Vijayakumar Periyasamy, Mishra Anamika, Ranaware Pradip B, Kolte Atul P, Kulkarni Diwakar D, Burt David W, Raut Ashwin Ashok
High Security Animal Disease Laboratory, Indian Veterinary Research Institute, Anand Nagar, Bhopal 462021, Madhya Pradesh, India.
High Security Animal Disease Laboratory, Indian Veterinary Research Institute, Anand Nagar, Bhopal 462021, Madhya Pradesh, India.
Gene. 2015 Mar 15;559(1):77-85. doi: 10.1016/j.gene.2015.01.016. Epub 2015 Jan 12.
The highly pathogenic avian influenza (HPAI) H5N1 virus, currently circulating in Asia, causes severe disease in domestic poultry as well as wild birds like crow. However, the molecular pathogenesis of HPAIV infection in crows and other wild birds is not well known. Thus, as a step to explore it, a comprehensive global gene expression analysis was performed on crow lungs, infected with HPAI H5N1 crow isolate (A/Crow/India/11TI11/2011) using high throughput next generation sequencing (NGS) (GS FLX Titanium XLR70). The reference genome of crow is not available, so RNA seq analysis was performed on the basis of a de novo assembled transcriptome. The RNA seq result shows, 4052 genes were expressed uniquely in noninfected, 6277 genes were expressed uniquely in HPAIV infected sample and of the 6814 genes expressed in both samples, 2279 genes were significantly differentially expressed. Our transcriptome profile data allows for the ability to understand the molecular mechanism behind the recent lethal HPAIV outbreak in crows which was, until recently, thought to cause lethal infections only in gallinaceous birds such as chickens, but not in wild birds. The pattern of differentially expressed genes suggest that this isolate of H5N1 virus evades the host innate immune response by attenuating interferon (IFN)-inducible signalling possibly by down regulating the signalling from type I IFN (IFNAR1 and IFNAR2) and type II IFN receptors, upregulation of the signalling inhibitors suppressor of cytokine signalling 1 (SOCS1) and SOCS3 and altering the expression of toll-like receptors (TLRs). This may be the reason for disease and mortality in crows.
目前在亚洲传播的高致病性禽流感(HPAI)H5N1病毒,可在家禽以及乌鸦等野生鸟类中引发严重疾病。然而,HPAIV在乌鸦和其他野生鸟类中感染的分子发病机制尚不清楚。因此,作为探索该机制的第一步,我们使用高通量新一代测序(NGS)(GS FLX Titanium XLR70)技术,对感染HPAI H5N1乌鸦分离株(A/乌鸦/印度/11TI11/2011)的乌鸦肺部进行了全面的全球基因表达分析。由于乌鸦的参考基因组不可用,因此基于从头组装的转录组进行了RNA测序分析。RNA测序结果显示,4052个基因在未感染样本中独特表达,6277个基因在HPAIV感染样本中独特表达,在两个样本中均表达的6814个基因中,有2279个基因存在显著差异表达。我们的转录组图谱数据有助于了解最近乌鸦中致命HPAIV爆发背后的分子机制,直到最近,人们一直认为该病毒仅在鸡等家禽类鸟类中引发致命感染,而不会在野生鸟类中引发感染。差异表达基因的模式表明,这种H5N1病毒分离株可能通过下调I型干扰素(IFN)(IFNAR1和IFNAR2)和II型干扰素受体的信号传导、上调细胞因子信号传导抑制因子1(SOCS1)和SOCS3等信号传导抑制剂以及改变Toll样受体(TLR)的表达,来减弱干扰素(IFN)诱导的信号传导,从而逃避宿主的先天免疫反应。这可能是乌鸦发病和死亡的原因。