Chen Shilong, Wang Long, Chen Jieying, Zhang Lanlan, Wang Song, Goraya Mohsan U, Chi Xiaojuan, Na Yang, Shao Wenhan, Yang Zhou, Zeng Xiancheng, Chen Shaoying, Chen Ji-Long
Key Laboratory of Fujian-Taiwan Animal Pathogen Biology, College of Animal Sciences, Fujian Agriculture and Forestry UniversityFuzhou, China.
Key Laboratory of Animal Virology, Institute of Animal Husbandry and Veterinary Medicine, Fujian Academy of Agriculture SciencesFuzhou, China.
Front Microbiol. 2017 Apr 20;8:672. doi: 10.3389/fmicb.2017.00672. eCollection 2017.
Avian Tembusu virus (ATMUV) is a highly pathogenic flavivirus that causes significant economic losses to the Chinese poultry industry. Our previous experiments demonstrated that ATMUV infection effectively triggered host innate immune response through MDA5 and TLR3-dependent signaling pathways. However, little information is available on the role of interferon-stimulated genes (ISGs) in defending against ATMUV infection. In this study, we found that ATMUV infection induced robust expression of type I and type III interferon (IFNs) in duck tissues. Furthermore, we observed that expression of interferon-inducible transmembrane proteins (IFITMs) was significantly upregulated in DEF and DF-1 cells after infection with ATMUV. Similar results were obtained from studies using ATMUV-infected ducklings. Importantly, we showed that knockdown of endogenous IFITM1 or IFITM3 by specific shRNA markedly enhanced ATMUV replication in DF-1 cells. However, disruption of IFITM2 expression had no obvious effect on the ATMUV replication. In addition, overexpression of chicken or duck IFITM1 and IFITM3 in DF-1 cells impaired the replication of ATMUV. Taken together, these results reveal that induced expression of avian IFITM1 and IFITM3 in response to ATMUV infection can effectively restrict the virus replication, and suggest that increasing IFITM proteins in host may be a useful strategy for control of ATMUV infection.
禽坦布苏病毒(ATMUV)是一种高致病性黄病毒,给中国家禽业造成了重大经济损失。我们之前的实验表明,ATMUV感染通过MDA5和TLR3依赖的信号通路有效触发宿主固有免疫反应。然而,关于干扰素刺激基因(ISGs)在抵御ATMUV感染中的作用,目前所知甚少。在本研究中,我们发现ATMUV感染可诱导鸭组织中I型和III型干扰素(IFNs)的强烈表达。此外,我们观察到,用ATMUV感染DEF和DF-1细胞后,干扰素诱导跨膜蛋白(IFITMs)的表达显著上调。使用感染ATMUV的雏鸭进行的研究也得到了类似结果。重要的是,我们发现通过特异性短发夹RNA敲低内源性IFITM1或IFITM3可显著增强DF-1细胞中ATMUV的复制。然而,破坏IFITM2的表达对ATMUV的复制没有明显影响。此外,在DF-1细胞中过表达鸡或鸭的IFITM1和IFITM3会损害ATMUV的复制。综上所述,这些结果表明,禽IFITM1和IFITM3在响应ATMUV感染时的诱导表达可有效限制病毒复制,并表明增加宿主中的IFITM蛋白可能是控制ATMUV感染的一种有效策略。