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Review ArticleReview Article
Open Access

Clostridioides (Clostridium) difficile

A silent nosocomial pathogen

Ibrahim A. Al-Zahrani
Saudi Medical Journal September 2023, 44 (9) 825-835; DOI: https://doi.org/10.15537/smj.2023.44.9.20230216
Ibrahim A. Al-Zahrani
From the Department of Medical Laboratory Sciences, Faculty of Applied Medical Sciences, King Abdulaziz University, and from the Special Infectious Agents Unit-Biosafety Level-3, King Fahad Medical Research Centre, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia
MSc, PhD
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    Figure 1

    - Worldwide distribution of hypervirulent Clostridioides difficile PCR ribotype (RT) 027.

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    Table 1

    - Mechanism of action and resistance of different antimicrobials and resistance rates against Clostridioides difficile.

    AntimicrobialsTargetsPutative resistance mechanism (S)Resistances (%)Refrences
    MetronidazoleBacterial DNAAlterations in some metabolic pathways, biofilm formation0-20.2532,33,36,41
    VancomycinBinding to D-alanyl-D-alanine residues precursor of peptidoglycanMutations in peptidoglycan biosynthesis-required proteins, biofilm formation0-4132,33,36,41
    RifampicinBacterial DNA-dependent RNA polymeraseMutations in rpoB0-9132,36,41
    Clindamycin50s ribosomal subunit of bacteriaAlterations in ribosomal target or active efflux pumps0-10026,32,33,36,41
    Erythromycin50s subunit of the bacteriaAlterations in ribosomal target or active efflux pumps0-10026,32,33,36,41
    Tetracycline30S ribosomal subunit of bacteriaTetracycline resistance protein (tetM) and the active efflux pumps0-62.726,32,33,36,41
    MoxifloxacinBacterial DNA gyraseAlteration of the drug target0-10032,33,41
    Fusidic acidBlocking the ribosome by binding to “factor G”Mutations in fusA0-4041
    CiprofloxacinBacterial DNA gyraseAlteration of the drug target and the active efflux pumps23-4233,41
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    Table 2

    - Simplified comparison of various laboratory detection methods for the detection of Clostridioides difficile infection.

    TechniquesCriteriaAdvantagesLimitationsReferences
    Simple to performSimple to interpretSpecimen typeTurnaround timeSensitivity (%)Specificity (%)
    TCGoodGoodStool2-7 daysHighLowDue to its high sensitivity, it is recommended as a reference method; it allows performing strain typing and antimicrobial suitability testLong turnaround time; need to be combined with another method8,18,85
    CTAFairGoodStool filtrate48-72 hoursHighHighHas acceptable sensitivity and specificity, and it is inexpensiveLabor-intensive, long turnaround time, and lack of harmonization18,85,86
    EIA for detecting GDHGoodGoodStoolRapid 2-6 hoursLowLowQuick to produce results, and simple to useLacks specificity, high false-positive rate, and should be used in combination with another method8,18,85,87
    EIA for detecting toxins A or BGoodGoodStoolRapid 2-6 hoursLowModerateQuick to produce results, and simple to useInsensitive enough in the detection of toxin-producing isolates of C. difficile in comparison to other techniques such as TC or CTA. High false-negative rate8,18,85,87
    NAATGoodGoodStoolRapid 2 hoursHighLow/moderateRapid and highly sensitiveIdentify carriers of toxigenic C. difficile who have no symptoms. Genetic variation in tcdB or tcdA genes might lead to false-negative results. Expensive8,85,87,90
    • TC: toxigenic culture, CTA: cell cytotoxicity assay, GDH: glutamate dehydrogenase, NAAT: nucleic acid amplification test, EIA: enzyme immunoassay

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Saudi Medical Journal: 44 (9)
Saudi Medical Journal
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1 Sep 2023
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Clostridioides (Clostridium) difficile
Ibrahim A. Al-Zahrani
Saudi Medical Journal Sep 2023, 44 (9) 825-835; DOI: 10.15537/smj.2023.44.9.20230216

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Clostridioides (Clostridium) difficile
Ibrahim A. Al-Zahrani
Saudi Medical Journal Sep 2023, 44 (9) 825-835; DOI: 10.15537/smj.2023.44.9.20230216
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Keywords

  • C. difficile
  • nosocomial infection
  • C. difficile infection
  • PCR ribotype 027
  • infection control

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