IDENTIFICATION OF A CDNA CLONE SPECIFIC TO GRAPEVINE LEAFROLL-ASSOCIATED VIRUS-1, AND OCCURRENCE OF THE VIRUS IN AUSTRALIA

Citation
N. Habili et al., IDENTIFICATION OF A CDNA CLONE SPECIFIC TO GRAPEVINE LEAFROLL-ASSOCIATED VIRUS-1, AND OCCURRENCE OF THE VIRUS IN AUSTRALIA, Plant Pathology, 46(4), 1997, pp. 516-522
Citations number
24
Categorie Soggetti
Plant Sciences",Agriculture
Journal title
ISSN journal
00320862
Volume
46
Issue
4
Year of publication
1997
Pages
516 - 522
Database
ISI
SICI code
0032-0862(1997)46:4<516:IOACCS>2.0.ZU;2-Z
Abstract
A cDNA clone derived from a leafroll infected low-yielding clone of Su ltana grapevine (syn. Thompson Seedless, Sultanina) hybridized specifi cally to dsRNA from a number of grapevine varieties that reacted with grapevine leafroll-associated virus 1 (GLRaV-1) antibody. The cDNA was sequenced, and a set of specific primers was designed and used in a s imple RT-PCR test using extracts from a range of grapevine varieties. The same vines were also tested by Western blotting or ELISA to assess the presence of GLRaV-1 coat protein. In every sample tested, the res ults of PCR tests were consistent with those of Western blots and ELIS A, indicating that the cDNA clone was specific to GLRaV-1. The occurre nce of GLRaV-1 strongly correlated with the low-yielding character of Sultana clones tested, suggesting that the virus may contribute to low yields in some leafroll-infected Sultana clones. The optimum time for detecting GLRaV-1 was determined to be early in summer. The DNA-based detection procedure reported here provides an alternative to detectio n by serology.