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. 2004 Jun 17;325(2):308–319. doi: 10.1016/j.virol.2004.04.046

Table 1.

Primers used in the present study

Primer Sequencea Viral genome positionb
For fragment A
 P1F 5′GCATATAAGCTTTAATACGACTCACTATAGGTGCCTCGGCAT TTGTATTGTCAGG 24–47
 P1146R 5′GTGTCAGTCGACGTAGATGTACAACGATAGGCCCATC 1155–1174
 T7P+1 5′ATATAAGCTTCGGACCGTAATACGACTCACTATAGGATGACGTATAGGTGTTGGCTCTATGCCATGACATTTGTATTG 1–42
For fragment B
 P1145F 5′GTGTCAGATATCTGTACAGTACTTCTCTG 1169–1185
 P6154R 5′GTGTCAGATATCAGCCCATATGTCTTTAATTATGTGGC 6157–6178
For fragment 5C
 P5706F 5′ATATAGATATCGCACATGTCCTTACGGG 5730–5746
 P9791R 5′ATATAGATATCCATCTAGAGGGCTTGTGC 9798–9815
For fragment 3C
 P9783F 5′ATATAGGATCCCTCTAGATGAGGTGTTG 9805–9823
 P13625R 5′ATATAGGATCCCTTGACATGTTGGACGTAGC 13640–13660
For fragment D
 P12687F 5′GTGTCAAAGCTTGTACATTCCTCCATATTTTCCTCC 12710–12734
 P15393RpolyA 5′GTGTCAGTCGACGCGTTTTTTTTTTTTTTTTTTTTTTTTTTTT TTTTTTTTTTTTTAATTTCGGCCGCATGGTTCTCGC 15391–15454
For genetic Tag
 P24F 5′TGCCTCGGCATTTGTATTGTC 24–44
 P1763R 5′CACATTCAAGGGGGAGCAGAGAAG 1741–1764
a

T7 RNA polymerase promoter sequence is italicized. Underlined sequences represent restriction enzyme recognition sites utilized in full-length cDNA assembly. PRRSV-specific sequences are in bold-face type.

b

Nucleotide position within the NVSL#97-7895 PRRSV isolates consensus full-length genome.