Sensitive and rapid detection of Clonorchis sinensis infection in fish by loop-mediated isothermal amplification (LAMP)

被引:71
作者
Cai, X. Q. [1 ,2 ]
Xu, M. J. [1 ]
Wang, Y. H. [2 ]
Qiu, D. Y. [2 ]
Liu, G. X. [2 ]
Lin, A. [1 ]
Tang, J. D. [1 ]
Zhang, R. L. [4 ]
Zhu, X. Q. [1 ,3 ]
机构
[1] S China Agr Univ, Coll Vet Med, Guangzhou 510642, Guangdong, Peoples R China
[2] Zhongshan Entry Exit Inspect & Quarantine Bur, Zhongshan 528403, Guangdong Prov, Peoples R China
[3] CAAS, State Key Lab Vet Etiol Biol, Key Lab Vet Parasitol Gansu Prov, Lanzhou Vet Res Inst, Lanzhou 730046, Gansu Province, Peoples R China
[4] Shenzhen Ctr Dis Control & Prevent, Mol Biol Lab, Shenzhen 518020, Guangdong Prov, Peoples R China
关键词
PCR;
D O I
10.1007/s00436-010-1812-3
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
The fish-borne clonorchiasis caused by the oriental liver fluke Clonorchis sinensis is endemic in a number of countries with over 35 million people being infected globally. Rapid and accurate detection of C. sinensis in its intermediate host fish is important for the control and prevention of clonorchiasis in areas where the disease is endemic. In the present study, we established a loop-mediated isothermal amplification (LAMP) approach for the sensitive and rapid detection of C. sinensis metacercariae in fish. The specificity and sensitivity of primers designed from the C. sinensis cathepsins B3 gene were evaluated, and specific amplification products were obtained with C. sinensis, while no amplification products were detected with DNA of related trematodes, demonstrating the specificity of the assay. The LAMP assay was proved to be 100 times more sensitive than a conventional polymerase chain reaction for detection of C. sinensis. The established LAMP assay provides a useful tool for the rapid and sensitive detection of C. sinensis in fish, which has important implications for the effective control of human clonorchiasis.
引用
收藏
页码:1379 / 1383
页数:5
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