Zhan Luting, Zhao Min, Yi Han, Zhang Wei, Cao Jianli, Sun Yongpeng, Zhang Lujing, Si Junyu, Xia Ningshao, Zheng Zizheng
Bing Du Xue Bao. 2016 Jul;32(4):411-6.
Respiratory syncytial virus(RSV)is a leading cause of lower respiratory tract disease. The major high risk population for RSV infection are<6month infants and elders with age older than 65 years. At present, BALB/c mice were wildly used as animal model for RSV infection, however there has no report about the comparison of different week-ages BALB/c mice after RSV infection. A different week-ages BALB/c mice model was described in this study to compare their susceptibility after RSV infection. Young(10weeks),middle aged(30weeks)and aged(60weeks)mice were intranasally infected with 106 or 107plaque-forming units (PFU) RSV, then clinical symptom, weight, RSV titer in nose/lung, histology and immunohistochemistry was examined. And age-related susceptibility was analyzed. A high-titer virus(107PFU)infection showed significant weight loss at 6-11 day post infection while 106 PFU didn’t lead to obvious weight change. In 10(7) PFU infected group, replication of virus in nose and lung was detected, the virus in lung located around pulmonary alveoli, and the hematoxylin eosin stain showed significant infiltration of inflammatory cells and pathological tissue damage. Mice trended to be more susceptible to RSV infection as the growth of age. Older mice experience more weight loss. Lung histology of older mice showed more serious bronchiolitis and increased number of inflammatory cells in alveolar spaced, and 60week-old mice tended to be the most significant. In this study, we have successfully established a different week-ages BALB/c mice model, which will serve as the basis for investigating antibody or vaccine and further infection mechanism research of RSV.
呼吸道合胞病毒(RSV)是下呼吸道疾病的主要病因。RSV感染的主要高危人群是6个月以下的婴儿和65岁以上的老年人。目前,BALB/c小鼠被广泛用作RSV感染的动物模型,然而,关于RSV感染后不同周龄BALB/c小鼠的比较尚无报道。本研究描述了一种不同周龄的BALB/c小鼠模型,以比较它们在RSV感染后的易感性。将年轻(10周)、中年(30周)和老年(60周)小鼠经鼻感染10⁶或10⁷空斑形成单位(PFU)的RSV,然后检查其临床症状、体重、鼻/肺中的RSV滴度、组织学和免疫组织化学。并分析了与年龄相关的易感性。高滴度病毒(10⁷PFU)感染在感染后6-11天显示出显著的体重减轻,而10⁶PFU未导致明显的体重变化。在10⁷PFU感染组中,检测到病毒在鼻和肺中的复制,肺中的病毒位于肺泡周围,苏木精伊红染色显示炎性细胞显著浸润和病理组织损伤。随着年龄的增长,小鼠对RSV感染的易感性增加。老年小鼠体重减轻更多。老年小鼠的肺组织学显示细支气管炎更严重,肺泡间隔中的炎性细胞数量增加,60周龄的小鼠往往最为明显。在本研究中,我们成功建立了不同周龄的BALB/c小鼠模型,这将为研究RSV的抗体或疫苗以及进一步的感染机制研究奠定基础。