Key result
MDA boosts trypanosome detection sensitivity and PCR capacity 20-fold over nested PCR.
Why the study?
Trypanosome infections have low parasitemias, limiting DNA template availability for detection and genotyping, necessitating improved amplification methods.
Effect estimate: 20-fold increase
MDA significantly increases the sensitivity and utility of limited DNA samples for detecting and genotyping Trypanosoma species.
MDA boosts trypanosome detection from limited samples in animals; leaves open human diagnostic validation.
Whole genome amplification methods are a recently developed tool for amplifying DNA from limited template. We report its application in trypanosome infections, characterized by low parasitemias. Multiple displacement amplification (MDA) amplifies DNA with a simple in vitro step and was evaluated on mouse blood samples on FTA filter cards with known numbers of Trypanosoma brucei parasites. The data showed a 20-fold increase in the number of PCRs possible per sample, using primers diagnostic for the multicopy ribosomal ITS region or 177-bp repeats, and a 20-fold increase in sensitivity over nested PCR against a single-copy microsatellite. Using MDA for microsatellite genotyping caused allele dropout at low DNA concentrations, which was overcome by pooling multiple MDA reactions. The validity of using MDA was established with samples from Human African Trypanosomiasis patients. The use of MDA allows maximal use of finite DNA samples and may prove a valuable tool in studies where multiple reactions are necessary, such as population genetic analyses.
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Morrison et al. (2007) studied Trypanosome infections. Multiple displacement amplification (MDA) vs. Nested PCR was evaluated on Number of PCRs possible per sample and sensitivity (20-fold increase). Multiple displacement amplification (MDA) provided a 20-fold increase in the number of PCRs possible per sample and a 20-fold increase in sensitivity over nested PCR for trypanosome detection.
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