Is reporting Escherichia coli (E. coli) O157:H7 without Shiga toxin (stx) clinically useful?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: August 13, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Clinical Utility of Reporting E. coli O157:H7 without Shiga Toxin

Reporting E. coli O157:H7 isolates is clinically important regardless of Shiga toxin status, as stx-negative strains can still cause diarrheal illness and retain other virulence factors. 1

Rationale for Reporting O157:H7 Without Shiga Toxin

Clinical Significance

  • Stx-negative E. coli O157:H7 strains can cause diarrheal illness, though typically with less severity than Shiga toxin-producing strains 1
  • These strains retain other virulence factors, including the locus of enterocyte effacement (LEE) region that contributes to pathogenicity 1
  • Studies have documented stx-negative E. coli O157:H7 isolates from patients with diarrhea (4% of sporadic cases) and even hemolytic uremic syndrome (HUS) 2

Diagnostic Algorithm

  1. Initial identification: When E. coli O157:H7 is identified through agglutination with O157-specific reagents and biochemical confirmation
  2. Preliminary reporting: Report immediately to clinicians before complete confirmation, as this is time-sensitive clinical information 3
  3. Shiga toxin testing: Test for Shiga toxin production by EIA or for stx1/stx2 genes by PCR 3
  4. Final reporting: Provide complete report including Shiga toxin status to clinician and public health authorities 3

Public Health Implications

  • All O157 isolates should be forwarded to public health laboratories regardless of H7 or Shiga toxin status 3
  • Prompt reporting enables:
    • Outbreak detection and monitoring
    • Implementation of appropriate infection control measures
    • Molecular characterization through PFGE subtyping 3, 1

Clinical Management Considerations

Patient Care

  • The absence of Shiga toxin affects risk assessment:
    • Lower risk of developing HUS compared to Stx-positive strains 2
    • Still requires monitoring for complications and appropriate supportive care 1

Treatment Approach

  • Supportive care remains the cornerstone of management 1
  • Rehydration therapy based on dehydration severity 1
  • Even with stx-negative strains, antibiotics should be used cautiously as:
    • The strain may have lost the stx gene during infection 2
    • The patient may be co-infected with other stx-positive strains

Important Caveats

  • Stx-negative E. coli O157:H7 may represent:

    1. Inherently stx-negative strains causing mostly uncomplicated diarrhea, or
    2. Strains that descended from STEC by losing the stx gene during infection, which may still cause severe disease 2
  • Diagnostic methods targeting only Shiga toxin will miss stx-negative E. coli O157:H7 variants, potentially leading to underdiagnosis 4

  • The CDC and Infectious Diseases Society of America recommend comprehensive testing approaches for all stools from patients with acute community-acquired diarrhea to identify both toxin-positive and toxin-negative strains 1

Conclusion

Reporting E. coli O157:H7 without Shiga toxin has significant clinical utility for individual patient management, infection control, and public health surveillance. The identification of the O157:H7 serotype, regardless of toxin status, provides valuable information for clinical decision-making and public health response.

References

Guideline

E. coli O157:H7 Infections

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Prevalence, virulence profiles, and clinical significance of Shiga toxin-negative variants of enterohemorrhagic Escherichia coli O157 infection in humans.

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2007

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.