| Literature DB >> 30576752 |
Yunyun Geng1, Guanhui Liu2, Libing Liu3, Qiaoen Deng4, Liwei Zhao5, Xiao Xia Sun3, Jinfeng Wang3, Baohua Zhao6, Jianchang Wang7.
Abstract
Campylobacter jejuni (C. jejuni), a foodborne pathogen, is a major contributor to human bacterial gastroenteritis worldwide and detrimental to public health. It is crucial for initiating appropriate outbreak control strategies to rapidly detect C. jejuni. As a novel isothermal gene amplification technique, recombinase polymerase amplification (RPA) has been developed for the molecular detection of diverse pathogens. In this study, we developed a real-time RPA assay so as to achieve the rapid and efficient detection of C. jejuni by targeting the hipO gene. The specificity and senstivity of real-time RPA was validated and the practical applicability of the method for the detection of C. jejuni in artificially contaminated milk and chicken breast samples was proved by comparing their reaction time, sensitivity, and efficacy with those of real-time PCR and culture-based methods. Based on the real-time RPA assay, analysis time was reduced to approximately 13 mins from 60 mins and the results were as reliable as those of the real-time PCR assay. Taken together, in terms of the detection of C. jejuni, the real-time RPA method was simple, rapid, sensitive, and reliable.Entities:
Keywords: Campylobacter jejuni; Rapid detection; Real-time RPA; hipO
Mesh:
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Year: 2018 PMID: 30576752 DOI: 10.1016/j.mimet.2018.12.017
Source DB: PubMed Journal: J Microbiol Methods ISSN: 0167-7012 Impact factor: 2.363