Pathogenic difference of respiratory syncytial virus infection in cotton rats of different ages

棉鼠 病毒 呼吸系统 免疫学 免疫 发病机制 生物 下呼吸道感染 医学 病毒学 病毒载量 炎症 粘液 肺病毒科 副粘病毒科 呼吸道 免疫系统 病菌 呼吸道感染 病毒性疾病 内科学 生态学
作者
Xiang Wen,Shi Mo,Shenglin Chen,Guangyuan Yu,Leiqiong Gao,Sisi Chen,Yu Deng,Xiaohong Xie,Na Zang,Ren Luo,Enmei Liu
出处
期刊:Microbial Pathogenesis [Elsevier]
卷期号:137: 103749-103749 被引量:9
标识
DOI:10.1016/j.micpath.2019.103749
摘要

Human respiratory syncytial virus (RSV) is the most common viral pathogen of lower respiratory tract infection worldwide. The virus selectively infects the respiratory epithelium, and causes diseases of variable severity in infants and the elderly. However, the differences in pathogenesis in the age groups remain poorly studied. Age is a major determinant of RSV disease, and the most severe morbidity and mortality occur in the infants and the elderly, because of the immature immunity in infants and declining immunity in old age. The cotton rat is a good model of RSV infection as it is naturally susceptible to RSV. In this study, we established an infant/adult/elderly RSV infection model in 3-week, 8-week and 30-week-old cotton rats and infected them with equal dose of RSV. This model exhibited airway neutrophils infiltration. In the 3-week-old group, higher viral load was observed in the lungs and noses, may due to low IFN-α/Mx2 levels. In contrast, the 8-week-old group had adequate IFN-α/Mx2 but exhibited the most obvious pulmonary inflammation and peribronchiolitis. Interestingly, the most severe pathology and delayed viral clearance in the lungs were observed in the 30-week-old group, may related to the increase of mucus induced by TNF-α and the lower antiviral effect of IFN-α. These results clearly revealed that an age-dependent severity of RSV disease and antiviral defense in the cotton rats, which may provide an effective model for personalized vaccine research and specific treatment strategies for different RSV age groups.
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