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Updated: Jan 22, 2026

Development and Testing of Species-specific Quantitative PCR Assays for Environmental DNA Applications
Published on: November 5, 2020
Development of a specific cytolethal distending toxin (cdt) gene (Eacdt)-based PCR assay for the detection of
Atsushi Hinenoya1, Hidetoshi Ichimura2, Noritomo Yasuda3
1School of Life and Environmental Sciences, Osaka Prefecture University, 1-58, Rinku ourai-kita, Izumisano, Osaka 598-8531, Japan; Graduate School of Life and Environmental Sciences, Osaka Prefecture University, Osaka, Japan.
Abstract:
Many Escherichia albertii isolates, an emerging pathogen of human and birds, might have been misidentified due to the difficulty of differentiating this bacterium from Escherichia coli and Shigella spp. by routine biochemical tests, resulting in underestimation of E. albertii infections. We have developed a polymerase chain reaction (PCR) assay that targets E. albertii cytolethal distending toxin (Eacdt) genes, which include the genes previously identified as Escherichia coli cdt-II. This assay could generate a single 449-bp PCR product in each of 67 confirmed E. albertii strains but failed to produce PCR product from any of the tested non-E. albertii enteric strains belonging to 37 different species, indicating 100% sensitivity and specificity of the PCR assay. The detection limit was 10 CFU per PCR tube and could detect 105 CFU E. albertii per gram of spiked healthy human stool. The Eacdt gene-based PCR could be useful for simple, rapid, and accurate detection and identification of E. albertii.
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