Hu Zenglei, Hu Jiao, Hu Shunlin, Song Qingqing, Ding Pingyun, Zhu Jie, Liu Xiaowen, Wang Xiaoquan, Liu Xiufan
Animal Infectious Disease Laboratory, School of Veterinary Medicine, Yangzhou University, 48 East Wenhui Road, Yangzhou, 225009, Jiangsu, China.
Arch Virol. 2015 Mar;160(3):639-48. doi: 10.1007/s00705-014-2301-2. Epub 2014 Dec 12.
Some strains of Newcastle disease virus (NDV) genotype VIId cause more-severe tissue damage in lymphoid organs compared to other virulent strains. In this study, we aim to define the mechanism of this distinct pathological manifestation of genotype VII viruses. Pathology, virus replication, and the innate immune response in lymphoid tissues of chickens infected with two genotype VIId NDV strains (JS5/05 and JS3/05), genotype IX NDV F48E8 and genotype IV NDV Herts/33, were compared. Histopathologic examination showed that JS5/05 and JS3/05 produced more-severe lesions in the spleen and thymus, but these four virulent strains caused comparable mild lesions in the bursa. In addition, JS3/05 and JS5/05 replicated at significantly higher levels in the lymphatic organs than F48E8 and Herts/33. A microarray assay performed on the spleens of chickens infected with JS5/05 or Herts/33 revealed that JS5/05 elicited a more potent inflammatory response by increasing the number and expression levels of activated genes. Moreover, cytokine gene expression profiling showed that JS5/05 and JS3/05 induced a stronger cytokine response in lymphoid tissues compared to F48E8 and Herts/33. Taken together, our results indicate that the severe pathology in immune organs caused by genotype VIId NDV strains is associated with high levels of virus replication and an intense inflammatory response.
与其他强毒株相比,新城疫病毒(NDV)VII d基因型的某些毒株在淋巴器官中会造成更严重的组织损伤。在本研究中,我们旨在确定VII d基因型病毒这种独特病理表现的机制。我们比较了感染两种VII d基因型NDV毒株(JS5/05和JS3/05)、IX基因型NDV F48E8和IV基因型NDV Herts/33的鸡的淋巴组织中的病理学、病毒复制及天然免疫反应。组织病理学检查显示,JS5/05和JS3/05在脾脏和胸腺中产生了更严重的病变,但这四种强毒株在法氏囊中引起的轻微病变程度相当。此外,JS3/05和JS5/05在淋巴器官中的复制水平显著高于F48E8和Herts/33。对感染JS5/05或Herts/33的鸡的脾脏进行的微阵列分析显示,JS5/05通过增加活化基因的数量和表达水平引发了更强的炎症反应。此外,细胞因子基因表达谱分析表明,与F48E8和Herts/33相比,JS5/05和JS3/05在淋巴组织中诱导了更强的细胞因子反应。综上所述,我们的结果表明,VII d基因型NDV毒株在免疫器官中引起的严重病理变化与高水平的病毒复制和强烈的炎症反应有关。