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. 2016 Jun 13;82(13):3913–3927. doi: 10.1128/AEM.00271-16

TABLE 1.

PCR primers used in this study for stx and eae subtyping by sequencing

Gene Primer designation Primer sequence (5′–3′) Fragment size (bp) Reference or source
stx2 F4 GGCACTGTCTGAAACTGCTCCTGT 627 7
R1 ATTAAACTGCACTTCAGCAAATCC
F4-f CGCTGTCTGAGGCATCTCCGCT 625
R1-e/f TAAACTTCACCTGGGCAAAGCC
eaea EAE-F ATTACTGAGATTAAGGCTGAT 682 51
EAE-RB ATTTATTTGCAGCCCCCCAT
eae EAE-F ATTACTGAGATTAAGGCTGAT 722 51
LP5 AGCTCACTCGTAGATGACGGCAAGCG
eae EAE-F ATTACTGAGATTAAGGCTGAT 712 51
LP8 TAGATGACGGTAAGCGAC
eae EAE-F ATTACTGAGATTAAGGCTGAT 468 51
B49R ACCACCTTTAGCAGTCAATTTG
eae FV373F CAACGGTAAGTCTCAGACAC 443 51
FV373R CATAATAAGCTTTTTGGCCTACC
eae IH1229aF CACAGCTTACAATTGATAACA 311 51
IH1229aR CTCACTATAAGTCATACGACT
eaeb eae-F1 ACTCCGATTCCTCTGGTGAC ∼1,800–2,100, depending on the allele 75
escD-R1 GTATCAACATCTCCCGCCCA
eaeb cesT-F3 CAGGAGCACAATCGCTGTTG 1,727 This study
eae-R3 CAGACGATACGATCCAGACC
a

Universal primers targeting the 3′ variable regions of the eae-α1, -α2, -β1, -β2, -γ2, -θ, -δ, -κ, -ζ, and -ι subtypes.

b

Primers targeting overlapping DNA fragments of the eae gene.