Department of Biology, University of North Carolina at Greensboro, Greensboro, NC 27402, USA; Department of Entomology & Plant Pathology, North Carolina State University, Raleigh, NC 27695, USA.
Department of Biology, University of North Carolina at Greensboro, Greensboro, NC 27402, USA.
Infect Genet Evol. 2020 Nov;85:104558. doi: 10.1016/j.meegid.2020.104558. Epub 2020 Sep 16.
Trans-generational disease effects include vertical pathogen transmission but also immune priming to enhance offspring immunity. Accordingly, the survival consequences of maternal virus infection can vary and its molecular consequences during early development are poorly understood. The honey bee queen is long-lived and represents the central hub for vertical virus transmission as the sole reproductive individual in her colony. Even though virus symptoms in queens are mild, viral infection may have severe consequences for the offspring. Thus, transcriptome patterns during early developmental are predicted to respond to maternal virus infection. To test this hypothesis, gene expression patterns were compared among pooled honey bee eggs laid by queens that were either infected with Deformed wing virus (DWV), Sacbrood virus (SBV), both viruses (DWV and SBV), or no virus. Whole transcriptome analyses revealed significant expression differences of a few genes, some of which have hitherto no known function. Despite the paucity of single gene effects, functional enrichment analyses revealed numerous biological processes in the embryos to be affected by virus infection. Effects on several regulatory pathways were consistent with maternal responses to virus infection and correlated with responses to DWV and SBV in honey bee larvae and pupae. Overall, effects on egg transcriptome patterns were specific to each virus and the results of dual-infection samples suggested synergistic effects of DWV and SBV. We interpret our results as consequences of maternal infections. Thus, this first study to document and characterize virus-associated changes in the transcriptome of honey bee eggs represents an important contribution to understanding trans-generational virus effects, although more in-depth studies are needed to understand the detailed mechanisms of how viruses affect honey bee embryos.
代际疾病效应包括垂直病原体传播,但也有免疫启动作用,以增强后代的免疫力。因此,母体病毒感染的生存后果可能会有所不同,其在早期发育过程中的分子后果也知之甚少。蜂王寿命长,是垂直病毒传播的中心枢纽,因为她是蜂群中唯一的繁殖个体。尽管蜂王的病毒症状较轻,但病毒感染可能对后代产生严重后果。因此,早期发育过程中的转录组模式预计会对母体病毒感染做出反应。为了验证这一假设,比较了感染了变形翅膀病毒(DWV)、Sacbrood 病毒(SBV)、两种病毒(DWV 和 SBV)或没有病毒的蜂王所产的 pooled honey bee eggs 中的基因表达模式。全转录组分析显示,少数基因的表达差异显著,其中一些基因迄今尚无已知功能。尽管单个基因的影响很少,但功能富集分析显示,病毒感染会影响胚胎中的许多生物学过程。对几个调节途径的影响与母体对病毒感染的反应一致,并与 DWV 和 SBV 在蜜蜂幼虫和蛹中的反应相关。总体而言,病毒对卵转录组模式的影响是特定于每种病毒的,双感染样本的结果表明 DWV 和 SBV 具有协同作用。我们将这些结果解释为母体感染的后果。因此,这项首次记录和描述蜜蜂卵中转录组与病毒相关变化的研究,为理解代际病毒效应做出了重要贡献,尽管需要更深入的研究来了解病毒如何影响蜜蜂胚胎的详细机制。