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Failure to genotype herpes simplex virus by real-time PCR assay and melting curve analysis due to sequence variation
Trevor P Anderson1, Anja M Werno, Kirsten A Beynon
1Microbiology Unit, Canterbury Health Laboratories, Christchurch, New Zealand. Trevor.Anderson@cdhb.govt.nz
Journal of Clinical Microbiology
|May 8, 2003
Abstract:
Real-time PCR with melting curve analysis of PCR products is a rapid procedure for detecting and genotyping herpes simplex virus (HSV). When testing mucocutaneous samples for HSV by a real-time PCR assay targeting the DNA polymerase gene, we found that some PCR products had atypical melting curves that did not conform to the expected melting temperatures for HSV type 1 or 2. Sequence analysis showed that these strains had base-pair mismatches over the probe binding sites. An alternative assay is required to type such atypical isolates.