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. 2018 Dec 6;33(1):258–265. doi: 10.1111/jvim.15362

Table 1.

Quantitative reverse transcription PCR primer‐probe pairs used to detect hepatitis‐associated viruses in equine liver or serum samples

Name Specificity Sequence Source
TDAV‐UTR171F TDAV forward AGGGTTCTTCGGGTAAATCC Chandriani et al5
TDAV‐UTR336Rd TDAV reverse CCCTCGGACTGAATTrTAGGC Modified from Chandriani et al5
TDAV‐UTR274 TDAV probe ACCTCCCTCACGAAAGGTCGCCAC Current study
QANTI‐5UF1 NPHV forward GAGGGAGCTGRAATTCGTGAA Burbelo et al32
QANTI‐5UR1 NPHV reverse GCAAGCATCCTATCAGACCGT Burbelo et al32
NPHV‐UTR288 NPHV probe CCACGAAGGAAGGCGGGGGC Burbelo et al32
EPgV‐80F EPgV forward1 ACCGAGCCGCCCTGTAG Current study
EPgV‐163R EPgV reverse1 CCTGCCACCGCGATCA Current study
EPgV‐UTR122 EPgV probe1 TCCTGGCACTGGCCCGAAGC Current study
EPgV‐127F EPgV forward2 GCACTGGCCCGAAGCAT Current study
EPgV‐210R EPgV reverse2 CTGCCCTAACACAATCACAACAC Current study
EPgV‐UTR165 EPgV probe2 TTCTTCGGGTAAATCCCGGCCG Current study
EqPV‐3218F EqPV‐H forward ATGCAGATGCTTTCCGACC Current study
EqPV‐3386R EqPV‐H reverse GCCCCAGAAACATATGGAAA Current study
EqPV‐3310 EqPV‐H probe ACCGTAGCGGATTCGGGATCTGC Current study

Abbreviations: EPgV, equine pegivirus; EqPV‐H, equine parvovirus‐hepatitis; NPHV, non‐primate hepacivirus; TDAV, Theiler's disease–associated virus.