| Literature DB >> 31272742 |
Atsushi Hinenoya1, Hidetoshi Ichimura2, Noritomo Yasuda3, Seiya Harada4, Kazuhiro Yamada5, Masahiro Suzuki5, Yoshio Iijima6, Akira Nagita7, M John Albert8, Noritoshi Hatanaka3, Sharda Prasad Awasthi3, Shinji Yamasaki9.
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.Entities:
Keywords: Cytolethal distending toxin; E. albertii; PCR; cdt
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Year: 2019 PMID: 31272742 DOI: 10.1016/j.diagmicrobio.2019.04.018
Source DB: PubMed Journal: Diagn Microbiol Infect Dis ISSN: 0732-8893 Impact factor: 2.803