Wu Liang, Chen Sheng-Xia, Jiang Xu-Gan, Cao Jian-Ping
School of Medical Technology, Jiangsu University, Zhenjiang, People's Republic of China.
Exp Parasitol. 2009 Dec;123(4):384-7. doi: 10.1016/j.exppara.2009.08.013. Epub 2009 Aug 29.
A Real-time quantitative PCR assay to quantify the Toxoplasma gondii apicoplast was studied. Primers were designed to amplify a 305bp product specific to T. gondii apicoplast. Standard curves were generated for both T. gondii apicoplast DNA and genomic DNA, and were used to compute the relative concentration of apicoplast DNA copies in the test samples. The results indicated that the copies of T. gondii apicoplast DNA was significantly low when exposed to ciprofloxacin, clindamycin and azithromycin for 48h in the second infectious cycle. Our study shows that the Real-time PCR technique is a simple and quick technique for screening the anti-apicoplast drugs.
研究了一种用于定量弓形虫顶质体的实时定量PCR检测方法。设计引物以扩增特定于弓形虫顶质体的305bp产物。为弓形虫顶质体DNA和基因组DNA均生成了标准曲线,并用于计算测试样品中顶质体DNA拷贝的相对浓度。结果表明,在第二个感染周期中,当暴露于环丙沙星、克林霉素和阿奇霉素48小时时,弓形虫顶质体DNA的拷贝数显著降低。我们的研究表明,实时PCR技术是一种筛选抗顶质体药物的简单快速技术。