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A clinically authentic mouse model of enterovirus 71 (EV-A71)-induced neurogenic pulmonary oedema

机译:肠道病毒71(EV-A71)诱发的神经源性肺水肿的临床真实小鼠模型

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Enterovirus 71 (EV-A71) is a neurotropic virus that sporadically causes fatal neurologic illness among infected children. Animal models of EV-A71 infection exist, but they do not recapitulate in animals the spectrum of disease and pathology observed in fatal human cases. Specifically, neurogenic pulmonary oedema (NPE)-the main cause of EV-A71 infection-related mortality-is not observed in any of these models. This limits their utility in understanding viral pathogenesis of neurologic infections. We report the development of a mouse model of EV-A71 infection displaying NPE in severely affected animals. We inoculated one-week-old BALB/c mice with an adapted EV-A71 strain and identified clinical signs consistent with observations in human cases and other animal models. We also observed respiratory distress in some mice. At necropsy, we found their lungs to be heavier and incompletely collapsed compared to other mice. Serum levels of catecholamines and histopathology of lung and brain tissues of these mice strongly indicated onset of NPE. The localization of virally-induced brain lesions also suggested a potential pathogenic mechanism for EV-A71-induced NPE. This novel mouse model of virally-induced NPE represents a valuable resource for studying viral mechanisms of neuro-pathogenesis and pre-clinical testing of potential therapeutics and prophylactics against EV-A71-related neurologic complications.
机译:肠病毒71(EV-A71)是一种神经嗜性病毒,在感染的儿童中偶发性导致致命的神经系统疾病。存在EV-A71感染的动物模型,但它们并未在动物中概述在致命人类病例中观察到的疾病谱和病理学。具体而言,在任何这些模型中均未观察到神经源性肺水肿(NPE)-EV-A71感染相关死亡率的主要原因。这限制了它们在理解神经系统感染的病毒发病机理中的效用。我们报告在严重受影响的动物中显示NPE的EV-A71感染的小鼠模型的发展。我们给一星期大的BALB / c小鼠接种了适应性EV-A71株,并确定了与人类病例和其他动物模型中观察到的临床体征一致的临床体征。我们还观察到一些小鼠的呼吸窘迫。尸检时,我们发现它们的肺部较其他小鼠重且不完全塌陷。这些小鼠的血清儿茶酚胺水平和肺和脑组织的病理组织学强烈表明NPE的发作。病毒引起的脑损伤的定位也提示了EV-A71引起的NPE的潜在致病机制。这种新型的病毒诱导的NPE小鼠模型代表了宝贵的资源,可用于研究病毒的神经发病机理以及临床前测试针对EV-A71相关神经系统并发症的潜在疗法和预防方法。

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