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Effective High-Throughput Blood Pooling Strategy before DNA Extraction for Detection of Malaria in Low-Transmission Settings

In the era of (pre) elimination setting, the prevalence of malaria has been decreasing in most of the previously endemic areas. Therefore, effective cost- and time-saving validated pooling strategy is needed for detection of malaria in low transmission settings. In this study, optimal pooling number...

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Detalles Bibliográficos
Autores principales: Nyunt, Myat Htut, Kyaw, Myat Phone, Thant, Kyaw Zin, Shein, Thinzer, Han, Soe Soe, Zaw, Ni Ni, Han, Jin-Hee, Lee, Seong-Kyun, Muh, Fauzi, Kim, Jung-Yeon, Cho, Shin-Hyeong, Lee, Sang-Eun, Yang, Eun-Jeong, Chang, Chulhun L., Han, Eun-Taek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Parasitology and Tropical Medicine 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4977795/
https://www.ncbi.nlm.nih.gov/pubmed/27417078
http://dx.doi.org/10.3347/kjp.2016.54.3.253
Descripción
Sumario:In the era of (pre) elimination setting, the prevalence of malaria has been decreasing in most of the previously endemic areas. Therefore, effective cost- and time-saving validated pooling strategy is needed for detection of malaria in low transmission settings. In this study, optimal pooling numbers and lowest detection limit were assessed using known density samples prepared systematically, followed by genomic DNA extraction and nested PCR. Pooling strategy that composed of 10 samples in 1 pool, 20 µl in 1 sample, was optimal, and the parasite density as low as 2 p/µl for both falciparum and vivax infection was enough for detection of malaria. This pooling method showed effectiveness for handling of a huge number of samples in low transmission settings (<9% positive rate). The results indicated that pooling of the blood samples before DNA extraction followed by usual nested PCR is useful and effective for detection of malaria in screening of hidden cases in low-transmission settings.