PCR-based identification of Trypanosoma lewisi and Trypanosoma musculi using maxicircle kinetoplast DNA

被引:11
|
作者
Hong, Xiao-Kun [1 ]
Zhang, Xuan [1 ]
Alejandro Fusco, Octavio [2 ]
Lan, You-Gen [1 ]
Lun, Zhao-Rong [1 ]
Lai, De-Hua [1 ]
机构
[1] Sun Yat Sen Univ, Sch Life Sci, State Key Lab Biocontrol, Ctr Parasit Organisms, Guangzhou 510275, Guangdong, Peoples R China
[2] Minist Salud, ANLIS Carlos G Malbran, Inst Nacl Parasitol, RA-1063 Buenos Aires, DF, Argentina
关键词
Morphology; Maxicircle kinetoplast DNA; Trypanosoma lewisi; Trypanosoma musculi; HUMAN PATHOGEN; HERPETOSOMA; INFECTION; DIAGNOSIS; INFANT; CRUZI; SEQUENCES; BRUCEI;
D O I
10.1016/j.actatropica.2017.04.007
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
Trypanosoma lewisi, transmitted by rat fleas, is a widespread pathogen specific to rats with records of human infection cases. Its closely related species with global distribution, Trypanosoma musculi, is transmitted between mice by ingestion of infected fleas. These trypanosomes are of similar morphology, making it difficult to distinguish them by microscopy. In this study, we have developed a rapid, sensitive and reliable PCR method for the diagnosis of T. lewisi and T. musculi. The T. lewisi-specific amplicons were not produced by other Trypanosoma, such as T. musculi, T. brucei complex or T. cruzi, neither by an outgroup of Leishmania amazonensis. The detection limits of the three pairs of T. lewisi-specific primers were 50 ng, 1 ng and 10 ng of total DNA, respectively. The primers designed for T. musculi primers showed specifically that amplicon strictly in T. musculi and their detection limits were 10 ng and 1 ng of total DNA. To simplify the detection process, we managed to apply our method directly on tail blood samples without complicated DNA purification. In conclusion, PCR with our primers could be a highly sensitive, specific protocol to detect and distinguish T. lewisi and T. musculi from other trypanosomes.
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页码:207 / 212
页数:6
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