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Real-time PCR assay for specific detection of cowpox virus.

Authors :
Maksyutov, Rinat A.
Gavrilova, Elena V.
Meyer, Hermann
Shchelkunov, Sergei N.
Source :
Journal of Virological Methods. Jan2015, Vol. 211, p8-11. 4p.
Publication Year :
2015

Abstract

The species cowpox virus (CPXV), genus Orthopoxvirus (OPV), consists of isolates highly variable in their biological properties and their genotypes. A TaqMan PCR assay for the specific detection of CPXV DNA based on sequences of the ORF D11L has been developed recently. ( Gavrilova et al . , 2010; Shchelkunov et al . , 2011 ); however, a rather limited panel of CPXV stains has been used. When a much larger panel of 47 CPXV DNAs has been tested, three strains could not be amplified at all because of large deletions in their respective ORF D11L. In addition, a deletion of 23 bp led to low-efficiency detection of five other CPXV strains. To solve this problem a new primer/probe combinations was selected based on sequences of ORF D8L, and a new real-time PCR method for (i) a genus-specific detection of OPVs and (ii) a simultaneous CPXV-specific differentiation is described in this study. The specificity and sensitivity were assessed by analyzing DNA of 67 strains belonging to human-pathogenic OPV species, including variola virus, as well as specimens of CPXV-infected mice. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01660934
Volume :
211
Database :
Academic Search Index
Journal :
Journal of Virological Methods
Publication Type :
Academic Journal
Accession number :
99827172
Full Text :
https://doi.org/10.1016/j.jviromet.2014.10.004