Hybridization Screening of Very Short PCR Products for Paleoepidemiological Studies of Chagas’ Disease
Author(s) -
Michael Madden,
W.L. Salo,
John M. Streitz,
Arthur C. Aufderheide,
Gino Fornaciari,
Carlos Jaramillo,
Gustavo Adolfo Vallejo,
Roxana Yockteng,
Bernardo Arriaza,
F. Cárdenas-Arroyo,
Felipe Guhl
Publication year - 2001
Publication title -
biotechniques
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.617
H-Index - 131
eISSN - 1940-9818
pISSN - 0736-6205
DOI - 10.2144/01301st07
Subject(s) - kinetoplast , chagas disease , trypanosoma cruzi , biology , polymerase chain reaction , microbiology and biotechnology , dna , hybridization probe , cloning (programming) , kinetoplastida , virology , genetics , gene , parasite hosting , world wide web , computer science , programming language
Single strands of very short PCR products can be covalently immobilized to a slide and then easily detected by probe hybridization. In this work, the PCR product was a 70-nucleotide segment of ancient DNA, representing a portion of repeat mini-circle DNA from the kinetoplast of Trypanosoma cruzi, the infectious agent of Chagas' disease (American Trypanosomiasis). The target segment was initially established to be present in soft tissue samples taken from four "naturally" mummified Andean bodies using PCR followed by cloning and sequencing. Hybridization screening of the covalently immobilized PCR products positively identified products from 25 of 27 specimens of different tissues from these four mummies. The method appears to be ideal for the purpose of screening a large number of specimens when the target PCR product is very short.
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