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. 2005 May;73(5):2818–2827. doi: 10.1128/IAI.73.5.2818-2827.2005

TABLE 1.

Oligonucleotide primers used in this study and results of PCRs to detect genes of pathogenicity island

Primer Sequence (5′-3′) Presence of genea
P2 TACCTACAACCTCAAGCT
P4 TACCCATTCTAACCAAGC
P6 CCTAGGCGGCCAGATCTGAT
P7 GCACTTGTGTATAAGAGTCAG
P9 CGCAGGGCTTTATTGATTC
Arbi1 GGCCACGCGTCGACTAGTAC(N)10 GATAT
Arbi2 GGCCACGCGTCGACTAGTAC
Arbi3 GGCCACGCGTCGACTAGTAC(N)10 TGACG
Arbi4 GGCCACGCGTCGACTAGTAC(N)10 ACGCC
Arbi5 GGCCACGCGTCGACTAGTAC(N)10 TACNG
P19 ATTCAACGGGAAACGTCTTG
P20 ACTGAATCCGGTGAGAATGG
PapG-F TTTGCGAGTGGAGTGTATTT
PapG-R TACCTAACCCAACCGAAAAT
PapC-F TGATATCACGCAGTCAGTAGC
PapC-R CCGGCCATATTCACATAA
R14-15-F GCCAGTGACACATACTGAGAGC +
R14-15-R CAGATGTACAGTGGCGCG
R2 plus R3-F GCTGTCAGAATATTTCGCTCG +
R2 plus R3-R AGTCCTGTCACGCTGAACG
R1 plus R2-F AGCCTTTCTGTTTTGAGCAT +
R1 plus R2-R TCGCTACTATTGATTCTTGC
R1 plus f447-F CCGCAAGAATCAATAGTAGC +
R1 plus f447-R CTGGCGAGAAGGGGATAATG
a

PCR elaborated for detection of metV genomic island.