Institute of Laboratory Animal Sciences, Chinese Academy of Medical Sciences (CAMS) & Comparative Medicine Center, Peking Union Medical College (PUMC); Key Laboratory of Human Diseases Comparative Medicine, Ministry of Health; Beijing Key Laboratory for Animal Models of Emerging and Reemerging Infectious Diseases, Beijing 100021, China.
Viruses. 2017 Nov 20;9(11):351. doi: 10.3390/v9110351.
Enterovirus 71 (EV71) is a common etiological agent of hand, foot, and mouth disease and fatal neurological diseases in children. The neuropathogenicity of severe EV71 infection has been documented, but studies comparing mouse models of severe and mild EV71 infection are lacking. The aim of the study was to investigate the neurovirulence of EV71 strains and the differences in serum cytokine and chemokine levels in mouse models of severe and mild EV71 infection. Nine EV71 isolates belonging to the C4 subgenogroup (proposed as genotype D) displayed infectivity in human neuroblastoma SK-N-SH cells; moreover, ultrastructural observation confirmed viral particle replication. The survival rate of the severe model was 71.43% (5/7), and 60% (3/5) of the surviving severe model mice displayed sequelae of paralysis, whereas the only symptom in mild model mice was ruffled fur. Dynamic detection of serum cytokine and chemokine levels demonstrated that interleukin (IL)-5, IL-13, IL-6, monocyte chemotactic protein 1 (MCP-1), and chemokine (C-C motif) ligand 5 (also called Regulated upon Activation, Normal T-cell Expressed, and Secreted (CCL5/RANTES) were significantly up-regulated at the early period of infection, indicating that these factors might herald a severe outcome. Our findings suggest that elevated cytokines and chemokines may have potential value as prognostic markers in mouse models.
肠道病毒 71 型(EV71)是引起手足口病和儿童致命性神经系统疾病的常见病原体。严重 EV71 感染的神经致病性已得到证实,但缺乏严重和轻度 EV71 感染小鼠模型的比较研究。本研究旨在探讨 EV71 毒株的神经毒力以及严重和轻度 EV71 感染小鼠模型血清细胞因子和趋化因子水平的差异。属于 C4 亚组(拟议为基因型 D)的 9 株 EV71 分离株在人神经母细胞瘤 SK-N-SH 细胞中具有感染力;此外,超微结构观察证实了病毒颗粒的复制。严重模型的存活率为 71.43%(5/7),存活的严重模型小鼠中有 60%(3/5)出现瘫痪后遗症,而轻度模型小鼠仅出现毛发蓬乱的症状。血清细胞因子和趋化因子水平的动态检测表明,白细胞介素(IL)-5、IL-13、IL-6、单核细胞趋化蛋白 1(MCP-1)和趋化因子(C-C 基序)配体 5(也称为活化正常 T 细胞表达和分泌(RANTES))在感染早期显著上调,表明这些因素可能预示着严重的结果。我们的研究结果表明,升高的细胞因子和趋化因子可能作为小鼠模型中的预后标志物具有潜在价值。