The Dynamics of Deformed Wing Virus Concentration and Host Defensive Gene Expression after Varroa Mite Parasitism in Honey Bees, Apis mellifera

文献类型： 外文期刊

第一作者： Zhao, Yazhou

作者： Zhao, Yazhou;Heerman, Matthew;Evans, Jay D.;Li, Jianghong;Li, Zhiguo;Cook, Steven C.;Rodriguez-Garcia, Cristina;Banmeke, Olubukola;Hamilton, Michele;Chen, Yanping;Zhao, Yazhou;Peng, Wenjun;Rose, Robyn;DeGrandi-Hoffman, Gloria;Simone-Finstrom, Michael;Li, Jianghong;Li, Zhiguo;Su, Songkun;Rodriguez-Garcia, Cristina

作者机构：

关键词： honeybee; Varroa-DWV interaction; DWV titers; immune gene expression; anti-pathogen mechanisms

期刊名称：INSECTS （ 影响因子：2.769； 五年影响因子：3.046 ）

ISSN： 2075-4450

年卷期： 2019 年 10 卷 1 期

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收录情况： SCI

摘要： The synergistic interactions between the ectoparasitic mite Varroa destructor and Deformed wing virus (DWV) lead to the reduction in lifespan of the European honey bee Apis mellifera and often have been implicated in colony losses worldwide. However, to date, the underlying processes and mechanisms that form the multipartite interaction between the bee, mite, and virus have not been fully explained. To gain a better understanding of honey bees' defense response to Varroa mite infestation and DWV infection, the DWV titers and transcription profiles of genes originating from RNAi, immunity, wound response, and homeostatic signaling pathways were monitored over a period of eight days. With respect to DWV, we observed low viral titers at early timepoints that coincided with high levels of Toll pathway transcription factor Dorsal, and its downstream immune effector molecules Hymenoptaecin, Apidaecin, Abaecin, and Defensin 1. However, we observed a striking increase in viral titers beginning after two days that coincided with a decrease in Dorsal levels and its corresponding immune effector molecules, and the small ubiquitin-like modifier (SUMO) ligase repressor of Dorsal, PIAS3. We observed a similar expression pattern for genes expressing transcripts for the RNA interference (Dicer/Argonaute), wound/homeostatic (Janus Kinase), and tissue growth (Map kinase/Wnt) pathways. Our results demonstrate that on a whole, honey bees are able to mount an immediate, albeit, temporally limited, immune and homeostatic response to Varroa and DWV infections, after which downregulation of these pathways leaves the bee vulnerable to expansive viral replication. The critical insights into the defense response upon Varroa and DWV challenges generated in this study may serve as a solid base for future research on the development of effective and efficient disease management strategies in honey bees.

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