Paziewska-Harris A, Schoone G, Schallig H D F H
Royal Tropical Institute, Parasitology Unit, KIT Biomedical Research, Meibergdreef 39, 1105 AZ, Amsterdam, The Netherlands.
Parasitol Res. 2016 Jul;115(7):2873-7. doi: 10.1007/s00436-016-5044-z. Epub 2016 Apr 20.
Viability estimation of the highly resistant oocysts of Cryptosporidium remains a key issue for the monitoring and control of this pathogen. We present here a simple 'one tube' quantitative PCR (qPCR) protocol for viability estimation using a DNA extraction protocol which preferentially solubilizes excysted sporozoites rather than oocysts. Parasite DNA released from excysted sporozoites was quantified by real-time qPCR using a ribosomal DNA marker. The qPCR signal was directly proportional to the number of oocysts excysted, and a power-law relationship was noted between oocyst age and the proportion excysting. Unexcysted oocysts released negligible amounts of DNA making the method suitable for estimating viability of as few as 10 oocysts.
隐孢子虫高度抗性卵囊的活力评估仍然是监测和控制这种病原体的关键问题。我们在此展示一种简单的“单管”定量PCR(qPCR)方案,用于活力评估,该方案使用一种优先溶解脱囊子孢子而非卵囊的DNA提取方案。使用核糖体DNA标记,通过实时qPCR对脱囊子孢子释放的寄生虫DNA进行定量。qPCR信号与脱囊卵囊的数量直接成正比,并且在卵囊年龄与脱囊比例之间发现了幂律关系。未脱囊的卵囊释放的DNA量可忽略不计,这使得该方法适用于评估低至10个卵囊的活力。