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. 2016 Aug 1;32(4):321–328. doi: 10.5423/PPJ.OA.12.2015.0259

Table 1.

Primers used to detect PVY-O, PVA, and PLRV

Primer pairs Sequence PCR type
PLRV-qPCR F 5′-CAACAACCAAGAAGGCGAAG-3′ qPCR
PLRV-qPCR R 5′-ACCATAACCACTGGCTGAACTC-3′
PLRV-186F 5′-GAGTCTATCAGACTGTCCGGCATT-3′ RT-PCR
PLRV-4391R 5′-ATTGAGAGTTAATACTCAGAG-3′
PVA-807F 5′-CCGAAACTCTTGATGCAAGCGAA-3′
PVA-807R 5′-CACCCCCTTCACGCCTAAAAGGTG-3′
PVY CP-801F 5′-GCAAATGACACAATTGATGCA-3′
PVY CP-801R 5′-CATGTTCTTGACTCCAAGTAGAGTA-3′

PVY-O, Potato virus Y-O; PVA, Potato virus A; PLRV, Potato leafroll virus.

Both PVY-O and PVA were amplified using the reverse transcription-polymerase chain reaction (RT-PCR), and absolute quantification of PLRV copies was conducted by real-time RT-PCR (qRT-PCR).