Abdelgawad Hosny Ahmed, Lian Zhengmin, Yin Yi, Fang Tian, Tian Mingxing, Yu Shengqing
Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences (CAAS), Shanghai 200241, China.
Department of Microbiology and Immunology, Faculty of Veterinary Medicine, Aswan University, Aswan 81528, Egypt.
Vaccines (Basel). 2023 Jul 21;11(7):1273. doi: 10.3390/vaccines11071273.
is the main causative agent for bovine brucellosis. A19 is a widely used vaccine strain to protect cows from infection in China. However, A19 has a similar lipopolysaccharide (LPS) antigen to that of the field virulent strain, whose immunization interferes with the serodiagnosis of vaccinated and infected animals. [Aim] To develop a novel DIVA vaccine candidate.
The mutant A19mut2 with the formyltransferase gene is replaced by an acetyltransferase gene from O157 using the bacterial homologous recombination technique, generating a modified O-polysaccharide that cannot induce antibodies in mice against wild-type LPS. The biological phenotypes of the A19mut2 were assessed using a growth curve analysis, agglutination tests, Western blotting, and stress resistance assays. Histopathological changes and bacterial colonization in the spleens of vaccinated mice were investigated to assess the residual virulence and protection of the A19mut2. Humoral and cellular immunity was evaluated by measuring the levels of IgG, IgG subtypes, and the release of cytokines IFN-γ and IL10 in the splenocytes of the vaccinated mice. ELISA coated with wild-type LPS can distinguish mouse antibodies induced by A19 and A19mut2 immunization.
The A19mut2 showed a decreased residual virulence in mice, compared to the A19 strain, but induced significant humoral and cellular immune responses, as the A19 immunization did. The protection efficacy of A19mut2 immunization against S2308 Nal infection was similar to that of A19 immunization.
The A19mut2 has potential as a novel DIVA vaccine candidate in the future.
是牛布鲁氏菌病的主要病原体。A19是中国广泛用于保护奶牛免受感染的疫苗株。然而,A19具有与田间强毒株相似的脂多糖(LPS)抗原,其免疫会干扰接种疫苗和感染动物的血清学诊断。[目的]开发一种新型的鉴别诊断疫苗候选物。
利用细菌同源重组技术,将A19突变体A19mut2中编码甲酰基转移酶的基因替换为来自O157的乙酰基转移酶基因,产生一种修饰的O-多糖,该多糖不能诱导小鼠产生针对野生型LPS的抗体。使用生长曲线分析、凝集试验、蛋白质印迹和抗逆性试验评估A19mut2的生物学表型。研究接种疫苗小鼠脾脏中的组织病理学变化和细菌定植情况,以评估A19mut2的残余毒力和保护作用。通过测量接种疫苗小鼠脾细胞中IgG、IgG亚型的水平以及细胞因子IFN-γ和IL10的释放来评估体液免疫和细胞免疫。用野生型LPS包被的ELISA可区分由A19和A19mut2免疫诱导的小鼠抗体。
与A19菌株相比,A19mut2在小鼠中的残余毒力降低,但与A19免疫一样,能诱导显著的体液免疫和细胞免疫反应。A19mut2免疫对S2308 Nal感染的保护效果与A19免疫相似。
A19mut2未来有潜力作为一种新型的鉴别诊断疫苗候选物。