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
Department of Medical Environmental Biology and Tropical Medicine, School of Medicine, Kangwon National University, Chuncheon 24341, Korea.
Department of Medical Research, Yangon, Republic of the Union of Myanmar.
Korean J Parasitol. 2016 Jun;54(3):253-9. doi: 10.3347/kjp.2016.54.3.253. Epub 2016 Jun 30.
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.
在(预)消除疟疾阶段,大多数以前的疟疾流行地区的疟疾患病率一直在下降。因此,在低传播环境中检测疟疾需要有效的、节省成本和时间的经过验证的混合策略。在本研究中,使用系统制备的已知密度样本评估最佳混合数量和最低检测限,随后进行基因组DNA提取和巢式PCR。由10个样本组成1个混合样本、每个样本20微升的混合策略是最佳的,恶性疟和间日疟感染时低至2个/微升的寄生虫密度足以检测出疟疾。这种混合方法在低传播环境(阳性率<9%)中处理大量样本时显示出有效性。结果表明,在DNA提取前对血样进行混合,然后进行常规巢式PCR,对于在低传播环境中筛查隐匿病例的疟疾检测是有用且有效的。