Table 1 Sequence for primers and probes in human herpes viruses (HHV) using real-time PCR
Herpes virusSequence for primers and probesAmplification
HSV1 and 2HSV-F: CGCATCAAGACCACCTCCTCgB
HSV-R: GCTCGCACCACGCGA
HSV1-P: JOE-TGGCAACGCGGCCCAAC-TAMRA
HSV2-P: FAM-CGGCGATGCGCCCCAG-TAMRA
VZVVZV-F: AACTTTTACATCCAGCCTGGCGORF29
VZV-R: GAAAACCCAAACCGTTCTCGAG
VZV-P: FAM-TGTCTTTCACGGAGGCAAACACGT-TAMRA
EBVEBV-F: CGGAAGCCCTCTGGACTTCBALF5
EBV-R: CCCTGTTTATCCGATGGAATG
EBV-P: FAM-TGTACACGCACGAGAAATGCGCC-TAMRA
CMVCMV-F: CATGAAGGTCTTTGCCCAGTACIE-1
CMV-R: GGCCAAAGTGTAGGCTACAATAG
CMV-P: FAM-TGGCCCGTAGGTCATCCACACTAGG-TAMRA
HHV6HHV6-F: GACAATCACATGCCTGGATAATGU65-U66
HHV6-R: TGTAAGCGTGTGGTAATGTACTAA
HHV6-P: FAM-AGCAGCTGGCGAAAAGTGCTGTGC-TAMRA
HHV7HHV7-F: CGGAAGTCACTGGAGTAATGACAAU37
HHV7-R: CCAATCCTTCCGAAACCGAT
HHV7-P: FAM-CTCGCAGATTGCTTGTTGGCCATG-TAMRA
HHV8HHV8-F: CCTCTGGTCCCCATTCATTGORF65
HHV8-R: CGTTTCCGTCGTGGATGAG
HHV8-P: FAM-CCGGCGTCAGACATTCTCACAACC-TAMRA
  • The real-time herpes simplex virus (HSV) PCR is a multiplexing PCR that can detect both HSV1 and HSV2 DNA in the same reaction. The optimised gB primer pairs amplify both HSV1 and 2 with equal efficiency, with the two type-specific probes labelled with different fluorescent dyes. HSV1 probe is labelled with JOE at the 5′-end and with TAMRA at the 3′-end. HSV2 probe is labelled with FAM at the 5′-end and with TAMRA at the 3′-end.

  • CMV, cytomegalovirus; EBV, Epstein–Barr virus; VZV, Varicella-zoster virus.