4.7 Article

Molecular Characterization of the Enterohemolysin Gene (ehxA) in Clinical Shiga Toxin-Producing Escherichia coli Isolates

Journal

TOXINS
Volume 13, Issue 1, Pages -

Publisher

MDPI
DOI: 10.3390/toxins13010071

Keywords

Shiga toxin-producing Escherichia coli; enterohemolysin; ehxA; gene diversity; hemolytic uremic syndrome; clinical significance

Funding

  1. Scandinavian Society for Antimicrobial Chemotherapy Foundation [SLS884041]
  2. National Natural Science Foundation of China [81701977]
  3. Natural Science Foundation of Guangdong Province [2018B030311063]
  4. Guangdong Basic and Applied Basic Research Foundation [2019A1515111004]

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This study showed a high prevalence and genetic diversity of ehxA among clinical STEC isolates. The ehxA genotypes (subtype B and phylogenetic group II) were associated with severe clinical symptoms, such as BD and HUS, and could be used as risk predictors. Furthermore, ehxA, together with stx and eae, can be used as a risk predictor for HUS in STEC infections.
Shiga toxin (Stx)-producing Escherichia coli (STEC) is an important foodborne pathogen with the ability to cause bloody diarrhea (BD) and hemolytic uremic syndrome (HUS). Little is known about enterohemolysin-encoded by ehxA. Here we investigated the prevalence and diversity of ehxA in 239 STEC isolates from human clinical samples. In total, 199 out of 239 isolates (83.26%) were ehxA positive, and ehxA was significantly overrepresented in isolates carrying stx(2a) + stx(2c) (p < 0.001) and eae (p < 0.001). The presence of ehxA was significantly associated with BD and serotype O157:H7. Five ehxA subtypes were identified, among which, ehxA subtypes B, C, and F were overrepresented in eae-positive isolates. All O157:H7 isolates carried ehxA subtype B, which was related to BD and HUS. Three ehxA groups were observed in the phylogenetic analysis, namely, group ? (ehxA subtype A), group II (ehxA subtype B, C, and F), and group (ehxA subtype D). Most BD- and HUS-associated isolates were clustered into ehxA group II, while ehxA group ? was associated with non-bloody stool and individuals >= 10 years of age. The presence of ehxA + eae and ehxA + eae + stx(2) was significantly associated with HUS and O157:H7 isolates. In summary, this study showed a high prevalence and the considerable genetic diversity of ehxA among clinical STEC isolates. The ehxA genotypes (subtype B and phylogenetic group II) could be used as risk predictors, as they were associated with severe clinical symptoms, such as BD and HUS. Furthermore, ehxA, together with stx and eae, can be used as a risk predictor for HUS in STEC infections.

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