Detection and toxin typing of Clostridium perfringens in formalin-fixed, paraffin-embedded tissue samples by PCR

Josephine Wu1, Wandi Zhang, Boxun Xie

  • 1Department of Pathology, Mount Sinai School of Medicine, One Gustave L. Levy Place, Box 1122, New York, New York 10029, USA.

Insights

A new PCR assay can detect Clostridium perfringens in preserved tissue samples. This method successfully identified and genotyped the bacteria in autopsy cases, overcoming limitations of traditional microbiology.

Area of Science:

  • Microbiology
  • Molecular Biology
  • Pathology

Background:

  • Traditional microbiology techniques are insufficient for detecting Clostridium perfringens in formalin-fixed, paraffin-embedded (FFPE) tissues.
  • Accurate identification of Clostridium perfringens in FFPE samples is crucial for retrospective studies and understanding disease pathogenesis.

Purpose of the Study:

  • To develop a novel Polymerase Chain Reaction (PCR) assay for the detection and genotyping of Clostridium perfringens.
  • To validate the assay's efficacy in identifying Clostridium perfringens within challenging FFPE tissue samples.

Main Methods:

  • Development of a species-specific PCR assay targeting toxin-encoding genes and the 16S rRNA gene of Clostridium perfringens.
  • Application of the PCR assay to DNA extracted from formalin-fixed, paraffin-embedded tissue sections.

Main Results:

  • The developed PCR assay successfully detected the presence of Clostridium perfringens in FFPE tissue samples.
  • The assay enabled the genotyping of Clostridium perfringens, providing further discriminatory information.
  • Successful detection and genotyping were confirmed in tissue sections from two distinct autopsy cases.

Conclusions:

  • The novel PCR assay provides a reliable method for detecting Clostridium perfringens in FFPE tissues, overcoming previous limitations.
  • This molecular approach facilitates accurate identification and characterization of Clostridium perfringens in archival pathological specimens.

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