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Differential tissular distribution of Litomosoides sigmodontis microfilariae between microfilaremic and amicrofilaremic mice following experimental infection

机译:实验感染后微丝线虫和小丝线虫小鼠之间丝状线虫微丝aria的差异性组织分布

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Filariases are caused by onchocercid nematodes that are transmitted by arthropod vectors. More than 180 million people are infected worldwide. Mass drug administration has been set up in many endemic areas to control the parasite burden. Although very successful in limiting microfilarial load, transmission has not been completely interrupted in such areas. A proportion of infected patients with lymphatic filariasis or loiasis are known to be amicrofilaremic, as they do not present microfilariae in their bloodstream despite the presence of adult worms. A mirror status also exists in CBA/Ca mice infected with Litomosoides sigmodontis, the well-established model of filariasis. Using this model, the goal of this study was to determine if the kinetics of blood clearance of microfilariae differed between amicrofilaremic CBA/Ca mice and microfilaremic BALB/c mice. For this purpose, a qPCR approach was devised to detect microfilariae in different tissues, after a controlled inoculation of microfilariae. We showed that the rapid clearance of microfilariae from the pleural cavity or from the bloodstream of CBA/Ca mice was associated with a massive accumulation of first stage larvae in the lungs, liver and spleen.
机译:丝虫病是由节肢动物载体传播的盘尾线虫引起的。全球有超过1.8亿人被感染。已经在许多流行地区建立了大规模药物管理,以控制寄生虫负担。尽管在限制微丝负载方面非常成功,但是在这些区域中传输尚未完全中断。已知有一部分感染的淋巴丝虫病或精神病患者是微丝虫病,因为尽管有成虫,他们的血流中也没有微丝虫病。在感染了丝虫病(成熟的丝虫病模型)的CBA / Ca小鼠中也存在镜像状态。使用该模型,本研究的目的是确定微丝虫病的CBA / Ca小鼠和微丝虫病的BALB / c小鼠之间的微丝虫的血液清除动力学是否不同。为了这个目的,设计了qPCR方法以在控制接种微丝aria后检测不同组织中的微丝aria。我们表明,从胸膜腔或CBA / Ca小鼠血流中快速清除微丝aria与肺,肝和脾中大量第一阶段幼虫的积累有关。

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