Department of Biological Sciences, University of Alberta, Edmonton, AB, Canada.
Li Ka Shing Institute of Virology, University of Alberta, Edmonton, AB, Canada.
Front Cell Infect Microbiol. 2020 May 12;10:209. doi: 10.3389/fcimb.2020.00209. eCollection 2020.
Mallard ducks are a natural host and reservoir of avian Influenza A viruses. While most influenza strains can replicate in mallards, the virus typically does not cause substantial disease in this host. Mallards are often resistant to disease caused by highly pathogenic avian influenza viruses, while the same strains can cause severe infection in humans, chickens, and even other species of ducks, resulting in systemic spread of the virus and even death. The differences in influenza detection and antiviral effectors responsible for limiting damage in the mallards are largely unknown. Domestic mallards have an early and robust innate response to infection that seems to limit replication and clear highly pathogenic strains. The regulation and timing of the response to influenza also seems to circumvent damage done by a prolonged or dysregulated immune response. Rapid initiation of innate immune responses depends on viral recognition by pattern recognition receptors (PRRs) expressed in tissues where the virus replicates. RIG-like receptors (RLRs), Toll-like receptors (TLRs), and Nod-like receptors (NLRs) are all important influenza sensors in mammals during infection. Ducks utilize many of the same PRRs to detect influenza, namely RIG-I, TLR7, and TLR3 and their downstream adaptors. Ducks also express many of the same signal transduction proteins including TBK1, TRIF, and TRAF3. Some antiviral effectors expressed downstream of these signaling pathways inhibit influenza replication in ducks. In this review, we summarize the recent advances in our understanding of influenza recognition and response through duck PRRs and their adaptors. We compare basal tissue expression and regulation of these signaling components in birds, to better understand what contributes to influenza resistance in the duck.
绿头鸭是甲型流感病毒的天然宿主和储存库。虽然大多数流感株可以在绿头鸭中复制,但该病毒通常不会在这种宿主中引起严重疾病。绿头鸭通常对高致病性禽流感病毒引起的疾病有抵抗力,而同一毒株可导致人类、鸡,甚至其他种类的鸭子严重感染,导致病毒在体内传播,甚至死亡。导致绿头鸭对流感检测和抗病毒效应物的差异在很大程度上是未知的。家养绿头鸭对感染有早期和强大的先天反应,这似乎限制了病毒的复制并清除了高致病性毒株。对流感的反应的调节和时机似乎也避免了由延长或失调的免疫反应造成的损害。先天免疫反应的快速启动取决于病毒在病毒复制的组织中被模式识别受体(PRRs)识别。在感染期间,RIG 样受体(RLRs)、Toll 样受体(TLRs)和 Nod 样受体(NLRs)都是哺乳动物中重要的流感传感器。鸭子利用许多相同的 PRRs 来检测流感,即 RIG-I、TLR7 和 TLR3 及其下游衔接子。鸭子还表达许多相同的信号转导蛋白,包括 TBK1、TRIF 和 TRAF3。这些信号通路下游表达的一些抗病毒效应物抑制了鸭子中的流感复制。在这篇综述中,我们总结了最近在我们通过鸭 PRRs 及其衔接子理解流感识别和反应方面的进展。我们比较了这些信号成分在鸟类中的基础组织表达和调节,以更好地了解是什么导致了鸭子对流感的抵抗力。