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Optimization of DNA Extraction from Individual Sand Flies for PCR Amplification

2019; Multidisciplinary Digital Publishing Institute; Volume: 2; Issue: 2 Linguagem: Inglês

10.3390/mps2020036

2409-9279

Lorena G. Caligiuri, Adolfo E. Sandoval, José Carlos Miranda, Felipe Arley Costa Pessoa, María Soledad Santini, Oscar Daniel Salomón, Nágila Francinete Costa Secundino, Christina B. McCarthy,

Trypanosoma species research and implications

Numerous protocols have been published for extracting DNA from phlebotomines. Nevertheless, their small size is generally an issue in terms of yield, efficiency, and purity, for large-scale individual sand fly DNA extractions when using traditional methods. Even though this can be circumvented with commercial kits, these are generally cost-prohibitive for developing countries. We encountered these limitations when analyzing field-collected Lutzomyia spp. by polymerase chain reaction (PCR) and, for this reason, we evaluated various modifications on a previously published protocol, the most significant of which was a different lysis buffer that contained Ca2+ (buffer TESCa). This ion protects proteinase K against autolysis, increases its thermal stability, and could have a regulatory function for its substrate-binding site. Individual sand fly DNA extraction success was confirmed by amplification reactions using internal control primers that amplify a fragment of the cacophony gene. To the best of our knowledge, this is the first time a lysis buffer containing Ca2+ has been reported for the extraction of DNA from sand flies.