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Tick-Borne Viruses and Biological Processes at the Tick-Host-Virus Interface

机译:Tick-Borne病毒和Tick-Host-Virus界面上的生物过程

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摘要

Ticks are efficient vectors of arboviruses, although less than 10% of tick species are known to be virus vectors. Most tick-borne viruses (TBV) are RNA viruses some of which cause serious diseases in humans and animals world-wide. Several TBV impacting human or domesticated animal health have been found to emerge or re-emerge recently. In order to survive in nature, TBV must infect and replicate in both vertebrate and tick cells, representing very different physiological environments. Information on molecular mechanisms that allow TBV to switch between infecting and replicating in tick and vertebrate cells is scarce. In general, ticks succeed in completing their blood meal thanks to a plethora of biologically active molecules in their saliva that counteract and modulate different arms of the host defense responses (haemostasis, inflammation, innate and acquired immunity, and wound healing). The transmission of TBV occurs primarily during tick feeding and is a complex process, known to be promoted by tick saliva constituents. However, the underlying molecular mechanisms of TBV transmission are poorly understood. Immunomodulatory properties of tick saliva helping overcome the first line of defense to injury and early interactions at the tick-host skin interface appear to be essential in successful TBV transmission and infection of susceptible vertebrate hosts. The local host skin site of tick attachment, modulated by tick saliva, is an important focus of virus replication. Immunomodulation of the tick attachment site also promotes co-feeding transmission of viruses from infected to non-infected ticks in the absence of host viraemia (non-viraemic transmission). Future research should be aimed at identification of the key tick salivary molecules promoting virus transmission, and a molecular description of tick-host-virus interactions and of tick-mediated skin immunomodulation. Such insights will enable the rationale design of anti-tick vaccines that protect against disease caused by tick-borne viruses.
机译:cks虫是虫媒病毒的有效载体,尽管已知不到10%的tick虫是病毒载体。大多数壁虱传播的病毒(TBV)是RNA病毒,其中一些会导致全世界人类和动物的严重疾病。最近发现了几种影响人类或家养动物健康的TBV出现或重新出现。为了在自然中生存,TBV必须在脊椎动物和壁虱细胞中感染并复制,这代表了截然不同的生理环境。 TBV在V和脊椎动物细胞中的感染和复制之间转换的分子机制的信息很少。通常,由于唾液中大量的生物活性分子可以抵消并调节宿主防御反应的不同分支(止血,炎症,先天和后天免疫力以及伤口愈合),因此s虫可以成功地完成其血液餐。 TBV的传播主要发生在tick喂养期间,并且是一个复杂的过程,已知由tick唾液成分促进。但是,对TBV传播的潜在分子机制了解甚少。壁虱唾液的免疫调节特性有助于克服伤害的第一道防线,并且壁虱-宿主皮肤界面的早期相互作用似乎对于成功的TBV传播和易感脊椎动物的感染至关重要。受壁虱唾液调节的壁虱附着的本地宿主皮肤部位是病毒复制的重要焦点。在没有宿主病毒血症的情况下,tick附着部位的免疫调节还促进病毒从感染的tick传播到未感染的tick的共同喂养传播(非病毒传播)。未来的研究应旨在鉴定促进病毒传播的主要壁虱唾液分子,以及壁虱-宿主-病毒相互作用和壁虱介导的皮肤免疫调节的分子描述。这些见解将有助于设计抗design虫疫苗,从而防止由against虫传播的病毒引起的疾病。

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