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Related Concept Videos

Bacterial Gastroenteritis01:18

Bacterial Gastroenteritis

5
Bacterial gastroenteritis, characterized by diarrhea, abdominal cramps, and vomiting, is often caused by ingestion of contaminated food or water and is frequently associated with pathogenic Escherichia coli strains. These microbes exploit two principal mechanisms to inflict disease.Shiga toxin–producing E. coli, also referred to as STEC—notably O157:H7—release Shiga toxins that target ribosomes, blocking protein synthesis. The B subunit of the toxin binds the host glycolipid...
5

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Related Experiment Video

Updated: Mar 18, 2026

Cefoperazone-treated Mouse Model of Clinically-relevant Clostridium difficile Strain R20291
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[Relationship between Clostridium difficile ITS-PCR Type and Pathogenicity].

Yukiko Takemori, Yasuko Senda, Tomoko Munesue

    Rinsho Byori. the Japanese Journal of Clinical Pathology
    |July 2, 2016
    PubMed
    Summary

    Internal transcribed spacer region PCR typing of Clostridium difficile (C. difficile) effectively identifies nosocomial infections and assesses toxigenicity. This method aids in early detection and understanding C. difficile pathogenicity, offering a rapid classification of bacterial strains.

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    Area of Science:

    • Microbiology
    • Infectious Diseases
    • Molecular Diagnostics

    Background:

    • Clostridium difficile (C. difficile) is a significant cause of antibiotic-associated diarrhea and hospital-acquired infections.
    • Rapid and accurate typing methods are crucial for managing C. difficile outbreaks and understanding its epidemiology.

    Purpose of the Study:

    • To classify C. difficile strains using the PCR electrophoresis pattern of internal transcribed spacer regions (ITS-PCR type).
    • To investigate the relationship between ITS-PCR types and C. difficile pathogenicity, including toxin gene presence and clinical severity.

    Main Methods:

    • Seventy-seven C. difficile strains were analyzed.
    • Toxin genes (Toxin A, Toxin B, binary toxin) were detected using PCR.
    • Antimicrobial susceptibility testing was performed using E-test.
    • Clinical data, including pseudomembrane formation and illness severity, were reviewed.

    Main Results:

    • Thirty-three distinct ITS-PCR types were identified among the 77 strains.
    • Most strains (18 types) lacked detectable toxin genes.
    • Toxigenic strains (Toxin A/B positive, Toxin B positive, Toxin A/B/binary toxin positive) were associated with specific ITS-PCR types (14 types, type 17, type 16).
    • Evidence of nosocomial transmission was suggested for strains from the same ward (type 33 and type 2).
    • Antimicrobial MICs for vancomycin and metronidazole did not correlate with ITS-PCR type.
    • No clear association was found between ITS-PCR patterns and pseudomembrane formation or clinical severity.

    Conclusions:

    • ITS-PCR typing is a valuable tool for the early detection of C. difficile nosocomial infections.
    • This method aids in assessing the toxigenic potential of C. difficile strains.
    • ITS-PCR provides a rapid classification useful for epidemiological surveillance.