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Updated: Aug 29, 2026

Guided Protocol for Fecal Microbial Characterization by 16S rRNA-Amplicon Sequencing
Published on: March 19, 2018
Direct amplification and genotyping of Dientamoeba fragilis from human stool specimens
Ron Peek1, Freek R Reedeker, Tom van Gool
1Department of Medical Microbiology, Tropical Medicine and AIDS, University of Amsterdam, Amsterdam, The Netherlands. r.peek@amc.uva.nl
Abstract:
Dientamoeba fragilis is a globally occurring parasite that has been recognized as a causative agent of gastrointestinal symptoms. A single-round PCR was developed to detect D. fragilis DNA directly from human stool samples. The genetic diversity of D. fragilis from 93 patients and 6 asymptomatic carriers was examined by PCR followed by restriction fragment length polymorphism and sequencing of part of the small-subunit rRNA gene. The data show that D. fragilis sequences can be studied directly from fecal specimens despite the absence of a cyst stage and without the need for prior culturing. In addition, the results suggest strongly that D. fragilis shows remarkably little variation in its small-subunit rRNA gene.

