Genetic diversity of the intimin gene (eae) in non-O157 Shiga toxin-producing Escherichia coli strains in China
Shiga toxin-producing Escherichia coli (STEC) is an important foodborne pathogen. The increasing incidence of non-O157 STEC has posed a great risk to public health. Besides the Shiga toxin (Stx), the adherence factor, intimin, coded by eae gene plays a critical role in STEC pathogenesis. In this stu...
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Published in | Scientific reports Vol. 10; no. 1; pp. 3275 - 9 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
24.02.2020
Nature Publishing Group Nature Portfolio |
Subjects | |
Online Access | Get full text |
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Summary: | Shiga toxin-producing
Escherichia coli
(STEC) is an important foodborne pathogen. The increasing incidence of non-O157 STEC has posed a great risk to public health. Besides the Shiga toxin (Stx), the adherence factor, intimin, coded by
eae
gene plays a critical role in STEC pathogenesis. In this study, we investigated the prevalence and polymorphisms of
eae
gene in non-O157 STEC strains isolated from different sources in China. Among 735 non-O157 STEC strains,
eae
was present in 70 (9.5%) strains. Eighteen different
eae
genotypes were identified in 62
eae
-positive STEC strains with the nucleotide identities ranging from 86.01% to 99.97%. Among which, seven genotypes were newly identified in this study. The eighteen
eae
genotypes can be categorized into five
eae
subtypes, namely β1, γ1, ε1, ζ3 and θ. Associations between
eae
subtypes/genotypes and serotypes as well as origins of strains were observed in this study. Strains belonging to serotypes O26:H11, O103:H2, O111:H8 are associated with particular
eae
subtypes, i.e., β1, ε1, θ, respectively. Most strains from diarrheal patients (7/9, 77.8%) carried
eae
-β1 subtype, while most isolates from cattle (23/26, 88.5%) carried
eae
-ζ3 subtype. This study demonstrated a genetic diversity of
eae
gene in non-O157 STEC strains from different sources in China. |
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ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-020-60225-w |