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Table 2 Details of the primers used for the molecular detections and quantifications of CEVd and HSVd

From: Multiplex detection, distribution, and genetic diversity of Hop stunt viroid and Citrus exocortis viroid infecting citrus in Taiwan

Primer pairs for multiplex RT-PCR

Primer name

Sequence 5′-3′

Product size (nt)

Position

Description

References

CEVd-dF28

GCTCVCCYGACCCYGCRa

371

28-44

Full-length cDNA for sequencing and qPCR

This work

CEVd-dR27

HCCACAGGRACCTCAAGa

11-27

CEVd-F194

TTTCGCTGCTGGCTCCACA

196

194-212

RT-PCR

CEVd-R18

ACCTCAAGAAAGATCCCGA

371-18

HSVd-F1

GGGGCAACTCTTCTCAGAATCC

302

81-102

RT-PCR

[8]

HSVd-R1

GGGGCTCCTTTCTCAGGTAAGTC

58-80

Primers/Probes for multiplex real-time RT-PCR

Primer name

Sequence 5′-3′

Product size (nt)

Position

Description

References

CEVd-RTR_F

GTCGCCGCGGATCACT

64

142-159

Real-time PCR

This work

CEVd-RTR_R

CCAGCAGCGAAAGGAAGGA

187-205

HSVd-RTR_F

GGAATTCTCGAGTTGCCGCA

127

5-24

HSVd-RTR_R

CCGCGGCCCTCTCT

118-131

Probe name

Sequence 5′-3′

 

Position

5′-Labeled

CEVd-RTR_P

CCAGCGGAGAAACAG

163-177

FAM

HSVd-RTR_P

CAACTCTTCTCAGAATCC

85-102

IC

  1. aR = AG, Y = CT, H = ACT, V = ACG.