Skip to main content
. 2008 Feb 13;46(4):1292–1297. doi: 10.1128/JCM.02271-07

TABLE 2.

Detection of Stx in STEC strain supernatants and enriched stool cultures by conventional assays and by immuno-PCR

Sample (no. of samples) stx genotype Conventional assaysa Immuno-PCR detection of Stxb
Undiluted 1:10 1:100
STEC low producers (6) stx2dc + +
stx2ed + +
STEC controls (4) stx2de + + + +
stx2ef + + + +
stx1, stx2g + + + +
Nonproducers (20) h
Stool samples (3) stx2 + ND ND
Stool samples (10) ND ND
a

Conventional assays include the Vero cell cytotoxicity assay, the Stx enzyme immunoassay (R-Biopharm), the latex agglutination assay (VTEC-RPLA; Denka Seiken, Coventry, United Kingdom), and Stx colony immunoblotting (Sifin). +, positive result; −, negative result. Identical results were obtained with all of the conventional assays for each strain.

b

Immuno-PCR detection response to various supernatant dilutions. +, PCR product present; −, PCR product absent; ND, not done.

c

Serotypes O40:H8 (three samples), O86:H, and Orough:HNT.

d

Serotype ONT (not typeable):H.

e

Serotypes O91:H and ONT:H12.

f

Serotype ONT:H.

g

Strain EDL933 serotype O157:H7.

h

—, no stx gene was detected.