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. 2014 Apr;88(8):4008–4020. doi: 10.1128/JVI.03594-13

TABLE 1.

Primers used in this study

Primer Sequence (5′–3′) Usage
3Dpol-F1 TTTCATCGTCGGCACTCACTC Sequencing of the full-length 3Dpol-encoding gene
3Dpol-F2 TGCGCTGATTGACTTCGAGAAC
3Dpol-R GGAATGTGGAAGCGGGAAAAG
D5N-mu-F CGAGGGATTGGTTGTTAACACCAGAGATGTGGG Production of the D5N mutant
D5N-mu-R CTCCACATCTCTGGTGTTAACAACCAATCCCTCG
A38V-mu-F GAATTTGGGCCTGCTGTCTTGTCCAACAAGGAC Production of the A38V mutant
A38V-mu-R GTCCTTGTTGGACAAGACAGCAGGCCCAAATTC
M194I-mu-F CACATTCTTTACACCAGGATTATGATTGGCAGATTTTGGC Production of the M194I mutant
M194I-mu-R GCACAAAATCTGCCAATCATAATCCTGGTGTAAAGAATGTG
M296V-mu-F CATTGTTGTTGAGGGCGGGGTGCCGTCTGGCTGTTCCGC Production of the M296V mutant
M296V-mu-R GCGGAACAGCCAGACGGCACCCCGCCCTCAACAACAATG
Real-time-F AATGCACTCAAACAACGGAC Quantitative real-time PCR for detecting RNA synthesis
Real-time-R GCAGTGGTTAGCATCAAAGG
Di-Fitness-F1 TTTCATCGTCGGCACTCACTC Amplification of 3D for the direct fitness assay
Di-Fitness-F2 TGCGCTGATTGACTTCGAGAAC
Indi-Fitness-F CGCGCAAGAGACAGCAGATGG Amplification of 3A to 3D for the indirect fitness assay
Indi-Fitness-R GGAATGTGGAAGCGGGAAAAG
Mu-frequency-F TGTCCAACCTTCCTCCGCTTC Amplification of VP3 for the mutation frequency assay