Wang Xiuqing, Rosa Artur J M, Oliverira Henrique N, Rosa Guilherme J M, Guo Xueshui, Travnicek Mark, Girshick Theodore
Department of Biology and Microbiology, South Dakota State University, Brookings, SD 57007, USA.
Viral Immunol. 2006 Winter;19(4):768-74. doi: 10.1089/vim.2006.19.768.
To understand the mechanistic basis of local innate and adaptive immunity against infectious bronchitis virus (IBV) at the molecular level, we examined the gene transcription profile of tracheal epithelial layers 3 d after infection of chickens with an attenuated IBV-Massachusetts strain. Results suggested that the transcription levels of 365 genes were either upregulated or downregulated (2-fold and higher) after IBV infection. Among the upregulated 250 genes, 25 were directly immune-related genes. These upregulated immune response genes included TLR2, TLR3, interferon-induced antiviral genes (Mx), and genes responsible for cytotoxic T cell killing such as Fas antigen and granzyme-A. Overall, a diversity of innate immunity and helper T cell type 1 (Th1)-biased adaptive immunity are activated in the host's early defense against IBV invasion, and they are responsible for the rapid clearance of virus from the local infection.
为了在分子水平上理解针对传染性支气管炎病毒(IBV)的局部固有免疫和适应性免疫的机制基础,我们检测了用减毒的IBV-马萨诸塞州毒株感染鸡3天后气管上皮层的基因转录谱。结果表明,IBV感染后365个基因的转录水平上调或下调(2倍及以上)。在250个上调基因中,25个是直接免疫相关基因。这些上调的免疫反应基因包括TLR2、TLR3、干扰素诱导的抗病毒基因(Mx),以及负责细胞毒性T细胞杀伤的基因,如Fas抗原和颗粒酶-A。总体而言,在宿主早期抵御IBV入侵的过程中,多种固有免疫和以辅助性T细胞1型(Th1)为主的适应性免疫被激活,它们负责从局部感染中快速清除病毒。