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Genotypic analysis of pseudoepidemic due to contamination of Hanks' balanced salt solution with Candida parapsilosis

S C Deresinski1, K V Clemons, C A Kemper

  • 1Department of Medicine, Santa Clara Valley Medical Center, San Jose, California 95128, USA.

Insights

A laboratory contamination, not a true Candida parapsilosis outbreak, was identified using molecular techniques. The source was a contaminated Hanks

Area of Science:

  • Clinical Microbiology
  • Infectious Diseases
  • Epidemiology

Background:

  • Candida parapsilosis is an opportunistic fungal pathogen causing infections, particularly in healthcare settings.
  • Distinguishing true outbreaks from laboratory contamination is crucial for accurate patient management and infection control.

Purpose of the Study:

  • To investigate a cluster of Candida parapsilosis isolates from clinical specimens.
  • To determine the source and nature of the observed isolate cluster, differentiating between a true pseudoepidemic and laboratory error.

Main Methods:

  • Classical microbiological techniques were employed for isolate characterization.
  • Molecular epidemiological methods, including DNA extraction and restriction fragment length polymorphism (RFLP) analysis, were utilized.
  • Environmental sampling and analysis were performed to identify the contamination source.

Main Results:

  • A cluster of Candida parapsilosis isolates from clinical specimens was confirmed to be due to laboratory contamination.
  • The contamination originated from a reusable container of Hanks' balanced salt solution used in specimen processing.
  • DNA fingerprinting (RFLP) revealed identical patterns among clinical and environmental isolates, representing a unique Candida parapsilosis DNA type.

Conclusions:

  • Laboratory procedures can lead to pseudoepidemics, mimicking true outbreaks of Candida parapsilosis.
  • Rigorous quality control and aseptic techniques in laboratories are essential to prevent specimen contamination.
  • The identification of a unique DNA type highlights the importance of molecular tools in tracing microbial sources.

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