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. 2018 Jun 13;92(13):e00251-18. doi: 10.1128/JVI.00251-18

TABLE 2.

Synthetic oligonucleotide primers used in the studya

Oligonucleotide Sequenceb
sORF2-393F CGCGGATCCGCAGTTATTTTACTCC
sORF2-407F CGCGGATCCGGAGCCGACAGTAAAA
sORF2-411F CGCGGATCCGCTCTACACTTCAGTC
sORF2-458F CGCGGATCCGTCTCGTCCTTTCTCT
sORF2-464F CGCGGATCCGTCCTTCGTGCCAAT
sORF2-527F CGCGGATCCGACCATCCAGCAGTAT
sORF2-526R CCCAAGCTTTCAAGTGAGCGGGCGACC
sORF2-660R CCCAAGCTTTCAATACTCCCGGGT
sORF2-624R CCCAAGCTTTCAATCAAAAGTATGGGC
sORF2-628R CCCAAGCTTTCAAGGGCAGAAATCATC
sp239-F CCCCCATATGATAGCGCTAACTTTGT
sp239-R TTCCAAGCTTTCACGCAGTATGGGGGGCG
Sar-55-239-F CCCCCATATGATAGCGCTTACCCTGT
Sar-55-239-R TTCCAAGCTTTCACACAGAGTGGGGGGCT
Kernow C1-239-F CCCCCATATGATCGCCCTGACACTGT
Kernow C1-239-R TTCCAAGCTTTCAGGCCGAGTGTGGGGCT
rHEV-239-F CCCCCATATGATAGCCCTGACGCTGT
rHEV-239-R TTCCGGATCCTCAGACAGAATGTGGAGCG
a

The oligonucleotide primers were used for cloning and expression of different truncated fragments of genotype 4 swine HEV capsid protein and target regions of amino acids 368 to 606 of capsid proteins from various swine, human, and rabbit HEV strains.

b

Underlining indicates BamHI, NdeI, or HindIII sequences.