Université de Strasbourg, CNRS, Insect Models of Innate Immunity (M3I; UPR9022), 67084 Strasbourg, France; Sino-French Hoffmann Institute, School of Basic Medical Science, Guangzhou Medical University, Guangzhou 511436, China.
Université de Strasbourg, CNRS, Insect Models of Innate Immunity (M3I; UPR9022), 67084 Strasbourg, France.
Immunity. 2018 Aug 21;49(2):225-234.e4. doi: 10.1016/j.immuni.2018.07.013. Epub 2018 Aug 14.
Antiviral immunity in Drosophila involves RNA interference and poorly characterized inducible responses. Here, we showed that two components of the IMD pathway, the kinase dIKKβ and the transcription factor Relish, were required to control infection by two picorna-like viruses. We identified a set of genes induced by viral infection and regulated by dIKKβ and Relish, which included an ortholog of STING. We showed that dSTING participated in the control of infection by picorna-like viruses, acting upstream of dIKKβ to regulate expression of Nazo, an antiviral factor. Our data reveal an antiviral function for STING in an animal model devoid of interferons and suggest an evolutionarily ancient role for this molecule in antiviral immunity.
果蝇中的抗病毒免疫涉及 RNA 干扰和特征不明确的诱导反应。在这里,我们表明 IMD 途径的两个组成部分,激酶 dIKKβ 和转录因子 Relish,是控制两种类似微小 RNA 病毒感染所必需的。我们鉴定了一组受病毒感染诱导并受 dIKKβ 和 Relish 调控的基因,其中包括 STING 的一个同源物。我们表明 dSTING 参与了类似微小 RNA 病毒感染的控制,在 dIKKβ 的上游作用以调节抗病毒因子 Nazo 的表达。我们的数据揭示了 STING 在缺乏干扰素的动物模型中的抗病毒功能,并表明该分子在抗病毒免疫中具有古老的进化作用。