期刊文献+

表达猫瘟病毒VP2蛋白重组减毒鼠伤寒沙门菌SL1344ΔcrpΔasd(pYA3493-VP2)构建及特性研究 被引量:1

Construction and characterization of recombinant attenuated Salmonella typhimurium SL1344ΔcrpΔasd(pYA3493)expressing VP2 protein of feline panleukopenia virus
原文传递
导出
摘要 为构建稳定表达猫瘟病毒(FPV)免疫原性蛋白VP2减毒鼠伤寒沙门菌重组菌株,以洛阳分离株基因组为模板扩增VP2基因,并克隆至原核表达载体pYA3493,然后电转化至减毒鼠伤寒沙门菌SL1344ΔcrpΔasd,构建重组菌株SL1344ΔcrpΔasd(pYA3493-VP2),并对其表型及生长特性、遗传稳定性、生物被膜、运动性以及毒力等进行分析。结果显示,携带FPVVP2基因重组减毒沙门菌SL1344ΔcrpΔasd(pYA3493-VP2)重组菌构建成功并表达出外源蛋白;SL1344ΔcrpΔasd(pYA3493-VP2)的生化、生长特性与空载体互补菌SL1344ΔcrpΔasd(pYA3493)相似,较亲本菌株SL1344失去了利用麦芽糖、蔗糖、甘露醇、山梨醇等碳源能力,生长速度、运动性、生物膜形成能力相较亲本株SL1344均发生了显著降低,但小鼠LD50较亲本株提高126倍。结果表明,成功构建了稳定携带FPV VP2蛋白新型减毒鼠伤寒沙门菌SL1344ΔcrpΔasd(pYA3493-VP2),该重组菌能够有效递呈所携带外源基因并稳定表达,为进一步预防FPV感染和新型疫苗研发提供理论依据。 To construct a recombinant strain of Salmonella typhimurium that stably expressed the immunogenic protein VP2 of feline panleukopenia virus(FPV).Firstly,VP2 gene was amplified by using the genome of FPV Luoyang isolate as a template,and cloned into prokaryotic expression vector p YA3493.Then,the recombinant vector p YA3493-VP2 was electrically transformed into Salmonella typhimurium SL1344ΔcrpΔasd and obtained recombinant strain SL1344ΔcrpΔasd(p YA3493-VP2).Lastly,the recombinant strain phenotype,growth characteristics,genetic stability,biofilm,motility and virulence were analyzed.The results showed that recombinant strain SL1344ΔcrpΔasd(p YA3493-VP2)was successfully constructed and expressed foreign protein.The biochemical and growth characteristics of SL1344ΔcrpΔasd(p YA3493-VP2)were similar to those of the empty vector complementary strain SL1344ΔcrpΔasd(p YA3493).Compared with the parental strain SL1344,the strain lost the ability to utilize maltose,sucrose,mannitol,sorbitol and other carbon sources,and its growth rate motility and biofilm formation ability of the recombinant strain were significantly decreased,but the mouse LD50strain was 126 times higher than the parental strain.These results indicated that the novel attenuated Salmonella typhimurium strain SL1344ΔcrpΔasd(p YA3493-VP2)stably carrying FPV VP2 protein was successfully constructed.The recombinant bacteria can effectively present expressionthe foreign genes,which provides a new idea for further prevention of FPV infection and the development of novel vaccines.
作者 王文婕 杜付熙 郁川 尚珂 余祖华 李静 贾艳艳 廖成水 丁轲 张春杰 程相朝 陈松彪 WANG Wen-jie;DU Fu-xi;YU Chuan;SHANG Ke;YU Zu-hua;LI Jing;JIA Yan-yan;LIAO Cheng-shui;DING Ke;ZHANG Chun-jie;CHENG Xiang-chao;CHEN Song-biao(Luoyang Key Laboratory of Live Carrier Biomaterial and Animal Disease Prevention and Control,Luoyang 471003,China;Laboratory of Functional Microbiology and Animal Health,Henan University of Science and Technology,Luoyang 471003,China;Animal Diseases and Public Health Engineering Research Center of Henan Province,Luoyang 471099,China)
出处 《中国兽医科学》 CAS CSCD 北大核心 2023年第2期189-197,共9页 Chinese Veterinary Science
基金 河南科技大学博士研究启动专项基金(13480104) 河南省自然科学基金项目(182300410078)。
关键词 猫瘟病毒 VP2 减毒鼠伤寒沙门菌 特性 feline panleukopenia virus(FPV) VP2 attenuated Salmonella typhimurium characterization
作者简介 共同为第一作者:王文婕(1994-),女,河南鹤壁人,硕士生,E-mail:wangwj_emai1@163.com;共同为第一作者:杜付熙(1998-),男,河南商丘人,硕士生,E-mail:1430553754@qq.com;通讯作者:程相朝(1967-),男,河南汝州人,教授,博士,主要从事动物病理学的研究,E-mail:chengxch@126.com;通讯作者:陈松彪(1990-),男,河南信阳人,讲师,博士,主要从事动物病理学的研究E-mail:chensongbiao@126.com。
  • 相关文献

参考文献4

二级参考文献40

  • 1加春生,毛泽明,耿明杰,王俊峰,王晓楠,王龙,陈爽,葛兰云,徐世文.猪沙门菌分离株的毒力及耐药特征[J].中国兽医科学,2015,45(2):190-194. 被引量:4
  • 2赖文凤,谢建蒙,张建滨,张晓锋,蓝荣彬.松鼠猴病毒性肺炎的诊断和治疗[J].中国兽医杂志,2005,41(3):45-46. 被引量:3
  • 3彭海滨,吴德峰,孔繁德,徐淑菲,陈琼.我国沙门菌污染分布概况[J].中国国境卫生检疫杂志,2006,29(2):125-128. 被引量:53
  • 4徐引弟,郭爱珍,刘维红,贾爱卿,陈焕春.猪霍乱沙门氏菌C500株△crp△asd缺失株平衡致死载体系统的构建及鉴定[J].生物工程学报,2006,22(3):366-372. 被引量:31
  • 5Imberechts H, De Greve H, Lintermans P. The pathogenesis of edema disease in pigs-A review. Veterinary Microbiology, 1992, 31:221 - 233.
  • 6Imberechts H, Wild P, Charlier G, et al. Characterization of F18 fimbrial genes fedE and fedF involved in adhesion and length of enterotoxemic Escherichia coli strain 107/86. Microbial Pathogenesis, 1996, 21 (3) : 183 - 192.
  • 7Moxley RA. Edema disease. Veterinary clinics of North America-Food Animal Practice, 2000, 16(1) : 175 - 185.
  • 8Smeds A, Pertovaara M, Timonen T, et al. Mapping the binding domain of the F18 fimbrial adhesin. Infection and Immunity, 2003, 71(4): 2163-2172.
  • 9Weinstein DL, MP Jackson, JE Samuel, et al. Cloning and sequencing of a Shiga-like toxin type Ⅱ variant from Escherichia coli strain responsible for edema disease of swine. Journal of Bacteriology, 1988, 170(9): 4223-4230.
  • 10Austin PR, Hovde CJ. Purification of recombinant shiga-like toxin type I B subunit. Protein Expression and Purification,1995, 6(6): 771 - 779.

共引文献16

同被引文献9

引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部