Institute for Antiviral Research, Department of Animal, Dairy, and Veterinary Sciences, 5600 Old Main Hill, Utah State University, Logan, Utah, 84322-5600, United States of America.
Institute of Biology, University of Campinas, Campinas, SP, Brazil.
Sci Rep. 2019 Dec 20;9(1):19531. doi: 10.1038/s41598-019-55717-3.
Clinical evidence is mounting that Zika virus can contribute to Guillain-Barré syndrome which causes temporary paralysis, yet the mechanism is unknown. We investigated the mechanism of temporary acute flaccid paralysis caused by Zika virus infection in aged interferon αβ-receptor knockout mice used for their susceptibility to infection. Twenty-five to thirty-five percent of mice infected subcutaneously with Zika virus developed motor deficits including acute flaccid paralysis that peaked 8-10 days after viral challenge. These mice recovered within a week. Despite Zika virus infection in the spinal cord, motor neurons were not destroyed. We examined ultrastructures of motor neurons and synapses by transmission electron microscopy. The percent coverage of motor neurons by boutons was reduced by 20%; more specifically, flattened-vesicle boutons were reduced by 46%, and were normalized in recovering mice. Using electromyographic procedures employed in people to help diagnose Guillain-Barré syndrome, we determined that nerve conduction velocities between the sciatic notch and the gastrocnemius muscle were unchanged in paralyzed mice. However, F-wave latencies were increased in paralyzed mice, which suggests that neuropathy may exist between the sciatic notch to the nerve rootlets. Reversible synaptic retraction may be a previously unrecognized cofactor along with peripheral neuropathy for the development of Guillain-Barré syndrome during Zika virus outbreaks.
越来越多的临床证据表明寨卡病毒可导致吉兰-巴雷综合征,进而引发暂时性瘫痪,但具体机制尚不清楚。我们研究了用于感染研究的对寨卡病毒易感的干扰素 αβ-受体敲除老龄小鼠中寨卡病毒感染导致的暂时性急性弛缓性麻痹的机制。25%-35%经皮下感染寨卡病毒的小鼠出现运动功能障碍,包括急性弛缓性麻痹,该症状在病毒攻击后 8-10 天达到高峰。这些小鼠在一周内恢复。尽管脊髓中存在寨卡病毒感染,但运动神经元并未被破坏。我们通过透射电子显微镜检查运动神经元和突触的超微结构。被神经末梢覆盖的运动神经元比例降低了 20%;更具体地说,扁平囊泡末梢降低了 46%,而在恢复的小鼠中则恢复正常。我们使用了在人类中用于帮助诊断吉兰-巴雷综合征的肌电图程序,确定瘫痪小鼠坐骨切迹和腓肠肌之间的神经传导速度没有变化。然而,瘫痪小鼠的 F 波潜伏期增加,这表明在坐骨切迹到神经根之间可能存在神经病。可逆性突触回缩可能是寨卡病毒爆发期间吉兰-巴雷综合征发展的一个以前未被认识到的共因子,与周围神经病一起。