Xian Jinwen, Zhao Pengpeng, Wang Ning, Wang Weiye, Zhang Yanyan, Meng Jimeng, Ma Xun, Wang Zhengrong, Bo Xinwen
State Key Laboratory of Sheep Genetic Improvement and Healthy Production/Institute of Animal Husbandry and Veterinary Medicine, Xinjiang Academy of Agricultural and Reclamation Sciences, Shihezi, China.
College of Animal Science and Technology, Shihezi University, Shihezi, China.
Front Vet Sci. 2021 Nov 17;8:759283. doi: 10.3389/fvets.2021.759283. eCollection 2021.
Cystic echinococcosis (CE) is a cosmopolitan zoonosis caused by the larval stage of , which affects humans and a wide range of mammalian intermediate hosts. Parasite tetraspanin proteins are crucial for host-parasite interactions, and therefore they may be useful for vaccine development or disease diagnosis. In the present study, the major antigen coding sequence of tetraspanin 11 (Eg-TSP11) from was determined. The results of immunolocalization showed that Eg-TSP11 was mainly located in the tegument of adult worms and protoscoleces. Western blotting analysis showed that the serum from dogs injected with recombinant Eg-TSP11 (rEg-TSP11) could recognize Eg-TSP11 among natural protoscolex proteins. Moreover, the serum from dogs with infection also recognized rEg-TSP11. Serum indirect enzyme-linked immunosorbent assays demonstrated that IgG levels gradually increased after the first immunization with rEg-TSP11 compared with those in the control group. Furthermore, the serum levels of interleukin 4, interleukin 5, and interferon gamma were significantly altered in the rEg-TSP11 group. Importantly, we found that vaccination with rEg-TSP11 significantly decreased worm burden and inhibited segment development in a dog model of infection. Based on these findings, we speculated that rEg-TSP11 might be a potential candidate vaccine antigen against infection in dogs.
囊型包虫病(CE)是一种由[具体寄生虫名称]幼虫阶段引起的世界性人畜共患病,可感染人类及多种哺乳动物中间宿主。寄生虫四跨膜蛋白对于宿主 - 寄生虫相互作用至关重要,因此它们可能对疫苗开发或疾病诊断有用。在本研究中,确定了来自[具体寄生虫名称]的四跨膜蛋白11(Eg - TSP11)的主要抗原编码序列。免疫定位结果表明,Eg - TSP11主要位于成虫和原头节的皮层。蛋白质印迹分析表明,注射重组Eg - TSP11(rEg - TSP11)的犬血清能够在天然原头节蛋白中识别Eg - TSP11。此外,感染[具体寄生虫名称]的犬血清也能识别rEg - TSP11。血清间接酶联免疫吸附测定表明,与对照组相比,首次用rEg - TSP11免疫后IgG水平逐渐升高。此外,rEg - TSP11组中白细胞介素4、白细胞介素5和干扰素γ的血清水平发生了显著变化。重要的是,我们发现在[具体寄生虫名称]感染的犬模型中,用rEg - TSP11疫苗接种可显著降低虫负荷并抑制节片发育。基于这些发现,我们推测rEg - TSP11可能是犬抗[具体寄生虫名称]感染的潜在候选疫苗抗原。