Serological detection of Grapevine leafroll virus 2 using an antiserum developed against the recombinant coat protein

  • Ling K
  • Zhu H
  • Petrovic N
 et al. 
  • 14


    Mendeley users who have this article in their library.
  • 17


    Citations of this article.


Grapevine leafroll associated virus 2 (GLRaV 2) is one of the important components in the leafroll disease complex. The coat protein gene of GLRaV 2 was cloned into a protein expression vector pMAL-c2x and the recombinant protein, consisting of the maltose binding protein (MBP) and GLRaV 2 coat protein (CP), was expressed in Escherichia coli. The recombinant MBP-CP was used to raise a high quality antiserum. When used in Western blot analysis, the anti-MBP-CP antiserum produced specific reaction to the recombinant protein as well as to the viral coat protein of GLRaV 2. In Immunosorbent electron microscopy study, the anti-MBP-CP antibodies strongly decorated the GLRaV 2 virions. Using the newly developed antiserum, an indirect plate-trapped antigen enzyme-linked immunosorbent assay method was developed and successfully implemented for virus detection. A field survey was conducted to evaluate the virus infection status by GLRaV 2 and GLRaV 3 using antibodies developed against their respective recombinant coat proteins.

Author-supplied keywords

  • Closterovirus
  • Electron microscopy
  • Vitis vinifera
  • Western blot

Get free article suggestions today

Mendeley saves you time finding and organizing research

Sign up here
Already have an account ?Sign in

Find this document

Get full text


  • K. S. Ling

  • H. Y. Zhu

  • N. Petrovic

  • D. Gonsalves

Cite this document

Choose a citation style from the tabs below

Save time finding and organizing research with Mendeley

Sign up for free