Miao Ji, Bao Yanqing, Ye Jianqiang, Shao Hongxia, Qian Kun, Qin Aijian
Ministry of Education Key Laboratory for Avian Preventive Medicine, Yangzhou University, Yangzhou, Jiangsu Province, China; Key Laboratory of Jiangsu Preventive Veterinary Medicine, Yangzhou University, Yangzhou, Jiangsu Province, China.
Ministry of Education Key Laboratory for Avian Preventive Medicine, Yangzhou University, Yangzhou, Jiangsu Province, China; Key Laboratory of Jiangsu Preventive Veterinary Medicine, Yangzhou University, Yangzhou, Jiangsu Province, China; Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou University, Yangzhou, Jiangsu Province, China.
PLoS One. 2015 May 14;10(5):e0126992. doi: 10.1371/journal.pone.0126992. eCollection 2015.
Reticuloendotheliosis virus (REV), a member of the Gammaretrovirus genus in the Retroviridae family, causes an immunosuppressive, oncogenic and runting-stunting syndrome in multiple avian hosts. To better understand the host interactions at the transcriptional level, microarray data analysis was performed in chicken embryo fibroblast cells at 1, 3, 5, and 7 days after infection with REV. This study identified 1,785 differentially expressed genes that were classified into several functional groups including signal transduction, immune response, biological adhesion and endocytosis. Significant differences were mainly observed in the expression of genes involved in the immune response, especially during the later post-infection time points. These results revealed that differentially expressed genes IL6, STAT1, MyD88, TLRs, NF-κB, IRF-7, and ISGs play important roles in the pathogenicity of REV infection. Our study is the first to use microarray analysis to investigate REV, and these findings provide insights into the underlying mechanisms of the host antiviral response and the molecular basis of viral pathogenesis.
网状内皮组织增生症病毒(REV)是逆转录病毒科γ逆转录病毒属的成员,可在多种禽类宿主中引起免疫抑制、致癌和生长迟缓综合征。为了在转录水平上更好地了解宿主相互作用,在感染REV后的第1、3、5和7天,对鸡胚成纤维细胞进行了微阵列数据分析。本研究鉴定出1785个差异表达基因,这些基因被分为几个功能组,包括信号转导、免疫反应、生物粘附和内吞作用。主要在参与免疫反应的基因表达中观察到显著差异,尤其是在感染后的后期时间点。这些结果表明,差异表达基因IL6、STAT1、MyD88、TLRs、NF-κB、IRF-7和ISGs在REV感染的致病性中起重要作用。我们的研究是首次使用微阵列分析来研究REV,这些发现为宿主抗病毒反应的潜在机制和病毒发病机制的分子基础提供了见解。