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Shiga toxin-producing Escherichia coli in Montana: bacterial genotypes and clinical profiles
Jill K Jelacic1, Todd Damrow, Gilbert S Chen
1University of Washington School of Medicine, Seattle, Washington, USA.
Abstract:
The diseases and virulence genes associated with Shiga toxin-producing Escherichia coli (STEC) are characterized incompletely. We analyzed, by polymerase chain reaction, 82 STEC isolates collected prospectively in Montana and profiled associated illnesses by patient chart review. All E. coli O157:H7 contained stx2-group genes, as well as eae, iha, espA, and ehxA; 84% contained stx1. Non-O157:H7 STEC less frequently contained stx1 (P=.046), stx2 (P<.001), iha (P<.001), eae, and espA (P=.039 for both), were isolated less often from patients treated in emergency departments (P=.022), and tended to be associated less frequently with bloody diarrhea (P=.061). There were no significant associations between stx genotype and bloody diarrhea, but isolates containing stx2c or stx(2d-activatable) were recovered more often from patients who underwent diagnostic or therapeutic procedures (P=.033). Non-O157:H7 STEC are more heterogeneous and cause bloody diarrhea less frequently than do E. coli O157:H7. Bloody diarrhea cannot be attributed simply to the stx genotype of the infecting organism.
Insights
Shiga toxin-producing Escherichia coli (STEC) strains vary in virulence genes. Non-O157:H7 STEC are more diverse and less frequently cause bloody diarrhea compared to E. coli O157:H7.
Area of Science:
- Microbiology
- Infectious Diseases
- Genetics
Background:
- Shiga toxin-producing Escherichia coli (STEC) infections pose significant public health risks.
- Incomplete characterization of STEC virulence factors and associated diseases hinders effective management.
- Understanding genetic diversity is crucial for predicting STEC pathogenicity.
Purpose of the Study:
- To analyze the genetic profiles of STEC isolates.
- To correlate specific virulence genes with clinical manifestations of STEC infections.
- To differentiate between E. coli O157:H7 and non-O157:H7 STEC pathogenicity.
Main Methods:
- Prospective collection of 82 STEC isolates from Montana.
- Polymerase chain reaction (PCR) for detecting virulence genes (stx1, stx2, eae, iha, espA, ehxA).
- Patient chart review to profile associated illnesses and clinical outcomes.
Main Results:
- All E. coli O157:H7 isolates possessed stx2-group, eae, iha, espA, and ehxA genes; 84% also had stx1.
- Non-O157:H7 STEC isolates showed less frequent carriage of stx1, stx2, iha, eae, and espA.
- Non-O157:H7 STEC were less often isolated from emergency department patients and tended to cause less bloody diarrhea.
Conclusions:
- Non-O157:H7 STEC are genetically more heterogeneous than E. coli O157:H7.
- The presence of specific Shiga toxin genotypes does not solely determine the occurrence of bloody diarrhea.
- Clinical outcomes of STEC infections are influenced by a complex interplay of bacterial genetics and host factors.
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