Pérez-Sánchez Ricardo, Manzano-Román Raúl, Obolo-Mvoulouga Prosper, Oleaga Ana
Parasitología Animal, Instituto de Recursos Naturales y Agrobiología de Salamanca (IRNASA, CSIC), Cordel de Merinas, 40-52, 37008 Salamanca, Spain.
Vet Parasitol. 2019 Aug;272:1-12. doi: 10.1016/j.vetpar.2019.06.016. Epub 2019 Jun 28.
The identification of candidate protective antigens for the development of tick vaccines may be approached by selecting antigen candidates that play key biological functions. Tick midgut proteins that play essential functions in tick survival and disease transmission are upregulated in response to blood feeding and digestion. In this study, Ornithodoros erraticus midgut transcriptomic and proteomic data upon feeding were inspected to select functionally relevant antigens to be assessed as vaccine candidate antigens. For this, we primarily focused on proteins with relevant biological functions in key physiological processes for ticks and tick-host-pathogen interactions. Later, we used additional criteria based on overexpression after feeding, predicted antigenicity and cellular localisation, resulting in the selection of four theoretical candidates, two aquaporins (OeAQP, OeAQP1), one ABC transporter (OeABC) and one selenoprotein T (OeSEL). Rabbit vaccination with synthetic immunogenic peptides designed from the extracellular antigenic regions of the selected candidates induced humoral responses that reduced tick feeding and reproduction performance. Both AQPs and OeSEL demonstrated significant protection efficacy against the homologous species O. erraticus, but lower non-significant cross-species protection against Ornithodoros moubata. Conversely, OeABC showed no protection against the homologous species O. erraticus, but significant cross-species protection against O. moubata. These results are the first demonstration of the protective potential of argasid aquaporins, suggesting that they might be included in vaccines for the control of multiple tick species. Additionally, these results also unveiled two novel protective antigens from argasid ticks, OeABC and OeSEL, belonging to functional protein families that have never been explored as a source of vaccine candidates and are deserving of further studies. Finally, our data add value to the midgut as a protective candidate antigen source in argasids for the control of tick infestations.
蜱虫疫苗开发中候选保护性抗原的鉴定可通过选择发挥关键生物学功能的抗原候选物来实现。在蜱虫生存和疾病传播中起重要作用的蜱虫中肠蛋白会在取食和消化过程中上调。在本研究中,对饱血后的多变钝缘蜱中肠转录组和蛋白质组数据进行了检查,以选择功能相关的抗原作为疫苗候选抗原进行评估。为此,我们主要关注在蜱虫关键生理过程以及蜱 - 宿主 - 病原体相互作用中具有相关生物学功能的蛋白质。随后,我们基于饱血后的过表达、预测的抗原性和细胞定位等额外标准,最终选择了四个理论候选物,即两个水通道蛋白(OeAQP、OeAQP1)、一个ABC转运蛋白(OeABC)和一个硒蛋白T(OeSEL)。用从所选候选物的细胞外抗原区域设计的合成免疫原性肽对兔子进行免疫接种,诱导了体液免疫反应,从而降低了蜱虫的取食和繁殖性能。两种水通道蛋白和OeSEL对同源物种多变钝缘蜱均表现出显著的保护效果,但对莫氏钝缘蜱的跨物种保护效果较低且不显著。相反,OeABC对同源物种多变钝缘蜱没有保护作用,但对莫氏钝缘蜱有显著的跨物种保护作用。这些结果首次证明了argasid水通道蛋白的保护潜力,表明它们可能被纳入用于控制多种蜱虫物种的疫苗中。此外,这些结果还揭示了来自argasid蜱的两种新型保护性抗原,即OeABC和OeSEL,它们属于从未被探索作为疫苗候选物来源的功能蛋白家族,值得进一步研究。最后,我们的数据为中肠作为argasid蜱中用于控制蜱虫侵袭的保护性候选抗原来源增添了价值。