Zheng Hui-Wen, Sun Ming, Guo Lei, Wang Jing-Jing, Song Jie, Li Jia-Qi, Li Hong-Zhe, Ning Ruo-Tong, Yang Ze-Ning, Fan Hai-Tao, He Zhan-Long, Liu Long-Ding
Institute of Medical Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Kunming 650118, China.
Viruses. 2017 May 10;9(5):104. doi: 10.3390/v9050104.
Data from EV-D68-infected patients demonstrate that pathological changes in the lower respiratory tract are principally characterized by severe respiratory illness in children and acute flaccid myelitis. However, lack of a suitable animal model for EV-D68 infection has limited the study on the pathogenesis of this critical pathogen, and the development of a vaccine. Ferrets have been widely used to evaluate respiratory virus infections. In the current study, we used EV-D68-infected ferrets as a potential animal to identify impersonal indices, involving clinical features and histopathological changes in the upper and lower respiratory tract (URT and LRT). The research results demonstrate that the EV-D68 virus leads to minimal clinical symptoms in ferrets. According to the viral load detection in the feces, nasal, and respiratory tracts, the infection and shedding of EV-D68 in the ferret model was confirmed, and these results were supported by the EV-D68 VP1 immunofluorescence confocal imaging with α2,6-linked sialic acid (SA) in lung tissues. Furthermore, we detected the inflammatory cytokine/chemokine expression level, which implied high expression levels of interleukin (IL)-1a, IL-8, IL-5, IL-12, IL-13, and IL-17a in the lungs. These data indicate that systemic observation of responses following infection with EV-D68 in ferrets could be used as a model for EV-D68 infection and pathogenesis.
来自肠道病毒D68(EV-D68)感染患者的数据表明,下呼吸道的病理变化主要表现为儿童严重呼吸道疾病和急性弛缓性脊髓炎。然而,缺乏合适的EV-D68感染动物模型限制了对这种关键病原体发病机制的研究以及疫苗的研发。雪貂已被广泛用于评估呼吸道病毒感染。在本研究中,我们使用感染EV-D68的雪貂作为潜在动物来确定客观指标,包括上、下呼吸道(URT和LRT)的临床特征和组织病理学变化。研究结果表明,EV-D68病毒在雪貂中引起的临床症状轻微。根据粪便、鼻腔和呼吸道中的病毒载量检测,证实了EV-D68在雪貂模型中的感染和排出,并且肺组织中与α2,6-连接唾液酸(SA)结合的EV-D68 VP1免疫荧光共聚焦成像支持了这些结果。此外,我们检测了炎性细胞因子/趋化因子的表达水平,结果表明肺中白细胞介素(IL)-1α、IL-8、IL-5、IL-12、IL-13和IL-17α表达水平较高。这些数据表明,对感染EV-D68的雪貂感染后反应进行系统观察可作为EV-D68感染和发病机制的模型。