Department of Veterinary Microbiology and Pathology, Washington State University, Pullman, WA, USA.
Animal Disease Research Unit, Agricultural Research Service (ARS), U.S. Department of Agriculture, Pullman, WA, USA.
Parasit Vectors. 2023 Jan 17;16(1):16. doi: 10.1186/s13071-022-05628-6.
Babesia bovis, an intra-erythrocytic apicomplexan parasite, is one of the causative agents of bovine babesiosis, the most important tick-borne disease of cattle in tropical and subtropical regions. Babesia bovis has a complex life-cycle that includes sexual development within the tick vector. The development of a transmission blocking vaccine to control bovine babesiosis requires the identification of antigens displayed on the surface of the parasite during its development within tick vectors. Four B. bovis cysteine-rich GCC2/GCC3 domain protein (BboGDP) family members were previously identified and are differentially expressed as discrete pairs by either blood stages or kinetes. In this study we focused on two family members, BboGDP1 and -3, that are expressed by Babesia parasites during tick infection. METHODS AND RESULTS: Transcription analysis using quantitative PCR demonstrated that BboGDP1 and -3 were upregulated in in vitro-induced sexual stage parasites and during parasite development in the tick midgut. Moreover, protein expression analysis of BboGDP1 and -3 during the development of sexual stages in in vitro culture was consistent with their transcription profile. Live immunofluorescence analysis using polyclonal antibodies confirmed surface expression of BboGDP1 and -3 on in vitro-induced sexual stage parasites. In addition, fixed immunofluorescence analysis showed reactivity of anti-BboGDP1 and -3 polyclonal antibodies to kinetes.
The collective data indicate that BboGDP1 and -3 are expressed by kinetes and on the surface of sexual stages of the parasites. The identified parasite surface membrane proteins BboGDP1 and -3 are potential candidates for the development of a B. bovis transmission blocking vaccine.
巴贝斯虫(Babesia bovis)是一种红细胞内顶复门寄生虫,是热带和亚热带地区牛最主要的蜱传疾病——牛巴贝斯虫病的病原体之一。巴贝斯虫具有复杂的生命周期,包括在蜱媒介内的有性发育。为了开发一种用于控制牛巴贝斯虫病的传播阻断疫苗,需要鉴定在寄生虫在蜱媒介内发育过程中显示在表面的抗原。先前已经鉴定出 4 种巴贝斯虫富含半胱氨酸的 GCC2/GCC3 结构域蛋白(BboGDP)家族成员,它们通过血液阶段或动基体以离散对的形式差异表达。在本研究中,我们重点关注了在蜱感染期间由巴贝斯虫寄生虫表达的两个家族成员,BboGDP1 和 -3。
使用定量 PCR 的转录分析表明,BboGDP1 和 -3 在体外诱导的有性阶段寄生虫中和在蜱中肠内寄生虫发育过程中上调。此外,BboGDP1 和 -3 在体外培养的有性阶段发育过程中的蛋白表达分析与它们的转录谱一致。使用多克隆抗体的活体免疫荧光分析证实了 BboGDP1 和 -3 在体外诱导的有性阶段寄生虫表面的表达。此外,固定免疫荧光分析显示抗-BboGDP1 和 -3 多克隆抗体对动基体的反应性。
这些综合数据表明,BboGDP1 和 -3 由动基体和寄生虫有性阶段的表面表达。鉴定出的寄生虫表面膜蛋白 BboGDP1 和 -3 是开发 B. bovis 传播阻断疫苗的潜在候选物。