Norton Amanda M, Buchmann Gabriele, Ashe Alyson, Watson Owen T, Beekman Madeleine, Remnant Emily J
School of Life and Environmental Sciences, The University of Sydney, Sydney, New South Wales, Australia.
Insect Mol Biol. 2025 Feb;34(1):33-51. doi: 10.1111/imb.12948. Epub 2024 Jul 27.
Iflavirus aladeformis (Picornavirales: Iflaviridae), commonly known as deformed wing virus(DWV), in association with Varroa destructor Anderson and Trueman (Mesostigmata: Varroidae), is a leading factor associated with honey bee (Apis mellifera L. [Hymenoptera: Apidae]) deaths. The virus and mite have a near global distribution, making it difficult to separate the effect of one from the other. The prevalence of two main DWV genotypes (DWV-A and DWV-B) has changed over time, leading to the possibility that the two strains elicit a different immune response by the host. Here, we use a honey bee population naïve to both the mite and the virus to investigate if honey bees show a different immunological response to DWV genotypes. We examined the expression of 19 immune genes by reverse transcription quantitative PCR (RT-qPCR) and analysed small RNA after experimental injection with DWV-A and DWV-B. We found no evidence that DWV-A and DWV-B elicit different immune responses in honey bees. RNA interference genes were up-regulated during DWV infection, and small interfering RNA (siRNA) responses were proportional to viral loads yet did not inhibit DWV accumulation. The siRNA response towards DWV was weaker than the response to another honey bee pathogen, Triatovirus nigereginacellulae (Picornavirales: Dicistroviridae; black queen cell virus), suggesting that DWV is comparatively better at evading host antiviral defences. There was no evidence for the production of virus-derived Piwi-interacting RNAs (piRNAs) in response to DWV. In contrast to previous studies, and in the absence of V. destructor, we found no evidence that DWV has an immunosuppressive effect. Overall, our results advance our understanding of the immunological effect that DWV in isolation elicits in honey bees.
变形翼病毒(Iflavirus aladeformis,属于小RNA病毒目:变形翼病毒科),通常被称为变形翼病毒(DWV),与狄斯瓦螨(Varroa destructor Anderson and Trueman,属于中气门目:瓦螨科)共同作用,是导致蜜蜂(西方蜜蜂Apis mellifera L. [膜翅目:蜜蜂科])死亡的主要因素。该病毒和螨虫几乎遍布全球,这使得很难区分它们各自的影响。两种主要的DWV基因型(DWV-A和DWV-B)的流行率随时间发生了变化,这导致两种毒株可能引发宿主不同免疫反应的可能性。在这里,我们使用对螨虫和病毒均无接触史的蜜蜂群体来研究蜜蜂对DWV基因型是否表现出不同的免疫反应。我们通过逆转录定量PCR(RT-qPCR)检测了19个免疫基因的表达,并在分别注射DWV-A和DWV-B后分析了小RNA。我们没有发现证据表明DWV-A和DWV-B在蜜蜂中引发不同的免疫反应。RNA干扰基因在DWV感染期间上调,小干扰RNA(siRNA)反应与病毒载量成正比,但并未抑制DWV的积累。对DWV的siRNA反应比对另一种蜜蜂病原体——黑蜂王台病毒(Triatovirus nigereginacellulae,属于小RNA病毒目:双顺反子病毒科)的反应要弱,这表明DWV在逃避宿主抗病毒防御方面相对更胜一筹。没有证据表明对DWV感染会产生病毒衍生的Piwi相互作用RNA(piRNA)。与之前的研究不同,在没有狄斯瓦螨的情况下,我们没有发现证据表明DWV具有免疫抑制作用。总体而言,我们的研究结果增进了我们对孤立状态下DWV对蜜蜂免疫影响的理解。