Enteropathogens in paediatric gastroenteritis: comparison of routine diagnostic and molecular methods

A Tilmanne1, D Martiny2, C Quach3

  • 1Division of Infection Prevention and Control, Hôpital Universitaire des Enfants Reine Fabiola, Brussels, Belgium; Divisions of Pediatric Infectious Diseases and Medical Microbiology, CHU Sainte Justine, Montreal, Quebec, Canada.

Insights

Molecular diagnostic tools for acute gastroenteritis (AGE) show high positivity but interpretation challenges persist. Routine methods still detect pathogens missed by molecular assays, questioning the clinical utility of newer techniques.

Area of Science:

  • Clinical microbiology
  • Molecular diagnostics
  • Pediatric infectious diseases

Background:

  • Acute gastroenteritis (AGE) diagnosis lacks sensitive and specific routine methods.
  • Molecular diagnostic techniques are increasingly adopted but their clinical significance is debated.
  • Interpreting positive molecular results in both symptomatic and asymptomatic individuals is challenging.

Purpose of the Study:

  • To compare the diagnostic performance of routine methods and molecular methods for detecting enteropathogens in children with AGE.
  • To evaluate the clinical significance of positive results from molecular assays versus traditional methods.
  • To assess pathogen detection rates in symptomatic children and asymptomatic controls.

Main Methods:

  • Prospective recruitment of pediatric patients with AGE and asymptomatic controls from university hospitals.
  • Stool sample analysis using routine methods (culture, immunochromatography, microscopy) and a multiplex PCR assay (Luminex Gastrointestinal Pathogen Panel).
  • Comparison of pathogen detection rates between Luminex assay and routine diagnostic methods.

Main Results:

  • Enteropathogens were detected in 62.4% of AGE cases and 29.1% of controls when combining both methods.
  • Luminex detected pathogens like Salmonella more frequently than routine methods (16.3% vs. 3.9%, p < 0.05).
  • Routine methods identified pathogens (e.g., Campylobacter, Shigella, Yersinia) missed by the Luminex assay.

Conclusions:

  • Molecular tools offer high positivity and rapid results for AGE diagnosis.
  • High detection rates in both cases and controls complicate result interpretation.
  • The clinical value of molecular techniques is questioned due to missed pathogens and interpretation difficulties.
Abstract

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