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Detection and Genogrouping of Noroviruses from Children's Stools By Taqman One-step RT-PCR
Published on: July 22, 2012
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.
Abstract:
Infectious diarrhoea ranks among the leading causes of morbidity worldwide. Although most acute diarrhoeal episodes are self-limiting, the diagnosis and treatment of persistent diarrhoea (≥2 weeks) are cumbersome and require laboratory identification of the causative pathogen. Stool-based PCR assays have greatly improved the previously disappointing pathogen detection rates in high-income countries, but there is a paucity of quality data from tropical settings. We performed a case-control study to elucidate the spectrum of intestinal pathogens in patients with persistent diarrhoea and asymptomatic controls in southern Côte d'Ivoire. Stool samples from 68 patients and 68 controls were obtained and subjected to molecular multiplex testing with the Luminex(®) Gastrointestinal Pathogen Panel (GPP), microscopy and rapid antigen detection tests for the diagnosis of diarrhoeagenic pathogens. Overall, 20 different bacteria, parasites and viruses were detected by the suite of diagnostic methods employed. At least one pathogen was observed in 84% of the participants, and co-infections were observed in >50% of the participants. Enterotoxigenic Escherichia coli (32%), Giardia intestinalis (29%) and Shigella species (20%) were the predominant pathogens, and Strongyloides stercoralis (10%) was the most prevalent helminth. Pathogen frequencies and numbers of co-infections were similar in patients and controls. Although the Luminex(®) GPP detects a broad range of pathogens, microscopy for helminths and intestinal protozoa remains necessary to cover the full aetiological spectrum in tropical settings. We conclude that highly sensitive multiplex PCR assays constitute a useful screening tool, but that positive results might need to be confirmed by independent methods to discriminate active infection from asymptomatic faecal shedding of nucleic acids.
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.

