Institute of Preventive Veterinary Medicine, Sichuan Agricultural University, Wenjiang, China.
Avian Disease Research Center, College of Veterinary Medicine of Sichuan Agricultural University, Wenjiang, China.
Front Cell Infect Microbiol. 2020 Apr 15;10:155. doi: 10.3389/fcimb.2020.00155. eCollection 2020.
Duck tembusu virus (DTMUV) is newly emerged in poultry and causes great losses to the breeding industry in China and neighboring countries. Effective antiviral strategies are still being studied. Autophagy is a cellular degradative pathway, and our lab's previous data show that autophagy promotes DTMUV replication . To study the role of autophagy further , we utilized ducks as the animal model to investigate the autophagy responses in DTMUV-targeted tissues. And also, we utilized autophagy regulators, including Rapamycin (Rapa) as the autophagy enhancer, 3-Methyladenine (3-MA) and Chloroquine (CQ) as the autophagy inhibitors, to adjust the host autophagic levels and then study the effects of autophagy on tissue damages and virus replication. As a result, we first found DTMUV infection trigged autophagy and autophagy regulator treatments regulated autophagy levels successfully in duck spleens and brains. Next, we found that autophagy inhibitors inhibited DTMUV replication and alleviated DTMUV-induced pathological symptoms, whereas the autophagy inducer treatment led to the opposite effects. And we also found that autophagic regulation was correlated with the expression of innate immune genes, including pattern recognition receptors, type I interferons, and cytokines, and caused different effects in different tissues. In summary, we demonstrated that autophagy facilitated DTMUV replication, aggravated the developments of pathological symptoms and possibly counteracts the host's innate immunity response .
鸭坦布苏病毒(DTMUV)是一种新兴的禽类病毒,给中国及周边国家的养殖业带来了巨大的损失。目前仍在研究有效的抗病毒策略。自噬是一种细胞降解途径,我们实验室之前的数据表明自噬可以促进 DTMUV 的复制。为了进一步研究自噬的作用,我们利用鸭子作为动物模型,研究 DTMUV 靶向组织中的自噬反应。此外,我们还利用自噬调节剂,包括雷帕霉素(Rapa)作为自噬增强剂、3-甲基腺嘌呤(3-MA)和氯喹(CQ)作为自噬抑制剂,调节宿主的自噬水平,然后研究自噬对组织损伤和病毒复制的影响。结果,我们首先发现 DTMUV 感染触发了自噬,并且自噬调节剂处理成功地调节了鸭脾脏和大脑中的自噬水平。接下来,我们发现自噬抑制剂抑制了 DTMUV 的复制并减轻了 DTMUV 诱导的病理症状,而自噬诱导剂处理则产生了相反的效果。我们还发现,自噬调节与先天免疫基因的表达有关,包括模式识别受体、I 型干扰素和细胞因子,并在不同组织中产生不同的效果。总之,我们证明了自噬促进了 DTMUV 的复制,加重了病理症状的发展,并可能抵消了宿主的先天免疫反应。