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A Protein Microarray Assay for Serological Determination of Antigen-specific Antibody Responses Following Clostridium difficile Infection
Published on: June 15, 2018
Optimized Surveillance Testing for Toxigenic Clostridioides difficile to Scale Prevention Programs Across Clinical
Medrxiv : the Preprint Server for Health Sciences
|August 1, 2026
Summary
A new method uses rectal swabs for Clostridioides difficile (C. difficile) surveillance, improving detection of toxigenic strains. This scalable approach aids healthcare systems in preventing C. difficile infections.
Area of Science:
- Clinical Microbiology
- Infectious Diseases
- Healthcare Epidemiology
Background:
- Clostridioides difficile (C. difficile) infections are a leading cause of healthcare-associated infections (HAIs).
- Current surveillance strategies for toxigenic C. difficile are not scalable for clinical microbiology laboratories.
- Effective prevention programs require scalable methods to identify patients colonized with toxigenic C. difficile strains.
Purpose of the Study:
- To develop and validate a scalable surveillance strategy for detecting toxigenic C. difficile colonization.
- To utilize existing rectal swabs collected for vancomycin-resistant Enterococci (VRE) surveillance.
- To enhance C. difficile prevention programs through improved patient identification.
Main Methods:
- Developed a two-step method involving ex vivo amplification in Cdiff Banana Broth (BB) followed by confirmatory testing.
- Optimized confirmatory testing using C. difficile QuickCheck and Cepheid's Xpert C. difficile/Epi assay.
- Evaluated the method's sensitivity, specificity, and performance on VRE surveillance swabs from diverse healthcare settings.
Main Results:
- The BB with confirmation method demonstrated 92% specificity and 100% sensitivity, detecting toxigenic C. difficile at <5 CFU/swab.
- Prospective testing of 797 VRE swabs revealed 11% positivity for toxigenic C. difficile and 4% for non-toxigenic strains.
- The method allowed for C. difficile detection within 24-48 hours and preserved viability for 7 months with glycerol addition.
Conclusions:
- BB with confirmation offers a highly sensitive and scalable approach for detecting toxigenic C. difficile colonization.
- Leveraging VRE surveillance swabs eliminates the need for additional patient samples, simplifying deployment.
- This strategy can be implemented across healthcare settings to support C. difficile infection prevention initiatives.
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