Biomedical Primate Research Centre, Department of Parasitology, Rijswijk, The Netherlands.
PLoS One. 2013;8(1):e54888. doi: 10.1371/journal.pone.0054888. Epub 2013 Jan 24.
A major challenge for strategies to combat the human malaria parasite Plasmodium vivax is the presence of hypnozoites in the liver. These dormant forms can cause renewed clinical disease after reactivation through unknown mechanisms. The closely related non-human primate malaria P. cynomolgi is a frequently used model for studying hypnozoite-induced relapses. Here we report the generation of the first transgenic P. cynomolgi parasites that stably express fluorescent markers in liver stages by transfection with novel DNA-constructs containing a P. cynomolgi centromere. Analysis of fluorescent liver stages in culture identified, in addition to developing liver-schizonts, uninucleate persisting parasites that were atovaquone resistant but primaquine sensitive, features associated with hypnozoites. We demonstrate that these hypnozoite-forms could be isolated by fluorescence-activated cell sorting. The fluorescently-tagged parasites in combination with FACS-purification open new avenues for a wide range of studies for analysing hypnozoite biology and reactivation.
一个主要的挑战,对于策略来对抗人类疟原虫恶性疟原虫是存在的休眠子在肝脏。这些休眠形式可以引起重新激活后的临床疾病通过未知的机制。密切相关的非人类灵长类动物疟原虫 P. cynomolgi 是一种常用的模型来研究休眠子诱导的复发。在这里,我们报告了第一代的转基因恶性疟原虫寄生虫稳定表达荧光标记的肝脏阶段通过转染含有一个恶性疟原虫着丝粒的新型 DNA 构建体。分析荧光肝脏阶段在文化中确定,除了发育中的肝裂殖体,单核持久寄生虫是阿托伐醌耐药但伯氨喹敏感,特征与休眠子相关。我们证明这些休眠子形式可以通过荧光激活细胞分选分离。荧光标记的寄生虫与 FACS 纯化相结合,为分析休眠子生物学和激活开辟了新的途径。