| Literature DB >> 12965903 |
Miguel Angel Chiurillo1, Gladys Crisante, Agustina Rojas, Andreina Peralta, Manuel Dias, Palmira Guevara, Néstor Añez, José Luis Ramírez.
Abstract
We used the species specificity and repetitious nature of subtelomeric kinetoplastida sequences to generate a duplex PCR assay for the simultaneous detection of Trypanosoma cruzi and Trypanosoma rangeli in experimentally and naturally infected triatomine (Reduviid) bugs and in infected human subjects. The assay was species specific and was capable of detecting 1/20th of T. cruzi and 1/4th of T. rangeli cell equivalents without complementary hybridization. In addition, the PCR-based assay was robust enough for direct application to difficult biological samples such as Reduviid feces or guts and was capable of recognizing all T. cruzi and T. rangeli strains and lineages. Because the assay primers amplify entirely different target sequences, no reaction interference was observed, facilitating future adaptation of this assay to an automated format.Entities:
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Year: 2003 PMID: 12965903 PMCID: PMC193880 DOI: 10.1128/cdli.10.5.775-779.2003
Source DB: PubMed Journal: Clin Diagn Lab Immunol ISSN: 1071-412X