Wang Jianlin, Cao Zhiwei, Guo Xuejin, Zhang Yi, Wang Dongdong, Xu Shouzheng, Yin Yanbo
a College of Animal Science and Technology, Qingdao Agricultural University , Qingdao , People's Republic of China.
b China Animal Health and Epidemiology Center , Qingdao , People's Republic of China.
Avian Pathol. 2016 Dec;45(6):630-639. doi: 10.1080/03079457.2016.1193665. Epub 2016 Oct 6.
SD/818 and SD/196 are H9N2 influenza virus strains isolated from chickens from the same farm at different times that exhibited similar genetic evolution. However, strain SD/818 exhibited higher pathogenicity in chickens than strain SD/196 and other H9N2 influenza virus epidemic strains from China. The expression of cytokines is an important host defence mechanism following viral infection and their intensity is a major determinant of viral pathogenicity. To elucidate the mechanism underlying the increased pathogenicity of strain SD/818 from the host's perspective, viral replication and cytokine expression were dynamically studied using real-time quantitative reverse transcription PCR in chickens infected with strain SD/818 compared with chickens infected with strain SD/196 in this study. The results showed that the replication of strain SD/818 and the expressions of IL-1β, IL-6, TNF-α, IFN-α and IFN-β induced by strain SD/818 were higher than those induced by strain SD/196 in the chicken host system. Expression of these cytokines in chickens coincided with or followed virus replication. These results suggested that high-level viral replication and pro-inflammatory cytokine expression (but not decreased type I IFN expression) were associated with the higher pathogenicity of strain SD/818 in chickens.
SD/818和SD/196是从同一养殖场不同时间的鸡中分离出的H9N2流感病毒株,它们呈现出相似的基因进化。然而,SD/818毒株在鸡中的致病性高于SD/196毒株以及来自中国的其他H9N2流感病毒流行毒株。细胞因子的表达是病毒感染后重要的宿主防御机制,其强度是病毒致病性的主要决定因素。为了从宿主角度阐明SD/818毒株致病性增强的机制,本研究通过实时定量逆转录PCR动态研究了感染SD/818毒株的鸡与感染SD/196毒株的鸡的病毒复制和细胞因子表达。结果显示,在鸡宿主系统中,SD/818毒株的复制以及由SD/818毒株诱导的IL-1β、IL-6、TNF-α、IFN-α和IFN-β的表达均高于SD/196毒株诱导的水平。这些细胞因子在鸡中的表达与病毒复制同时发生或在病毒复制之后。这些结果表明,高水平的病毒复制和促炎细胞因子表达(而非I型干扰素表达降低)与SD/818毒株在鸡中的较高致病性相关。