Detecting bluetongue virus RNA in cell culture by dot hybridization with a cloned genetic probe

K. R.E. Squire, R. Y. Chuang, L. F. Chuang, R. H. Doi, Bennie Osburn

Research output: Contribution to journalArticle

11 Citations (Scopus)

Abstract

A 70% copy of genome segment 7 of bluetongue virus (BTV)-17 has been cloned into the plasmid pBR-322. This cloned BTV segment when used as a radioactive probe will hybridize to BTV doublestranded RNA extracted from cell cultures and dotted onto nitrocellulose paper. This dot hybridization technique is therefore suitable for detecting and identifying BTV in cell culture. The specificity of cloned probes is discussed in relation to detecting gene sequences specific for either the bluetongue serogroup or different serotypes of BTV.

Original languageEnglish (US)
Pages (from-to)59-68
Number of pages10
JournalJournal of Virological Methods
Volume10
Issue number1
DOIs
StatePublished - Jan 1 1985

Fingerprint

Bluetongue virus
Cell Culture Techniques
RNA
Bluetongue
Collodion
Plasmids
Genome
Genes

Keywords

  • bluetongue virus detection
  • dot hybridization
  • molecular cloning

ASJC Scopus subject areas

  • Virology

Cite this

Detecting bluetongue virus RNA in cell culture by dot hybridization with a cloned genetic probe. / Squire, K. R.E.; Chuang, R. Y.; Chuang, L. F.; Doi, R. H.; Osburn, Bennie.

In: Journal of Virological Methods, Vol. 10, No. 1, 01.01.1985, p. 59-68.

Research output: Contribution to journalArticle

Squire, K. R.E. ; Chuang, R. Y. ; Chuang, L. F. ; Doi, R. H. ; Osburn, Bennie. / Detecting bluetongue virus RNA in cell culture by dot hybridization with a cloned genetic probe. In: Journal of Virological Methods. 1985 ; Vol. 10, No. 1. pp. 59-68.
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