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. 2004 Jun;72(6):3218–3227. doi: 10.1128/IAI.72.6.3218-3227.2004

TABLE 1.

Bacterial strains, plasmids, and primers used in this study

Strain, plasmid, or primer Genotype, description, or sequence Reference or source
EPEC strains
    E2348/69 Wild-type 0127:H7
    UMD874 espF deletion mutant 23
    E2348/69 cesF cesF disruption mutant 9
EHEC strains
    EDL933 Wild-type O157:H7 Stx+
    85-170 O157:H7 ΔStx 37
    GH143 cesF::Kan derivative of 85-170 This study
    GH145 espF deletion derivative of 85-170 This study
Plasmids
    pUC 18 Cloning vector
    pDEST17 Cloning vector Invitrogen
    pKO3 Counterselectable vector 21
    pVK4 Source of Kan cassette 39
    pMP2 Intermediate for pMP5 construction This study
    pMP3 Intermediate for pMP4 construction This study
    pMP4 Plasmid used to generate GH143 (EHEC ΔcesF) This study
    pMP5 Plasmid used to generate GH145 (EHEC ΔespF) This study
    pIS4 EPEC espF in pDEST17 to produce His-tag protein This study
    pVK166 Full-length EHEC espF in pUC18 This study
    pSL1 Full-length EHEC espF in pUC18 This study
    pVK167 Full-length EHEC U-espF in pUC18 This study
Primers
    PF1 GGCAGAATTCATGCTTAATGGAATTAGTAA
    PF3 AATTCTGCAGTTACCCTTTCTTCGATTGCT
    PF6 AAAAGCAGGCTTTATGCTTAATGGAATTAG
    PF7 AGAAAGCTGGGTTTACCCTTTCTTCGATTGC
    PF10 GGTAGAATTCATGATTAACAATGTTTCTTC
    PF11 TATACTGCAGTCACGAGCGCTTAGATGTAT
    PF18 NNNNCTGCAGTTAAATGCCATGCTCTGCAAGATG
    PF25 GGGGCGGCCGCCTGGGTAATTGATCATGGTC
    PF26 TCGACTAGTGATACCTACAAGCTGCCGCC
    PF27 CATGAATTCGCCTATGAGCAATCGAAGAA
    PF28 CACGTCGACCTGAATAACACATCCCCGTC
    PF29 TGGCCTGCAGCATTAAAAATCGTCCTCGCA
    SF5 ACAGGGATCCGGAGTTGGTTAGTCAGTTTG
    SF6 ATGAGGATCCAGAGAGAAGGTGCTGGATTG
    16S-F ACTCAAATGAATTGACGGGGGC
    16S-R AGGCCCGGGAACGTATTCAC