Simple lateral flow assays for microbial detection in stool
Related Experiment Video
Updated: Jan 23, 2026

Detection and Genogrouping of Noroviruses from Children's Stools By Taqman One-step RT-PCR
Published on: July 22, 2012
Wendy A Henderson1, Lichen Xiang1,2, Nicolaas H Fourie1
1Division of Intramural Research , National Institute of Nursing Research , National Institutes of Health , Department of Health and Human Services , Bethesda , MD 20892 , USA .
Abstract:
Diarrheal diseases claim the lives of 1300 children daily, mostly in the developing world. We have developed a simple lateral flow assay capable of detecting E. coli and EPEC DNA and RNA rapidly (<15 minutes) at the point-of-need, directly from stool without nucleic acid extraction or molecular amplification. The limit of detection of the method is 1 nM using synthetic DNA target substrates spiked into stool. However, due to the endogenous amplification of the 23S rRNA targets, we were able to detect the endogenous EPEC in pea-sized (5 mg) stool without labor-intensive and time-consuming nucleic acid purification or target amplification using enzymes. The significance of this method is that it is rapid (<15 minutes) and simple (without nucleic acid purification or molecular amplification) and does not require instrumentation, or access to a laboratory, cold chain or electric power. Thus, it is well-suited for point-of-need use in remote and/or resource-limited settings in the developing world where the mortality due to diarrheal diseases is especially high. The rapid testing of stool pathogens in real time at the point-of-need will decrease the loss of patients to follow-up, and enable patients to be treated earlier with the appropriate therapeutics in both the developed and developing world settings.
Related Concept Videos
Serum Laboratory Studies, Stool Test, Breath Test
Lateralization
Microbial Morphologies
Microbial Fermentation
Microbial Nutrition
Microbial Classification System

