotting, dot blot immunobinding assay (DIBA) and enzyme- linked immunosorbent assay (ELISA) using anti- CMV antibody. The expressed protein was purified using T7•Tag affinity purification kit and used as antigen for raising polyclonal antibodies in two mice. The purified anti-CMV CP IgG and the conjugated IgG performed favourably in terms of specificity and sensitivity to detect both expressed CP (antigen) and CMV isolates in infected cucurbit plants using plate trapped antigen (PTA)- ELISA, double-antibody sandwich (DAS)-ELISA and western blotting. The prepared antibodies can be applied in serological and sero-molecular tests in studies on the virus and in screening of plants for the infection. This is the first report of preparation of antibodies against CP of an indigenous isolate of CMV.http://jcp.modares.ac.ir/article-3-7649-en.htmlantibodycoat proteincucumber mosaic viruse. coliexpressionwestern blot
spellingShingle Davoud Koolivand
Nemat Sokhandan Bashir
Afshin Rostami
Preparation of polyclonal antibody against recombinant coat protein of Cucumber mosaic virus isolate B13
Journal of Crop Protection
antibody
coat protein
cucumber mosaic virus
e. coli
expression
western blot
title Preparation of polyclonal antibody against recombinant coat protein of Cucumber mosaic virus isolate B13
title_full Preparation of polyclonal antibody against recombinant coat protein of Cucumber mosaic virus isolate B13
title_fullStr Preparation of polyclonal antibody against recombinant coat protein of Cucumber mosaic virus isolate B13
title_full_unstemmed Preparation of polyclonal antibody against recombinant coat protein of Cucumber mosaic virus isolate B13
title_short Preparation of polyclonal antibody against recombinant coat protein of Cucumber mosaic virus isolate B13
title_sort preparation of polyclonal antibody against recombinant coat protein of cucumber mosaic virus isolate b13
topic antibody
coat protein
cucumber mosaic virus
e. coli
expression
western blot
url http://jcp.modares.ac.ir/article-3-7649-en.html
work_keys_str_mv AT davoudkoolivand preparationofpolyclonalantibodyagainstrecombinantcoatproteinofcucumbermosaicvirusisolateb13
AT nematsokhandanbashir preparationofpolyclonalantibodyagainstrecombinantcoatproteinofcucumbermosaicvirusisolateb13
AT afshinrostami preparationofpolyclonalantibodyagainstrecombinantcoatproteinofcucumbermosaicvirusisolateb13