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. 2005 Jul;43(7):3213–3220. doi: 10.1128/JCM.43.7.3213-3220.2005

TABLE 1.

Detection of virulence genes in E. coli ONT:H25 and O157:H25 strains by PCR

Genea Primers (5′ to 3′) and fragment size (reference)b Gene detected in:
E. coli ONT:H25c
E. coli O157d
SH1 SH2 SH3 W1 W2
eaeA F, GTGGCGAATACTGGCGAGACT + + + + +
R, CCCCATTCTTTTTCACCGTCG
890 bp (20)
stx1 F, ACACTGGATGATCTCAGTGG + +
R, CTGAATCCCCCTCCATTATG
614 bp (21)
stx2 F, CCATGACAACGGACAGCAGTT + + + + +
R, CCTGTCAACTGAGCA(GCA)CTTTG
779 bp (21)
tir F, CATTACCTTCACAAACCGAC + + + + +
R, CCCCGTTAATCCTCCCAT
1550 bp (29)
hylA F, ACGATGTGGTTTATTCTGGA + + + + +
R, CTTCACGTGACCATACATAT
165 bp (19)
fliCh7 F, GCGCTGTCGAGTTCTATCGAGC + +
R, CAACGGTGACTTTATCGCCATTCC
625 bp (25)
a

eaeA, stx1, stx2, tir, hlyA, and fliCh7 refer to the genes which encode intimin, Shiga toxin type 1, Shiga toxin type 2, translocated intimin receptor, EHEC-hemolysin, and H7 flagellar antigen, respectively.

b

F, forward primer; R, reverse primer. Predicted size of amplified product is indicated in bases; the corresponding reference is indicated in parentheses.

c

Three strains of E. coli ONT:H25 isolated in this study, designated as SH1, SH2, and SH3. One hundred percent of 258 individual isolates representing these strains gave identical results.

d

Two different E. coli strains isolated in this study, designated as W1 and W2.

HHS Vulnerability Disclosure