Department of Veterinary Pathobiology, College of Veterinary Medicine, Texas A&M University, College Station, Texas, United States of America.
Centro de Biotecnologia, Universidade Federal do Rio Grande do Sul, Porto Alegre, Rio Grande do Sul, Brazil.
PLoS Negl Trop Dis. 2020 Feb 12;14(2):e0007758. doi: 10.1371/journal.pntd.0007758. eCollection 2020 Feb.
Amblyomma americanum ticks transmit more than a third of human tick-borne disease (TBD) agents in the United States. Tick saliva proteins are critical to success of ticks as vectors of TBD agents, and thus might serve as targets in tick antigen-based vaccines to prevent TBD infections. We describe a systems biology approach to identify, by LC-MS/MS, saliva proteins (tick = 1182, rabbit = 335) that A. americanum ticks likely inject into the host every 24 h during the first 8 days of feeding, and towards the end of feeding. Searching against entries in GenBank grouped tick and rabbit proteins into 27 and 25 functional categories. Aside from housekeeping-like proteins, majority of tick saliva proteins belong to the tick-specific (no homology to non-tick organisms: 32%), protease inhibitors (13%), proteases (8%), glycine-rich proteins (6%) and lipocalins (4%) categories. Global secretion dynamics analysis suggests that majority (74%) of proteins in this study are associated with regulating initial tick feeding functions and transmission of pathogens as they are secreted within 24-48 h of tick attachment. Comparative analysis of the A. americanum tick saliva proteome to five other tick saliva proteomes identified 284 conserved tick saliva proteins: we speculate that these regulate critical tick feeding functions and might serve as tick vaccine antigens. We discuss our findings in the context of understanding A. americanum tick feeding physiology as a means through which we can find effective targets for a vaccine against tick feeding.
美洲钝眼蜱传播了美国三分之一以上的人类蜱传疾病(TBD)病原体。蜱唾液蛋白对于蜱作为 TBD 病原体的传播媒介的成功至关重要,因此可能成为基于蜱抗原的疫苗中的靶点,以预防 TBD 感染。我们描述了一种系统生物学方法,通过 LC-MS/MS 鉴定出 A. americanum 蜱在最初 8 天的吸血过程中每 24 小时以及接近吸血末期时可能注入宿主的唾液蛋白(蜱 = 1182,兔 = 335)。在 GenBank 中进行的搜索将蜱和兔的蛋白质分类为 27 个和 25 个功能类别。除了管家样蛋白外,大多数蜱唾液蛋白属于蜱特异性(与非蜱生物无同源性:32%)、蛋白酶抑制剂(13%)、蛋白酶(8%)、富含甘氨酸的蛋白(6%)和脂联素(4%)类别。全局分泌动力学分析表明,本研究中的大多数蛋白质(74%)与调节初始蜱吸血功能和病原体传播有关,因为它们在蜱附着后的 24-48 小时内被分泌。与其他五种蜱唾液蛋白质组的 A. americanum 蜱唾液蛋白质组的比较分析确定了 284 种保守的蜱唾液蛋白质:我们推测这些蛋白质调节着关键的蜱吸血功能,并且可能作为蜱疫苗抗原。我们在理解 A. americanum 蜱吸血生理学的背景下讨论我们的发现,这是我们寻找针对蜱吸血的有效疫苗靶点的一种手段。