Leal-Galvan Brenda, Kumar Deepak, Karim Shahid, Saelao Perot, Thomas Donald B, Oliva Chavez Adela
Department of Entomology, Texas A&M University, College Station, TX, United States.
USDA-ARS Cattle Fever Tick Research Laboratory, Edinburg, TX, United States.
Front Cell Dev Biol. 2024 Sep 23;12:1460705. doi: 10.3389/fcell.2024.1460705. eCollection 2024.
Ticks are important blood feeding ectoparasites that transmit pathogens to wildlife, domestic animals, and humans. Hard ticks can feed for several days to weeks, nevertheless they often go undetected. This phenomenon can be explained by a tick's ability to release analgesics, immunosuppressives, anticoagulants, and vasodilators within their saliva. Several studies have identified extracellular vesicles (EVs) as carriers of some of these effector molecules. Further, EVs, and their contents, enhance pathogen transmission, modulate immune responses, and delay wound healing. EVs are double lipid-membrane vesicles that transport intracellular cargo, including microRNAs (miRNAs) to recipient cells. miRNAs are involved in regulating gene expression post-transcriptionally. Interestingly, tick-derived miRNAs have been shown to enhance pathogen transmission and affect vital biological processes such as oviposition, blood digestion, and molting. miRNAs have been found within tick salivary EVs. This review focuses on current knowledge of miRNA loading into EVs and homologies reported in ticks. We also describe findings in tick miRNA profiles, including miRNAs packed within tick salivary EVs. Although no functional studies have been done to investigate the role of EV-derived miRNAs in tick feeding, we discuss the functional characterization of miRNAs in tick biology and pathogen transmission. Lastly, we propose the possible uses of tick miRNAs to develop management tools for tick control and to prevent pathogen transmission. The identification and functional characterization of conserved and tick-specific salivary miRNAs targeting important molecular and immunological pathways within the host could lead to the discovery of new therapeutics for the treatment of tick-borne and non-tick-borne human diseases.
蜱是重要的吸血外寄生虫,可将病原体传播给野生动物、家畜和人类。硬蜱可以吸食数天至数周,但它们常常未被发现。这种现象可以用蜱在唾液中释放止痛剂、免疫抑制剂、抗凝血剂和血管扩张剂的能力来解释。多项研究已确定细胞外囊泡(EVs)是其中一些效应分子的载体。此外,EVs及其内含物可增强病原体传播、调节免疫反应并延缓伤口愈合。EVs是双层脂质膜囊泡,可将包括微小RNA(miRNAs)在内的细胞内物质运输到受体细胞。miRNAs参与转录后基因表达的调控。有趣的是,已证明蜱源miRNAs可增强病原体传播,并影响产卵、血液消化和蜕皮等重要生物学过程。在蜱唾液EVs中发现了miRNAs。本综述重点关注目前关于miRNAs装载到EVs中的知识以及蜱中报道的同源性。我们还描述了蜱miRNA谱的研究结果,包括蜱唾液EVs中包裹的miRNAs。尽管尚未进行功能研究来调查EV衍生的miRNAs在蜱进食中的作用,但我们讨论了miRNAs在蜱生物学和病原体传播中的功能特征。最后,我们提出蜱miRNAs在开发蜱控制管理工具和预防病原体传播方面的可能用途。鉴定和功能表征靶向宿主内重要分子和免疫途径的保守和蜱特异性唾液miRNAs,可能会发现治疗蜱传和非蜱传人类疾病的新疗法。