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Detection and Classification of Trypanosoma cruzi by DNA Hybridization with Nonradioactive Probes
Author(s) -
SOLARI A.,
VENEGAS J.,
GONZALEZ E.,
VASQUEZ C.
Publication year - 1991
Publication title -
the journal of protozoology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.067
H-Index - 77
eISSN - 1550-7408
pISSN - 0022-3921
DOI - 10.1111/j.1550-7408.1991.tb06080.x
Subject(s) - trypanosoma cruzi , hybridization probe , dna , dna–dna hybridization , biology , in situ hybridization , microbiology and biotechnology , computational biology , genetics , gene , parasite hosting , computer science , gene expression , world wide web
. 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.