Tang Zeli, Shang Mei, Chen Tingjin, Ren Pengli, Sun Hengchang, Qu Hongling, Lin Zhipeng, Zhou Lina, Yu Jinyun, Jiang Hongye, Zhou Xinyi, Li Xuerong, Huang Yan, Xu Jin, Yu Xinbing
Department of Parasitology, Zhongshan School of Medicine, Sun Yat-sen University, 74 Zhongshan 2nd Road, Guangzhou, 510080, China.
Key Laboratory for Tropical Diseases Control, Sun Yat-sen University, Ministry of Education, Guangzhou, 510080, Guangdong, China.
Parasit Vectors. 2016 Dec 19;9(1):648. doi: 10.1186/s13071-016-1928-0.
Clonorchiasis, a food-borne zoonosis, is caused by Clonorchis sinensis. The intestinal tract and bile ducts are crucial places for C. sinensis metacercariae to develop into adult worms. The endospore of Bacillus subtilis is an ideal oral immunization vehicle for delivery of heterologous antigens to intestine. Cysteine protease of C. sinensis (CsCP) is an endogenous key component in the excystment of metacercariae and other physiological or pathological processes.
We constructed a fusion gene of CotC (a coat protein)-CsCP and obtained B. subtilis spores with recombinant plasmid of pEB03-CotC-CsCP (B.s-CotC-CsCP). CotC-CsCP expressed on spores' surface was detected by Western blotting and immunofluorescence. Immunological characteristics of recombinant spore coat protein were evaluated in a mouse model. The levels of CsCP-specific antibodies were detected by ELISA. Effects of recombinant spores on mouse intestine were evaluated by histological staining. The activities of biochemical enzymes in serum were assayed by microplate. Liver sections of infected mice were evaluated by Ishak score after Masson's trichrome.
The B.s-CotC-CsCP spores displayed CsCP on their coat. Specific IgG and isotypes were significantly induced by coat proteins of B.s-CotC-CsCP spores after subcutaneous immunization. IgA levels in intestinal mucus and bile of B.s-CotC-CsCP orally treated mice significantly increased. Additionally, more IgA-secreting cells were observed in enteraden and lamina propria regions of the mouse jejunum, and an increased amount of acidic mucins in intestines were also observed. There were no significant differences in enzyme levels of serum among groups. No inflammatory injury was observed in the intestinal tissues of each group. The degree of liver fibrosis was significantly reduced after oral immunization with B.s-CotC-CsCP spores.
Bacillus subtilis spores maintained the original excellent immunogenicity of CsCP expressed on their surface. Both local and systemic specific immune responses were elicited by oral administration of B.s-CotC-CsCP spores. The spores effectively promoted intestinal health by inducing secretion of acidic mucins, with no other side effects to the liver or intestine. Oral administration of spores expressing CsCP could provide effective protection against C. sinensis. This study may be a cornerstone for development of antiparasitic agents or vaccines against clonorchiasis based on B. subtilis spore expressing CsCP on the surface.
华支睾吸虫病是一种食源性人畜共患病,由华支睾吸虫引起。肠道和胆管是华支睾吸虫囊蚴发育为成虫的关键部位。枯草芽孢杆菌的内生孢子是将异源抗原递送至肠道的理想口服免疫载体。华支睾吸虫的半胱氨酸蛋白酶(CsCP)是囊蚴脱囊及其他生理或病理过程中的内源性关键成分。
我们构建了CotC(一种外壳蛋白)-CsCP融合基因,并获得了携带pEB03-CotC-CsCP重组质粒的枯草芽孢杆菌孢子(B.s-CotC-CsCP)。通过蛋白质免疫印迹法和免疫荧光法检测孢子表面表达的CotC-CsCP。在小鼠模型中评估重组孢子外壳蛋白的免疫特性。通过酶联免疫吸附测定法检测CsCP特异性抗体水平。通过组织学染色评估重组孢子对小鼠肠道的影响。通过微孔板检测血清中生化酶的活性。用Masson三色染色法染色后,根据Ishak评分评估感染小鼠的肝脏切片。
B.s-CotC-CsCP孢子在其外壳上展示了CsCP。皮下免疫后,B.s-CotC-CsCP孢子的外壳蛋白显著诱导了特异性IgG和各亚型抗体。口服B.s-CotC-CsCP的小鼠肠道黏液和胆汁中的IgA水平显著升高。此外,在小鼠空肠的肠腺和固有层区域观察到更多分泌IgA的细胞,并且在肠道中也观察到酸性黏蛋白的量增加。各组血清中的酶水平无显著差异。每组的肠道组织均未观察到炎性损伤。口服B.s-CotC-CsCP孢子后,肝纤维化程度显著降低。
枯草芽孢杆菌孢子保持了其表面表达的CsCP原有的优异免疫原性。口服B.s-CotC-CsCP孢子可引发局部和全身特异性免疫反应。孢子通过诱导酸性黏蛋白的分泌有效促进肠道健康,对肝脏或肠道无其他副作用。口服表达CsCP的孢子可为抵抗华支睾吸虫提供有效保护。本研究可能是基于表面表达CsCP的枯草芽孢杆菌孢子开发抗华支睾吸虫病寄生虫药物或疫苗的基石。