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Development of a TaqMan based real-time PCR assay for detection of Clonorchis sinensis DNA in human stool samples and fishes
Authors:Cai Xian-Quan  Yu Hai-Qiong  Bai Jian-Shan  Tang Jian-Dong  Hu Xu-Chu  Chen Ding-Hu  Zhang Ren-Li  Chen Mu-Xin  Ai Lin  Zhu Xing-Quan
Institution:
  • a State Key Laboratory of Veterinary Etiological Biology, Key Laboratory of Veterinary Parasitology of Gansu Province, Lanzhou Veterinary Research Institute, CAAS, Lanzhou, Gansu Province 730046, China
  • b Zhongshan Entry-Exit Inspection and Quarantine Bureau, Zhongshan, Guangdong Province 528403, China
  • c College of Veterinary Medicine, South China Agricultural University, Guangzhou, Guangdong Province 510642, China
  • d Technical Center, Guangdong Entry-Exit Inspection and Quarantine Bureau, Guangzhou, Guangdong Province 510630, China
  • e Guangzhou Airport Entry-Exit Inspection and Quarantine Bureau, Guangzhou, Guangdong Province 510470, China
  • f Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, Guangdong Province 510089, China
  • g Shenzhen Center for Disease Control and Prevention, Shenzhen, Guangdong Province 518020, China
  • h National Institute of Parasitic Diseases, Chinese Center for Disease Control and Prevention, Shanghai 200025, China
  • i College of Animal Science and Technology, Yunnan Agricultural University, Kunming, Yunnan Province 650201, China
  • Abstract:Clonorchiasis caused by the oriental liver fluke Clonorchis sinensis is a fish-borne zoonosis endemic in a number of countries. This article describes the development of a TaqMan based real-time PCR assay for detection of C. sinensis DNA in human feces and in fishes. Primers targeting the first internal transcribed spacer (ITS-1) sequence of the fluke were highly specific for C. sinensis, as evidenced by the negative amplification of closely related trematodes in the test with the exception of Opisthorchis viverrini. The detection limit of the assay was 1 pg of purified genomic DNA, 5 EPG (eggs per gram feces) or one metacercaria per gram fish filet. The assay was evaluated by testing 22 human fecal samples and 37 fish tissues microscopically determined beforehand, and the PCR results were highly in agreement with the microscopic results. This real-time PCR assay provides a useful tool for the sensitive detection of C. sinensis DNA in human stool and aquatic samples in China and other endemic countries where O. viverrini and Opisthorchis felineus are absent.
    Keywords:Clonorchis sinensis  Clonorchiasis  TaqMan probe  Real-time PCR  Fish  Human stool  Detection
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