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Related Experiment Video

Updated: Jun 19, 2026

A Protein Microarray Assay for Serological Determination of Antigen-specific Antibody Responses Following Clostridium difficile Infection
09:12

A Protein Microarray Assay for Serological Determination of Antigen-specific Antibody Responses Following Clostridium difficile Infection

Published on: June 15, 2018

Clostridium difficile testing algorithms: what is practical and feasible?

Monica L Schmidt1, Peter H Gilligan

  • 1Clinical Microbiology-Immunology Laboratories, University of North Carolina Hospitals, Chapel Hill, NC 27514, USA.

Anaerobe
|October 27, 2009
PubMed
Summary
This summary is machine-generated.

Diagnosing Clostridium difficile infections is improving with new algorithms. Combining glutamate dehydrogenase (GDH) screening with toxin tests offers a faster, more accurate diagnosis for most patients.

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A Protocol to Characterize the Morphological Changes of Clostridium difficile in Response to Antibiotic Treatment
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Last Updated: Jun 19, 2026

A Protein Microarray Assay for Serological Determination of Antigen-specific Antibody Responses Following Clostridium difficile Infection
09:12

A Protein Microarray Assay for Serological Determination of Antigen-specific Antibody Responses Following Clostridium difficile Infection

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A Protocol to Characterize the Morphological Changes of Clostridium difficile in Response to Antibiotic Treatment
12:58

A Protocol to Characterize the Morphological Changes of Clostridium difficile in Response to Antibiotic Treatment

Published on: May 25, 2017

Area of Science:

  • Clinical microbiology
  • Infectious disease diagnostics

Background:

  • Clostridium difficile infections (CDI) are increasing in incidence and severity.
  • Enzyme immunoassays (EIAs) for C. difficile toxins A and B have been standard diagnostic tools.
  • Glutamate dehydrogenase (GDH) antigen testing shows higher sensitivity than EIAs for CDI screening.

Purpose of the Study:

  • To evaluate a new diagnostic algorithm for Clostridium difficile infections.
  • To improve the accuracy and speed of CDI laboratory diagnosis.

Main Methods:

  • Utilized a testing algorithm incorporating rapid immunochromatographic devices for GDH and toxin A/B detection.
  • Employed cytotoxin neutralization as the reference method for accuracy assessment.
  • Considered confirmatory tests including cytotoxin neutralization, toxigenic culture, and PCR for toxin genes.

Main Results:

  • The proposed algorithm accurately identified CDI in approximately 90% of specimens within one hour.
  • GDH screening demonstrated superior sensitivity compared to toxin EIAs.
  • A confirmatory test was necessary for the remaining 10% of specimens to ensure diagnostic accuracy.

Conclusions:

  • A diagnostic algorithm combining GDH and toxin screening offers a rapid and accurate approach to CDI diagnosis.
  • This strategy enhances laboratory efficiency and patient management for Clostridium difficile infections.
  • Further confirmatory testing is essential for a small subset of cases to achieve definitive diagnosis.