AI Article Synopsis

  • Clostridium difficile is a leading cause of antibiotic-associated diarrhea and is a significant financial burden in healthcare settings.
  • This study analyzed fecal samples from children under 5 years old, revealing that 52% of diarrheic samples tested positive for C. difficile, with a much lower prevalence in healthy children.
  • The highest prevalence was found in children aged 13 to 24 months, and specific ribotypes were identified, indicating a need for ongoing monitoring of C. difficile strains to inform future vaccine development.

Article Abstract

Clostridium difficile is recognized as a major cause of nosocomial acquired antibiotic-associated diarrhea and pseudomembranous colitis. It is a significant financial burden on modern healthcare resources. This study aimed to assess the molecular characterization of C. difficile strains isolated from children under 5 years old suffered from nosocomial diarrhea. One hundred diarrheic and 130 non-diarrheic fecal samples were collected from pediatrics less than 5 years old. Samples were cultured and C. difficile isolates were subjected to the PCR technique to study the distribution of ribotypes of C. difficile using P3 and P5 primers. Fifty-two out of 100 samples (52 %) were positive for C. difficile. The prevalence of bacterium in healthy children was 4.61 %. Total prevalence of C. difficile in diarrheic girls and boys were 48.9 and 54.7 %, respectively. Thirteen to twenty-four month age children had the highest prevalence of C. difficile. The most commonly detected ribotypes in the C. difficile isolates of Iranian pediatrics were RT027 (11.52 %), R1 (9.61 %) and R13 (7.68 %). The ribotypes of all of the six bacterial isolates of healthy children was not diagnosed. According to the presence of C. difficile and R27 ribotype, a continued genotype surveillance of this bacterium is necessary to monitor changes in the prevalence of certain strains and to identify the emergence of new strains that could affect future vaccine strategies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4628048PMC
http://dx.doi.org/10.1186/s40064-015-1268-0DOI Listing

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