期刊文献+

番茄溃疡病菌单克隆抗体的制备与鉴定

Preparation and identification of monoclonal antibodies against the bacterial canker of tomato
在线阅读 下载PDF
导出
摘要 为制备并鉴定番茄溃疡病菌(Clavibacter michiganensis subsp.michiganensis,Cmm)的单克隆抗体(McAbs),用全菌皮下免疫BALB/C小鼠,采用B细胞杂交瘤技术,经免疫、融合、间接ELISA筛选和克隆等,获得稳定分泌抗体的阳性杂交瘤细胞株,得到了抗番茄溃疡病菌的单克隆抗体。经免疫后获得3株单抗分别为1A4、1C3和1B7,经亚类鉴定分别是IgM、IgG1、IgG1;纯化腹水间接ELISA效价分别为1:3.2×106、1:8.1×105、1:3.2×106;与其他同属不同亚种无交叉反应。结果表明:3株单克隆抗体均具有较高特异性和敏感性,可作为番茄溃疡病菌的检测抗体,其中,1A4的效果最好。番茄溃疡病菌单克隆抗体的获得为进一步研发番茄溃疡病检测试剂盒奠定了基础。 To prepare and identify monoclonal antibodies(McAbs) agains Bacterial canker of tomato,Cmm,BALB/C mice were immunized with Cmm hypodermically and McAbs were gained by hybridoma cell lines secreting McAbs were obtained using routine hybridoma technology and ELISA screening.Three hybridoma cell lines specific to Cmm were obtained after screening with indirect ELISA and subcloning.They were designated as 1A4,1C3 and 1B7.Identification of the subclass indicated that the monoclonal antibody secreted by 1A4 cell line belonged to IgM,while those secreted by 1C3 and 1B7 belonged to IgG1.As demonst rated by indirect ELISA,the titers of the purified ascetic fluids of 1A4,1C3,1B7 were 1:3.2×106,1:8.1×105,1:3.2×106,respectively.The McAbs had no cross-reaction with some subspecies of bacteriums.It is evident that these monoclonal antibodies all show high degree of specificity and sensitivity,Which,1A4 was the best.The results show that the specific Cmm McAbs are developed and these McAbs may be useful in the development of detection assay.
出处 《植物检疫》 北大核心 2011年第4期42-46,共5页 Plant Quarantine
基金 甘肃省科技厅中小企业创新基金计划(0802NCCA028) 国家质检总局项目(2007IK259 2009IK276)
关键词 单克隆抗体 番茄溃疡病菌 ELISA monoclonal antibodies Clavibacter michiganensis subsp.michiganensis ELISA
作者简介 通讯作者:E-mail:ciqql@sohu.com
  • 相关文献

参考文献9

  • 1OEPP/EPPO. Clavibacter michiganensis subsp, michiganensis. OE PP/EPPO Bulletin,2005, 35 : 275 -283.
  • 2Luo L X, Waiters C, Li J Q, et al. Quantification of viable cells of Clavibactermichiganensis subsp, michiganensis using a DNA binding dye and a real - time PCR assay. Plant Pathology, 2008. 57 : 332 - 337.
  • 3冯志新,迟灵芝,刘茂军,王海燕,甘源,吴叙苏,邵国青.猪肺炎支原体P46蛋白单克隆抗体制备[J].江苏农业学报,2010,26(2):320-324. 被引量:11
  • 4Robertom C Guedes, Connie J Gebhart. Preparation and characterization of polyclonal and monoclonal antibodies against Lawsonia intracellularis. J Vet Diagn Invest,2003,15:438 - 446.
  • 5Mohammad S, Mohammad A, Maliheh P. Preparation and Characterization of Monoclonal Antibody Against Melatonin. Hybrido- ma,2008,27 ( 3 ) :205 - 209.
  • 6Wang J H, Dun X P, Qu L N. Preparation and Identification of Monoclonal Antibodies Against Pea, Albumin 1 b ( PAl b). Hybridoma,2005,24 (4) : 197 - 200.
  • 7Gold ing J W. Monoclonal antibodies: principles and practice. London, New York : Academic Press, 1993:76 - 77.
  • 8萨姆布鲁克J,拉塞尔DW.分子克隆实验指南.黄培堂,等译.3版.北京:科学出版社,2002.
  • 9Friguet B, Chaffo tte A F, D javadi - Ohaniance L , et al. Measurements of the tree affinity constant in solution of antigene antibody complexes by enzyme - linked immuno so rbent assay. J Immuno 1Methods, 1985, 77: 305.

二级参考文献17

  • 1苏锐,邵国青,张映.猪肺炎支原体P97基因原核表达产物单抗的制备[J].中国人兽共患病杂志,2005,21(3):202-205. 被引量:5
  • 2胡茂志,焦新安,潘志明,邵国青,刘秀梵.抗猪肺炎支原体特异性P36蛋白单克隆抗体的制备与鉴定[J].中国兽医学报,2006,26(6):619-621. 被引量:5
  • 3FUTO S,SETO Y,MITSOSE S,et al.Molecular cloning of a 46 kD surface antigen (P46) gene from Mycoplasma hyopneumoniae:direct evidence of CGG codon usage for argmine[J].J Bacterial,1995,177(7):1917-1919.
  • 4GOLDING J W.Monoclonal antibodies:principles and practice[M].London,New York:Academic Press,1993:76-77.
  • 5MEYLING A.Mycoplasma suipneumoniae and Mycoplasma hyorhinis denostrated in pneumoniae pig lungs by the fluorescent antibody technique[J].Acta Vet Scan,1971,12:137-141.
  • 6ARMSTRONG C H,FREEMAN M I,SANDS-FREEMANN L,et al.Comparison of the enzyme linked immunesorbent assay and the indirect heamagylutionation and complement fixation tests for deterring antibodies to Mycoplasma hyopneumoniae[J].Can J Comp Med,1983,47:464-470.
  • 7PIFER I A,YOUNG T F,PETENATE A,et al.Comparison of complement fixation test and enzyme linked immunosorbent assay for detection of early infection with Mycoplasma hyopneumoniae[J].J Vet Res,1984,45:1122-1126.
  • 8SHDDRAKE R F,GARDONER I A,SANNDERS M M,et al.Serum antibody respoase to Mycoplasma hyopnenmoniae measured by enzymed-linked immunosorbent assay for experimental and natural fection of pigs[J].Aust Vet J,1990,67:39-42.
  • 9CARON J,OUARDANI M,DEA M.Diagnosis and differentiation of Mycoplasma hyopnenmoniae and Mycoplasma hyorhinis infections in pigs by PCR amplification of the p36 and p46 genes[J].Clin Microbiol,2000,3(4):1390-1396.
  • 10SATOSHI F,YASULFIRO S,MUNEORI O,et al.Recombient 46-kilodalton surface antigen (P46) of Mycoptasma hyopneumoniae expressed in Escherichia coli can be used for early specific diagnosis of Mycoplasma pneumoniae of swine by enzyme-linked immunosorbent assay[J].J Cline Micro,1995,33(3):680-683.

共引文献17

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