Patton Toni G, Dietrich Gabrielle, Brandt Kevin, Dolan Marc C, Piesman Joseph, Gilmore Robert D
Microbiology and Pathogenesis Activity, Bacterial Diseases Branch, Division of Vector-Borne Diseases, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention.
J Vis Exp. 2012 Feb 21(60):3894. doi: 10.3791/3894.
Ticks are found worldwide and afflict humans with many tick-borne illnesses. Ticks are vectors for pathogens that cause Lyme disease and tick-borne relapsing fever (Borrelia spp.), Rocky Mountain Spotted fever (Rickettsia rickettsii), ehrlichiosis (Ehrlichia chaffeensis and E. equi), anaplasmosis (Anaplasma phagocytophilum), encephalitis (tick-borne encephalitis virus), babesiosis (Babesia spp.), Colorado tick fever (Coltivirus), and tularemia (Francisella tularensis) (1-8). To be properly transmitted into the host these infectious agents differentially regulate gene expression, interact with tick proteins, and migrate through the tick (3,9-13). For example, the Lyme disease agent, Borrelia burgdorferi, adapts through differential gene expression to the feast and famine stages of the tick's enzootic cycle (14,15). Furthermore, as an Ixodes tick consumes a bloodmeal Borrelia replicate and migrate from the midgut into the hemocoel, where they travel to the salivary glands and are transmitted into the host with the expelled saliva (9,16-19). As a tick feeds the host typically responds with a strong hemostatic and innate immune response (11,13,20-22). Despite these host responses, I. scapularis can feed for several days because tick saliva contains proteins that are immunomodulatory, lytic agents, anticoagulants, and fibrinolysins to aid the tick feeding (3,11,20,21,23). The immunomodulatory activities possessed by tick saliva or salivary gland extract (SGE) facilitate transmission, proliferation, and dissemination of numerous tick-borne pathogens (3,20,24-27). To further understand how tick-borne infectious agents cause disease it is essential to dissect actively feeding ticks and collect tick saliva. This video protocol demonstrates dissection techniques for the collection of hemolymph and the removal of salivary glands from actively feeding I. scapularis nymphs after 48 and 72 hours post mouse placement. We also demonstrate saliva collection from an adult female I. scapularis tick.
蜱虫遍布全球,可使人类感染多种蜱传疾病。蜱虫是多种病原体的传播媒介,这些病原体可导致莱姆病、蜱传回归热(疏螺旋体属)、落基山斑疹热(立氏立克次体)、埃里希氏体病(查菲埃里希氏体和马埃里希氏体)、无形体病(嗜吞噬细胞无形体)、脑炎(蜱传脑炎病毒)、巴贝斯虫病(巴贝斯虫属)、科罗拉多蜱传热(科蒂病毒)和兔热病(土拉弗朗西斯菌)(1 - 8)。为了能成功传播到宿主体内,这些感染因子会以不同方式调节基因表达、与蜱虫蛋白相互作用并在蜱虫体内迁移(3,9 - 13)。例如,莱姆病病原体伯氏疏螺旋体通过差异基因表达来适应蜱虫生态循环中的饱血期和饥饿期(14,15)。此外,当硬蜱吸食血液时,伯氏疏螺旋体会进行复制并从中肠迁移到血腔,然后到达唾液腺,并随着排出的唾液传播到宿主体内(9,16 - 19)。当蜱虫叮咬时,宿主通常会产生强烈的止血和先天性免疫反应(11,13,20 - 22)。尽管有这些宿主反应,但肩突硬蜱仍能叮咬数天,因为蜱虫唾液中含有免疫调节蛋白、溶解剂、抗凝剂和纤维蛋白溶解酶,有助于蜱虫进食(3,11,20,21,23)。蜱虫唾液或唾液腺提取物(SGE)所具有的免疫调节活性有助于多种蜱传病原体的传播、增殖和扩散(3,20,24 - 27)。为了进一步了解蜱传感染因子如何引发疾病,解剖正在进食的蜱虫并收集蜱虫唾液至关重要。本视频方案展示了在将小鼠放置于蜱虫身上48小时和72小时后,从正在进食的肩突硬蜱若虫中收集血淋巴以及摘除唾液腺的解剖技术。我们还展示了从成年雌性肩突硬蜱中收集唾液的方法。