| Literature DB >> 16054487 |
Andrew Cox1, Aimee Tilley, Francis McOdimba, Jenna Fyfe, Mark Eisler, Geoff Hide, Susan Welburn.
Abstract
Direct PCR analysis of trypanosome infected blood samples in the quantities required for large scale epidemiological study has always been problematic. Current methods for identifying and differentiating trypanosomes typically require several species-specific reactions, many of which rely on mouse passaged samples to obtain quality concentrated genomic DNA. As a consequence important epidemiological information may be lost during the sample preparation stage. Here, we report a PCR methodology that reduces processing and improves on the sensitivity of present screening methods. The PCR technique targets the gene encoding the small ribosomal subunit in order to identify and differentiate all clinically important African trypanosome species and some subspecies. The method is more economical, simple, and sensitive than current screening methods, and yields more detailed information, thereby making it a viable tool for large-scale epidemiological studies.Entities:
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Year: 2005 PMID: 16054487 DOI: 10.1016/j.exppara.2005.03.014
Source DB: PubMed Journal: Exp Parasitol ISSN: 0014-4894 Impact factor: 2.011