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Detection and classification of Trypanosoma cruzi by DNA hybridization with nonradioactive probes.

作者信息

Solari A, Venegas J, Gonzalez E, Vasquez C

机构信息

Departamento de Bioquimica, Facultad de Medicina Norte, Universidad de Chile, Santiago.

出版信息

J Protozool. 1991 Nov-Dec;38(6):559-65. doi: 10.1111/j.1550-7408.1991.tb06080.x.

DOI:10.1111/j.1550-7408.1991.tb06080.x
PMID:1667933
Abstract

Total or kinetoplast DNA (kDNA) from 72 isolates and clones of Trypanosoma cruzi as well as from nine related trypanosomatids were analyzed by dot hybridization using nonradioactive kDNA or cloned minicircle fragments as probes. Biotinylated-kDNA probes generated by nick-translation proved reliable for distinguishing Zymodeme 1 and Zymodeme 2bol of T. cruzi parasites. In contrast, digoxigenin-labeled kDNA obtained by random-priming did not distinguish among T. cruzi isolates but did distinguish among New World leishmanias. Cloned minicircle fragments labeled with digoxigenin gave the same results as digoxigenin-labeled kDNA, except for a 10-fold decrease in sensitivity. Digoxigenin-labeled DNA probes proved useful in unambiguously detecting T. cruzi from different geographic regions of America. However, T. rangeli and T. cruzi marinkellei were not distinguished by these probes.

摘要

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1
Detection and classification of Trypanosoma cruzi by DNA hybridization with nonradioactive probes.
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