Shiga toxin-producing E. coli (STEC) is a gastrointestinal pathogen and has been recognized as one of the serious problems in public health. Shiga toxin genes (stx) can be grouped into different types according to their differences in sequence and biological activities. The two main groups of stx are stx1 and stx2 with each group containing several subtypes. It is essential to develop rapid stx1/stx2 subtyping assays and accurate stx2 general detection assays to provide a quicker turn-around time to predict disease outcome and also to provide data for surveillance purposes. The stx2 general detection qPCR assay developed in this study showed 100% sensitivity and 100% specificity with no cross reactivity with stx2 negative STEC and non-STEC isolates. This stx2 general detection assay was able to detect all seven different stx2 subtypes at low level of detection and with good PCR efficiency. In addition, stx1/stx2 subtyping qPCR assays were succesfully developed to detect all stx1 subtypes and stx2 subtypes with the exception of one stx2b subtype carried by one strain. The qPCR stx1/stx2 subtyping assays showed 100% specificity with no cross reactivity on subtypes not targeted by each assay. The rapidity with faster turn-around time along with high throughput volume of the stx1/stx2 subtyping and stx2 general detection qPCR assays will have great value as tools for STEC associated risk assessment, outbreak monitoring, epidemiology studies, and clinical management.
Keywords: General detection; Shiga toxin-producing E. coli (STEC); Subtyping; qPCR.
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