Table 4.: Genomic Sequence Alignment of Selected CV Strains around the Reverse Primer

Straina Sequenceb
X05690 CATTTCTGACAATGCATCTGGGAACTTCCACCACCACCCC
AF311939 CATCTCTGACAGCGCATCTGGGAACTTCCACCACCACCCC
AF114384 CATATTGGACAGCGCATCAGGAAACTTCCACCACCACCCT
AF081485 CATGTCTGATAGTGCGTCGGGAAACTTCCACCACCAACCA
AF085363 CATGTCTGATAGTGCGTCGGGAAACTTCCACCACCAACCA
AY186748 CATTTGCGATAGCGCATCTGGCAGTTTCCACCACCACCCA
AY186746 CATTTGCGATAGCGCATCTGGCAGTTTCCACCACCACCCA
M16560 CATTTGTGAAAGTGCATCTGGTAACTTCCACCACCAACCT
M88483 TAAGTTCGACAAAGCATCGGGCAGCTTCCACCACCATCCT
AF231764 TAAGTTCGACAAAGCATCGGGCAGCTTCCACCACCATCCT
U57056 TAAGTTCGACAAAGCATCAGGCAGCTTCCACCACCATCCT
D00627 CATATCACTAAGCGCTTCTGGGAACTTCCACCACCACCCC
AF177911 TACTTCTGTCAAAACATCAGGGAATTTCCAATACCATCCC
reverse primer TCDGGNARYTTCCACCACCA

a CV strains are identified by their GenBank accession number.
b CV sequence alignment is presented as the reverse complement (antisense) of the genomic strand in 5’ to 3’ orientation. The primer sequence and nucleotide identity is based on the genomic sequence and nucleotide numbering of CVB1 (M16560) at nucleotide positions 1199 to 1180. The primer is degenerate where D equals A, G, or T; N equals A, G, C, or T; R equals A or G; and Y equals C or T, respectively.