Abstract

Shiga toxin-producing Escherichia coli (STEC) are foodborne pathogens that cause illnesses in humans ranging from mild to hemorrhagic enteritis with complications of hemolytic uremic syndrome and even death. Cattle are a major reservoir of STEC, which reside in the hindgut and are shed in the feces, a major source of food and water contaminations. Seven serogroups, O26, O45, O103, O111, O121, O145 and O157, called ‘top-7’, are responsible for the majority of human STEC infections in North America. Additionally, 151 serogroups of E. coli are known to carry Shiga toxin genes (stx). Not much is known about fecal shedding and prevalence and virulence potential of STEC other than the top-7. Our primary objectives were to identify serogroups of STEC strains, other than the top-7, isolated from cattle feces and subtype stx genes to assess their virulence potential. Additional objective was to develop and validate a novel multiplex PCR assay to detect and determine prevalence of six serogroups, O2, O74, O109, O131, O168, and O171, in cattle feces. A total of 351 strains, positive for stx gene and negative for the top-7 serogroups, isolated from feedlot cattle feces were used in the study. Of the 351 strains, 291 belonged to 16 serogroups and 60 could not be serogrouped. Among the 351 strains, 63 (17.9%) carried stx1 gene and 300 (82.1%) carried stx2, including 12 strains positive for both. The majority of the stx1 and stx2 were of stx1a (47/63; 74.6%) and stx2a subtypes (234/300; 78%), respectively, which are often associated with human infections. A novel multiplex PCR assay developed and validated to detect six serogroups, O2, O74, O109, O131, O168, and O171, which accounted for 86.9% of the STEC strains identified, was utilized to determine their prevalence in fecal samples (n = 576) collected from a commercial feedlot. Four serogroups, O2, O109, O168, and O171 were identified as the dominant serogroups prevalent in cattle feces. In conclusion, cattle shed in the feces a number of STEC serogroups, other than the top-7, and the majority of the strains isolated possessed stx2, particularly of the subtype 2a, suggesting their potential risk to cause human infections.

Highlights

  • Shiga toxin-producing Escherichia coli (STEC) are foodborne pathogens that cause illnesses in humans ranging from mild to hemorrhagic enteritis with complications of hemolytic uremic syndrome and even death

  • Shiga toxin-producing Escherichia coli (STEC) are major foodborne pathogens responsible for human illnesses ranging from mild enteritis to hemorrhagic colitis, which in a few cases lead to complications, including hemolytic uremic syndrome (HUS) and even d­ eath[1,2,3]

  • We developed and validated a novel multiplex PCR (mPCR) assay of the six most common non-top-7 STEC O-groups (O2, O74, O109, O131, O168, and O171) to determine their prevalence in cattle feces collected from a commercial feedlot

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Summary

Introduction

Shiga toxin-producing Escherichia coli (STEC) are foodborne pathogens that cause illnesses in humans ranging from mild to hemorrhagic enteritis with complications of hemolytic uremic syndrome and even death. Our primary objectives were to identify serogroups of STEC strains, other than the top-7, isolated from cattle feces and subtype stx genes to assess their virulence potential. Cattle shed in the feces a number of STEC serogroups, other than the top-7, and the majority of the strains isolated possessed stx[2], of the subtype 2a, suggesting their potential risk to cause human infections. Prevalence of Shiga toxin types and subtypes of serogroups, which are shed in cattle feces but not commonly implicated in human STEC infections are not known. Our primary objectives in this study were to identify the serogroups of the 351 STEC strains isolated from cattle feces by multiplex PCR (mPCR) assays and conventional serological testing and determine subtypes of stx genes. We developed and validated a novel mPCR assay of the six most common non-top-7 STEC O-groups (O2, O74, O109, O131, O168, and O171) to determine their prevalence in cattle feces collected from a commercial feedlot

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