Research Article

Immunogenicity and Protective Efficacy of a Polyvalent DNA Vaccine against Human Orthopoxvirus Infections Based on Smallpox Virus Genes

Table 1

Primers used to amplify VARV genes by PCR.

VARV genePrimer sequenceAmplicon size (bp)DNA vaccine

A30L5′-CCCGG CTAGC CGCCACC ATGGACGGAACTCTTTTCCCTG-3′360pBKRSV-A30L
5′-CCCGT CGACGTTACTCATATGGGCGCCGAC-3′pcDNA-A30L
A36R5′-CCCGGCTAGC CGCCACC ATGATGACACCAGAAAACGAC-3′581pBKRSV-A36R
5′-CCCGT CGAC TTAGTTCATTGTTTTAACACAAAAAT-3′pcDNA-A36R
B7R5′-CCCGGCTAGC CGCCACC ATGAAAACGATTTCCGTTGTTA-3′992pBKRSV-B7R
5′-CCCGT CGACACGGATTTATATTCACAGCAACA-3′pcDNA-B7R
F8L5′-CCCGGCTAGC CGCCACC ATGTCACAACAACTATCTCCTA-3′944pBKRSV-F8L
5′-CCCGT CGACAATCTAGTTTTGTTTTTCTCG-3′pcDNA-F8L
M1R5′-CCCCGCTAGC CGCCACC ATGGGTGCCGCGGCAAG-3′781pBKRSV-M1R
5′-CCCCGTCGACTTCAGTTTTGTATATCCGTGGTAGCAAT-3′pcDNA-M1R

AsuNHI (GCTAGC) and SalI (GTCGAC) sites for cloning sequence are boldfaced; initiation and stop codons are underlined; a Kozak sequence added between the initiation codon and protein sequence is italicized.