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Increased Viral Dissemination in the Brain and Lethality in MCMV-Infected Dicer-Deficient Neonates

机译:MCMV感染切丁机缺陷的新生儿大脑中和致命性中病毒传播的增加。

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摘要

Among Herpesviruses, Human Cytomegalovirus (HCMV or HHV-5) represents a major threat during congenital or neonatal infections, which may lead to encephalitis with serious neurological consequences. However, as opposed to other less prevalent pathogens, the mechanisms and genetic susceptibility factors for CMV encephalitis are poorly understood. This lack of information considerably reduces the prognostic and/or therapeutic possibilities. To easily monitor the effects of genetic defects on brain dissemination following CMV infection we used a recently developed in vivo mouse model based on the neonatal inoculation of a MCMV genetically engineered to express Luciferase. Here, we further validate this protocol for live imaging, and demonstrate increased lethality associated with viral infection and encephalitis in mutant mice lacking Dicer activity. Our data indicate that miRNAs are important players in the control of MCMV pathogenesis and suggest that miRNA-based endothelial functions and integrity are crucial for CMV encephalitis.
机译:在疱疹病毒中,人类巨细胞病毒(HCMV或HHV-5)在先天或新生儿感染期间代表了主要威胁,可能导致脑炎,并带来严重的神经系统后果。但是,与其他不太普遍的病原体相反,对CMV脑炎的机制和遗传易感性因素知之甚少。信息的缺乏大大降低了预后和/或治疗的可能性。为了方便地监测CMV感染后遗传缺陷对脑扩散的影响,我们使用了一种新近开发的体内小鼠模型,该模型基于新生儿接种的基因工程化表达荧光素酶的MCMV。在这里,我们进一步验证该协议的实时成像,并证明在缺乏Dicer活性的突变小鼠中与病毒感染和脑炎相关的致死率增加。我们的数据表明,miRNA是控制MCMV发病机制的重要参与者,并表明基于miRNA的内皮功能和完整性对​​于CMV脑炎至关重要。

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