ICAR-National Institute of Veterinary Epidemiology and Disease Informatics (NIVEDI), Post Box No. 6450, Yelahanka, Bengaluru, 560064, Karnataka, India.
ICAR-Krishi Vigyan Kendra (KVK), ICAR-Research Complex for NEH Region, Hailakandi, 788152, Assam, India.
Anaerobe. 2024 Oct;89:102899. doi: 10.1016/j.anaerobe.2024.102899. Epub 2024 Aug 12.
Flagellin protein, an integral component of flagella, provides motility to several bacterial species and also acts as a candidate antigen in diagnostics and subunit vaccines. The bulk production of flagellin with retention of all conformational epitopes using recombinant protein technology is of paramount importance in the development of pathogen-specific immuno-assays and vaccines. We describe the production of highly soluble and immuno-reactive rFliA(C) protein of Clostridium chauvoei, a causative agent of blackleg or black quarter (BQ) affecting cattle and small ruminants worldwide. The bacterium is known to possess peritrichous flagella that provide motility and also act as a virulence factor with high protective antigenicity.
Upon sequence and structural analysis, a partial fliA(C) gene from Clostridium chauvoei was cloned and the recombinant mature protein with N- and C- terminal truncation was over-expressed as a His-tagged fusion protein (∼25 kDa) in Escherichia coli. Subsequently, rFliA(C) protein was purified by single-step affinity chromatography and characterized for its immuno-reactivity in laboratory animals, Western blot, and indirect-ELISA format.
rFliA(C) was highly soluble and was purified in high quantity and quality. rFliA(C) elicited antigen-specific conformational polyclonal antibodies in rabbit and guinea pig models, as well as anti-Clostridium chauvoei-specific antibodies being specifically detected in BQ-vaccinated and convalescent sera of bovines in Western blot and in indirect-ELISA format. Further, no cross reactivity was noted with antibodies against major bovine diseases (e.g., foot-and-mouth disease, IBR, LSDV, hemorrhagic septicaemia, brucellosis, and leptospirosis).
The study indicated the production of conformational recombinant flagellin-rFliA(C)-antigen and its potential utility in development of diagnostics for detection of Clostridium chauvoei-specific antibodies in BQ-recovered and/or vaccinated animals.
鞭毛蛋白是鞭毛的组成部分,为几种细菌提供运动能力,也作为诊断和亚单位疫苗中的候选抗原。使用重组蛋白技术大量生产保留所有构象表位的鞭毛蛋白对于开发针对病原体的免疫测定和疫苗至关重要。我们描述了使用重组蛋白技术生产 highly soluble 和 immuno-reactive rFliA(C)蛋白,该蛋白来自 Clostridium chauvoei,是一种引起黑腿或黑 quarter (BQ)的病原体,影响全球的牛和小反刍动物。已知该细菌具有周生鞭毛,可提供运动能力,并且作为一种具有高保护性抗原性的毒力因子。
经过序列和结构分析,从 Clostridium chauvoei 克隆了部分 fliA(C)基因,并在大肠杆菌中表达了带有 N-和 C-末端截断的重组成熟蛋白作为 His 标记融合蛋白(约 25 kDa)。随后,通过单步亲和层析纯化 rFliA(C)蛋白,并在实验室动物、Western blot 和间接 ELISA 中对其免疫反应性进行了表征。
rFliA(C)高度可溶性,可高质量、高产量纯化。rFliA(C)在兔和豚鼠模型中诱导抗原特异性构象多克隆抗体,并且在 BQ 疫苗接种和牛的恢复期血清中特异性检测到针对 Clostridium chauvoei 的特异性抗体,Western blot 和间接 ELISA 中均如此。此外,与针对主要牛病(例如口蹄疫、IBR、LSDV、出血性败血症、布鲁氏菌病和钩端螺旋体病)的抗体无交叉反应。
该研究表明生产了构象重组鞭毛蛋白-rFliA(C)-抗原,并且其在开发针对 BQ 恢复和/或接种动物中检测 Clostridium chauvoei 特异性抗体的诊断方法中具有潜在用途。