Dataset Information

Complete genome sequence of eight LEE-negative Shiga toxin-producing Escherichia coli strains isolated from patients with hemolytic-uremic syndrome.

ABSTRACT: Major serotypes of Shiga toxin-producing Escherichia coli (STEC) carry a locus of enterocyte effacement (LEE), which is required for attaching and effacing lesion formation. Genome information of LEE-negative STEC is scarce despite their virulence potential. We present the complete genome sequences of eight LEE-negative STEC isolates from hemolytic-uremic syndrome patients.

SUBMITTER: Kubomura A

PROVIDER: S-EPMC10793325 | biostudies-literature | 2024 Jan

REPOSITORIES: biostudies-literature

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Complete genome sequence of eight LEE-negative Shiga toxin-producing <i>Escherichia coli</i> strains isolated from patients with hemolytic-uremic syndrome.

Kubomura Akiko A Lee Kenichi K Ohnishi Makoto M Iyoda Sunao S Akeda Yukihiro Y Working Group Ehec E

Microbiology resource announcements 20231220 1

Major serotypes of Shiga toxin-producing <i>Escherichia coli</i> (STEC) carry a locus of enterocyte effacement (LEE), which is required for attaching and effacing lesion formation. Genome information of LEE-negative STEC is scarce despite their virulence potential. We present the complete genome sequences of eight LEE-negative STEC isolates from hemolytic-uremic syndrome patients. ...[more]

PMID: 38117079

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Project description:BackgroundShiga toxin-producing Escherichia coli (STEC) infections are leading causes of pediatric acute renal failure. Identifying hemolytic uremic syndrome (HUS) risk factors is needed to guide care.MethodsWe conducted a multicenter, historical cohort study to identify features associated with development of HUS (primary outcome) and need for renal replacement therapy (RRT) (secondary outcome) in STEC-infected children without HUS at initial presentation. Children aged <18 years who submitted STEC-positive specimens between January 2011 and December 2015 at a participating study institution were eligible.ResultsOf 927 STEC-infected children, 41 (4.4%) had HUS at presentation; of the remaining 886, 126 (14.2%) developed HUS. Predictors (all shown as odds ratio [OR] with 95% confidence interval [CI]) of HUS included younger age (0.77 [.69-.85] per year), leukocyte count ≥13.0 × 103/μL (2.54 [1.42-4.54]), higher hematocrit (1.83 [1.21-2.77] per 5% increase) and serum creatinine (10.82 [1.49-78.69] per 1 mg/dL increase), platelet count <250 × 103/μL (1.92 [1.02-3.60]), lower serum sodium (1.12 [1.02-1.23 per 1 mmol/L decrease), and intravenous fluid administration initiated ≥4 days following diarrhea onset (2.50 [1.14-5.46]). A longer interval from diarrhea onset to index visit was associated with reduced HUS risk (OR, 0.70 [95% CI, .54-.90]). RRT predictors (all shown as OR [95% CI]) included female sex (2.27 [1.14-4.50]), younger age (0.83 [.74-.92] per year), lower serum sodium (1.15 [1.04-1.27] per mmol/L decrease), higher leukocyte count ≥13.0 × 103/μL (2.35 [1.17-4.72]) and creatinine (7.75 [1.20-50.16] per 1 mg/dL increase) concentrations, and initial intravenous fluid administration ≥4 days following diarrhea onset (2.71 [1.18-6.21]).ConclusionsThe complex nature of STEC infection renders predicting its course a challenge. Risk factors we identified highlight the importance of avoiding dehydration and performing close clinical and laboratory monitoring.

Dataset Information

Complete genome sequence of eight LEE-negative Shiga toxin-producing Escherichia coli strains isolated from patients with hemolytic-uremic syndrome.

Publications

Complete genome sequence of eight LEE-negative Shiga toxin-producing <i>Escherichia coli</i> strains isolated from patients with hemolytic-uremic syndrome.

Similar Datasets

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