Carnevale Silvana, Velásquez Jorge N, Portillo Hernando Del, Labbé Jorge H, Cabrera Marta G, Ferella Marcela, Andersson Björn, Guarnera Eduardo A, Angel Sergio O
Departamento de Parasitología, Instituto Nacional de Enfermedades Infecciosas, ANLIS "Dr. Carlos G. Malbrán," Ciudad de Buenos Aires, Argentina.
Exp Parasitol. 2004 Nov-Dec;108(3-4):81-8. doi: 10.1016/j.exppara.2004.07.012.
We cloned and characterized a Plasmodium vivax repeat element of 7872bp named PvRE7.8. Several internal tandem repeats were found along the sequence. The repetitive nature of the PvRE7.8 element was confirmed by hybridization of a P. vivax YAC library. Based on the data bank analysis and the presence of two contiguous putative genes that may encode proteins related to DNA metabolism, PvRE7.8 could be considered an inactivated transposon-LINE element. By using Pv79 as probe or primers derived from Pv79-flanking sequences, P. vivax DNA Could be detected from whole blood and mosquito samples. We consider that the repeat element described here has potential for P. vivax malaria diagnosis and for epidemiological analysis of P. vivax transmission areas.
我们克隆并鉴定了一个名为PvRE7.8的7872bp间日疟原虫重复元件。沿着该序列发现了几个内部串联重复序列。通过间日疟原虫酵母人工染色体文库的杂交证实了PvRE7.8元件的重复性质。基于数据库分析以及存在两个可能编码与DNA代谢相关蛋白质的相邻推定基因,PvRE7.8可被视为一个失活的转座子-长散在核元件。通过使用Pv79作为探针或源自Pv79侧翼序列的引物,可从全血和蚊子样本中检测到间日疟原虫DNA。我们认为这里描述的重复元件在间日疟原虫疟疾诊断和间日疟原虫传播地区的流行病学分析方面具有潜力。