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Comparison of stool collection and storage on Whatman FTA Elute cards versus frozen stool for enteropathogen
Tahaniyat Lalani1,2,3, Michele D Tisdale1,2,3, Jie Liu4
1Infectious Disease Clinical Research Program, Department of Preventive Medicine and Biostatistics, Uniformed Services University of the Health Sciences, Rockville, MD, United States of America.
Abstract:
The use of Polymerase Chain Reaction (PCR) assays for pathogen detection in travelers' diarrhea (TD) field studies is limited by the on-site processing and storage requirements for fecal specimens. The objectives of this investigation were to i) characterize the pathogen distribution in deployed military personnel with TD using the TaqMan® Array Card PCR (TAC) on frozen stool and diarrheal smears on Whatman FTA Elute cards (FTA cards), and to ii) compare TAC detection of enteropathogen targets using smeared FTA cards and frozen stool, using TAC on frozen stool as the 'reference standard'. Stool samples, obtained from active duty personnel with acute TD enrolled in a field trial, were smeared onto FTA cards and stored at room temperature. A corresponding aliquot of stool was frozen in a cryovial. FTA cards and frozen stool samples were tested at a central lab, using a customized TAC for detection of TD pathogens. 187 paired frozen stool samples and smeared FTA cards were stored for a median of 712 days (IQR 396-750) before testing. Overall detection rates were 78.6% for frozen stool and 73.2% for FTA cards. Diarrheagenic Escherichia coli were the most common bacteria identified. Using the TAC results on frozen stool as the reference, the overall sensitivity and specificity of TAC on FTA cards was 72.9% and 98.0% respectively. TAC on FTA cards demonstrated a decrease in sensitivity with increasing frozen stool quantification cycle (Cq) (90.0% in FTA cards with a corresponding frozen stool Cq < 30, and 72.9% in samples with a corresponding frozen stool Cq < 35). Our findings support the use and further development of FTA cards in combination with a quantitative PCR assay for enteropathogen detection in TD field studies.
Insights
Whatman FTA Elute cards offer a viable alternative for pathogen detection in travelers' diarrhea (TD) field studies. These cards, when used with Polymerase Chain Reaction (PCR) assays, show promising sensitivity and specificity for identifying enteropathogens.
Area of Science:
- Microbiology
- Molecular Biology
- Field Epidemiology
Background:
- Polymerase Chain Reaction (PCR) assays are crucial for pathogen detection in travelers' diarrhea (TD) studies.
- On-site processing and storage of fecal specimens pose significant challenges in field settings.
Purpose of the Study:
- To characterize pathogen distribution in military personnel with TD using PCR on frozen stool and FTA cards.
- To compare the efficacy of PCR detection on FTA cards versus frozen stool, with frozen stool as the reference standard.
Main Methods:
- Paired frozen stool and smeared FTA card samples from 187 military personnel with TD were analyzed.
- A customized TaqMan® Array Card PCR (TAC) assay was employed for enteropathogen detection.
- Samples were stored at room temperature (FTA cards) or frozen (stool) for a median of 712 days prior to testing.
Main Results:
- Overall detection rates were 78.6% for frozen stool and 73.2% for FTA cards.
- Diarrheagenic Escherichia coli was the most frequently identified pathogen.
- TAC on FTA cards demonstrated an overall sensitivity of 72.9% and specificity of 98.0% compared to frozen stool.
Conclusions:
- FTA cards are a suitable method for enteropathogen detection in TD field studies when combined with quantitative PCR.
- Further development of FTA card-based quantitative PCR assays is supported by these findings.
- FTA cards provide a stable, room-temperature storage solution for fecal specimens in field research.
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