Real-time recombinase polymerase amplification assay for the rapid and sensitive detection of Campylobacter jejuni in food samples

被引:33
|
作者
Geng, Yunyun [1 ,2 ]
Liu, Guanhui [3 ]
Liu, Libing [4 ,5 ]
Deng, Qiaoen [6 ]
Zhao, Liwei [1 ]
Sun, Xiao Xia [4 ,5 ]
Wang, Jinfeng [4 ,5 ]
Zhao, Baohua [2 ]
Wang, Jianchang [4 ,5 ]
机构
[1] Hebei Univ Chinese Med, Dept Pharmacol, 326 South Xinshi Rd, Shijiazhuang 050200, Hebei, Peoples R China
[2] Hebei Normal Univ, Coll Life Sci, 20,Rd E 2nd Ring South, Shijiazhuang 050024, Hebei, Peoples R China
[3] Hebei Univ Engn, Coll Life Sci & Food Engn, 178 Zhonghua South St, Handan 056038, Hebei, Peoples R China
[4] Hebei Entry Exit Inspect & Quarantine Bur, Ctr Inspect & Quarantine, 318 Hepingxilu Rd, Shijiazhuang 050051, Hebei, Peoples R China
[5] Hebei Acad Inspect & Quarantine Sci & Technol, 318 Hepingxilu Rd, Shijiazhuang 050051, Hebei, Peoples R China
[6] Eighth Hosp Shjiazhuang, 620 Xinhua Rd, Shijiazhuang 050081, Hebei, Peoples R China
关键词
Campylobacter jejuni; hipO; Real-time RPA; Rapid detection; COLI; SPP; PCR; DIFFERENTIATION; EPIDEMIOLOGY; CONSUMPTION; SALMONELLA; INFECTIONS; POULTRY; CATTLE;
D O I
10.1016/j.mimet.2018.12.017
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:31 / 36
页数:6
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