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环境应激在无症状病毒感染期间导致致命性神经创伤。

Environmental Stress Causes Lethal Neuro-Trauma during Asymptomatic Viral Infections.

作者信息

Chow Jonathan, Márka Zsuzsa, Bartos Imre, Márka Szabolcs, Kagan Jonathan C

机构信息

Harvard Medical School and Division of Gastroenterology, Boston Children's Hospital, Boston, MA, USA.

Department of Physics, Columbia University, New York, NY, USA.

出版信息

Cell Host Microbe. 2017 Jul 12;22(1):48-60.e5. doi: 10.1016/j.chom.2017.06.010.

Abstract

Asymptomatic infections often proceed undetected, yet can still prime the host to be sensitive to secondary environmental stress. While the mechanisms underlying disease caused by asymptomatic infections are unknown, it is believed that productive pathogen replication is required. We report that the environmental stress of carbon dioxide (CO) anesthesia converts an asymptomatic rhabdovirus infection in Drosophila to one that is lethal. This lethality results from a pool of infectious virus in glial cells and is regulated by the antiviral RNAi pathway of the host. CO sensitivity is caused by the fusogenic activity of the viral glycoprotein, which results in fusion of neurons and glia. Expression of the viral glycoprotein, but not a fusion defective mutant, is sufficient to cause CO sensitivity, which can occur even in the absence of productive viral replication. These findings highlight how viral proteins, independent of pathogen replication, may predispose hosts to life-threatening environmental stress.

摘要

无症状感染往往未被察觉,但仍可使宿主对继发性环境应激敏感。虽然无症状感染引发疾病的潜在机制尚不清楚,但据信需要有活性的病原体复制。我们报告,二氧化碳(CO)麻醉的环境应激可将果蝇中的无症状弹状病毒感染转变为致死性感染。这种致死性源于神经胶质细胞中的感染性病毒库,并受宿主抗病毒RNAi途径调控。CO敏感性是由病毒糖蛋白的融合活性引起的,这会导致神经元和神经胶质细胞融合。病毒糖蛋白的表达,而非融合缺陷突变体的表达,足以引起CO敏感性,即使在没有活性病毒复制的情况下也可能发生。这些发现凸显了病毒蛋白如何独立于病原体复制而使宿主易受危及生命的环境应激影响。

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