{"title":"生产高溶解性和免疫反应性重组潮气荚膜梭菌鞭毛蛋白。","authors":"Awadhesh Prajapati , Roopa Anandamurthy Hemanth , Mandira Ramakrishna Namrutha , Suresh Bindu , Revanaiah Yogisharadhya , Nihar Nalini Mohanty , Mohammed Mudassar Chanda , Sathish Bhadravati Shivachandra","doi":"10.1016/j.anaerobe.2024.102899","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><p>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 <em>Clostridium chauvoei,</em> 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.</p></div><div><h3>Methods</h3><p>Upon sequence and structural analysis, a partial <em>fliA(C)</em> gene from <em>Clostridium chauvoei</em> 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 <em>Escherichia coli</em>. 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.</p></div><div><h3>Results</h3><p>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-<em>Clostridium chauvoei-</em>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).</p></div><div><h3>Conclusion</h3><p>The study indicated the production of conformational recombinant flagellin—rFliA(C)—antigen and its potential utility in development of diagnostics for detection of <em>Clostridium chauvoei-</em>specific antibodies in BQ-recovered and/or vaccinated animals.</p></div>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Production of highly soluble and immuno-reactive recombinant flagellin protein of Clostridium chauvoei\",\"authors\":\"Awadhesh Prajapati , Roopa Anandamurthy Hemanth , Mandira Ramakrishna Namrutha , Suresh Bindu , Revanaiah Yogisharadhya , Nihar Nalini Mohanty , Mohammed Mudassar Chanda , Sathish Bhadravati Shivachandra\",\"doi\":\"10.1016/j.anaerobe.2024.102899\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Objective</h3><p>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 <em>Clostridium chauvoei,</em> 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.</p></div><div><h3>Methods</h3><p>Upon sequence and structural analysis, a partial <em>fliA(C)</em> gene from <em>Clostridium chauvoei</em> 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 <em>Escherichia coli</em>. 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.</p></div><div><h3>Results</h3><p>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-<em>Clostridium chauvoei-</em>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).</p></div><div><h3>Conclusion</h3><p>The study indicated the production of conformational recombinant flagellin—rFliA(C)—antigen and its potential utility in development of diagnostics for detection of <em>Clostridium chauvoei-</em>specific antibodies in BQ-recovered and/or vaccinated animals.</p></div>\",\"PeriodicalId\":2,\"journal\":{\"name\":\"ACS Applied Bio Materials\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2024-08-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Bio Materials\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1075996424000829\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, BIOMATERIALS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1075996424000829","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 0
摘要
目的:鞭毛蛋白是鞭毛的一个组成部分,它为多种细菌提供运动能力,也是诊断和亚单位疫苗的候选抗原。利用重组蛋白技术批量生产能保留所有构象表位的鞭毛蛋白,对于开发病原体特异性免疫测定和疫苗至关重要。我们描述了高可溶性和免疫反应性 rFliA(C)梭菌蛋白的生产过程,梭菌是影响全球牛和小反刍动物的黑腿病(BQ)的致病菌。众所周知,该细菌具有富周鞭毛,可提供运动能力,同时也是一种具有高度保护性抗原性的毒力因子:方法:通过序列和结构分析,克隆了来自 Chauvoei梭菌的部分 fliA(C) 基因,并在大肠杆菌中过度表达了 N 端和 C 端截断的重组成熟蛋白,即 His 标记的融合蛋白(25 kDa)。结果:rFliA(C)具有很高的可溶性,纯化的数量和质量都很高。rFliA(C)能在家兔和豚鼠模型中激发抗原特异性构象多克隆抗体,并能在接种过 BQ 疫苗的牛和恢复期牛的血清中通过 Western 印迹和间接-ELISA 方法特异性地检测到抗梭状芽孢杆菌特异性抗体。此外,与主要牛病(如口蹄疫、IBR、LSDV、出血性败血症、布鲁氏菌病和钩端螺旋体病)的抗体没有交叉反应:该研究表明,重组鞭毛蛋白-rFliA(C)-抗原的制备及其在开发用于检测BQ恢复和/或疫苗接种动物体内梭状芽孢杆菌特异性抗体的诊断中的潜在用途。
Production of highly soluble and immuno-reactive recombinant flagellin protein of Clostridium chauvoei
Objective
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.
Methods
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.
Results
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).
Conclusion
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.