Department of Entomology, Texas A&M University, College Station, TX, 77843-2475, USA.
Knipling-Bushland U.S. Livestock Insects Research Laboratory and Veterinary Pest Genomics Center, United States Department of Agriculture-Agricultural Research Service (USDA-ARS), 2700 Fredericksburg Road, Kerrville, TX, 78028-9184, USA.
Parasit Vectors. 2022 Jul 11;15(1):252. doi: 10.1186/s13071-022-05349-w.
Rhipicephalus microplus is the vector of deadly cattle pathogens, especially Babesia spp., for which a recombinant vaccine is not available. Therefore, disease control depends on tick vector control. However, R. microplus populations worldwide have developed resistance to available acaricides, prompting the search for novel acaricide targets. G protein-coupled receptors (GPCRs) are involved in the regulation of many physiological processes and have been suggested as druggable targets for the control of arthropod vectors. Arthropod-specific signaling systems of small neuropeptides are being investigated for this purpose. The pyrokinin receptor (PKR) is a GPCR previously characterized in ticks. Myotropic activity of pyrokinins in feeding-related tissues of Rhipicephalus sanguineus and Ixodes scapularis was recently reported.
The R. microplus pyrokinin receptor (Rhimi-PKR) was silenced through RNA interference (RNAi) in female ticks. To optimize RNAi, a dual-luciferase assay was applied to determine the silencing efficiency of two Rhimi-PKR double-stranded RNAs (dsRNA) prior to injecting dsRNA in ticks to be placed on cattle. Phenotypic variables of female ticks obtained at the endpoint of the RNAi experiment were compared to those of control female ticks (non-injected and beta-lactamase dsRNA-injected). Rhimi-PKR silencing was verified by quantitative reverse-transcriptase PCR in whole females and dissected tissues.
The Rhimi-PKR transcript was expressed in all developmental stages. Rhimi-PKR silencing was confirmed in whole ticks 4 days after injection, and in the tick carcass, ovary and synganglion 6 days after injection. Rhimi-PKR silencing was associated with an increased mortality and decreased weight of both surviving females and egg masses (P < 0.05). Delays in repletion, pre-oviposition and incubation periods were observed (P < 0.05).
Rhimi-PKR silencing negatively affected female reproductive fitness. The PKR appears to be directly or indirectly associated with the regulation of female feeding and/or reproductive output in R. microplus. Antagonists of the pyrokinin signaling system could be explored for tick control.
璃眼蜱是致命牛病原体的传播媒介,特别是巴贝斯虫属,目前尚无针对该病原体的重组疫苗。因此,疾病控制依赖于蜱的控制。然而,全世界的璃眼蜱种群对现有杀蜱剂已经产生了抗药性,这促使人们寻找新的杀蜱剂靶标。G 蛋白偶联受体(GPCR)参与许多生理过程的调节,被认为是控制节肢动物传播媒介的有前途的药物靶点。为此,正在研究小神经肽的节肢动物特异性信号系统。先前已在蜱中鉴定出的发热肽受体(PKR)是一种 GPCR。最近报道了发热肽在 Rhipicephalus sanguineus 和 Ixodes scapularis 与摄食相关的组织中的肌动活性。
通过 RNA 干扰(RNAi)沉默雌性璃眼蜱中的 R. microplus 发热肽受体(Rhimi-PKR)。为了优化 RNAi,应用双荧光素酶测定法来确定两种 Rhimi-PKR 双链 RNA(dsRNA)的沉默效率,然后再将 dsRNA 注射到要放置在牛身上的蜱中。在 RNAi 实验的终点获得的雌性蜱的表型变量与对照雌性蜱(未注射和β-内酰胺酶 dsRNA 注射)进行比较。通过定量逆转录 PCR 在整个雌性和解剖组织中验证 Rhimi-PKR 沉默。
Rhimi-PKR 转录本在所有发育阶段均有表达。注射后 4 天,在整个蜱中以及注射后 6 天在蜱残骸、卵巢和交感神经节中均确认 Rhimi-PKR 沉默。Rhimi-PKR 沉默与死亡率增加和存活雌性和卵团的体重降低有关(P < 0.05)。观察到再补充、产卵前和孵化期的延迟(P < 0.05)。
Rhimi-PKR 沉默对雌性生殖适应性产生负面影响。PKR 似乎直接或间接与 R. microplus 雌性摄食和/或生殖输出的调节有关。发热肽信号系统的拮抗剂可用于蜱的控制。