Combined stool-based multiplex PCR and microscopy for enhanced pathogen detection in patients with persistent

S L Becker1, J K Chatigre2, J-P Gohou2

  • 1Department of Epidemiology and Public Health, Swiss Tropical and Public Health Institute, Basel, Switzerland; University of Basel, Basel, Switzerland; Institute of Medical Microbiology and Hygiene, Saarland University Medical Centre, Homburg/Saar, Germany.

Insights

Persistent diarrhea diagnosis in tropical settings is challenging. Multiplex PCR shows promise but requires confirmation for accurate pathogen identification, especially with high co-infection rates.

Area of Science:

  • Tropical medicine
  • Infectious diseases
  • Molecular diagnostics

Background:

  • Infectious diarrhoea is a major global health issue, particularly persistent cases (≥2 weeks).
  • Accurate pathogen identification is crucial for diagnosing persistent diarrhoea, but data from tropical regions are limited.
  • Stool-based PCR assays offer improved pathogen detection compared to traditional methods.

Purpose of the Study:

  • To investigate the spectrum of intestinal pathogens in patients with persistent diarrhoea and asymptomatic controls in southern Côte d'Ivoire.
  • To evaluate the utility of multiplex PCR in identifying a broad range of pathogens in a tropical setting.
  • To compare pathogen detection rates between patients and controls.

Main Methods:

  • A case-control study involving 68 patients with persistent diarrhoea and 68 asymptomatic controls.
  • Stool samples analyzed using Luminex(®) Gastrointestinal Pathogen Panel (GPP) multiplex PCR, microscopy, and rapid antigen detection tests.
  • Detection of bacteria, parasites, and viruses.

Main Results:

  • A broad spectrum of 20 different pathogens was detected, with at least one pathogen found in 84% of participants.
  • Co-infections were common, occurring in over 50% of participants.
  • Enterotoxigenic Escherichia coli (32%), Giardia intestinalis (29%), and Shigella species (20%) were predominant; Strongyloides stercoralis (10%) was the most prevalent helminth.

Conclusions:

  • Multiplex PCR assays are valuable screening tools for identifying intestinal pathogens in tropical settings.
  • Microscopy remains essential for detecting helminths and intestinal protozoa to ensure comprehensive etiological diagnosis.
  • Confirmation of positive PCR results is necessary to differentiate active infections from asymptomatic nucleic acid shedding.