期刊文献+

脉冲场凝胶电泳技术在猪链球菌分型中的应用 被引量:5

Application of Pulsed Field Gel Electrophoresis in Classification of Streptococcus suis
下载PDF
导出
摘要 脉冲场凝胶电泳是一种可用于分离20 kb至10 Mb大分子质量DNA的新型凝胶电泳技术。该法应用于猪链球菌的分子分型,通过观察电泳条带的差异,为确定菌株之间的亲缘关系,分析基因型和临床症状之间的关系等方面提供了可靠的技术手段。文章介绍了脉冲场凝胶电泳技术的应用状况及猪链球菌的分型现状,并阐述了该技术在猪链球菌分子分型研究方面的应用及发展前景。 Pulsed Field Gel Electrophoresis (PFGE) is a new technique of gel electrophoresis which can be used to separate large DNA molecules ranging from 20 kb to 10 Mb. It has been widely applied to the karyotype analysis and karyotype polymorphism for various bacterium. It applies in the genetic classification of Streptococcus suis to reveal discrimination among different strains and analyses the relation between genotype and clinical symptom through observing the patterns of restriction fragment. In this paper, based on the introduction of the principle of PFGE, the classification of Streptococcus suis, the application and development of PFGE in the research of genetic classification of Streptococcus suis were discussed.
出处 《动物医学进展》 CSCD 2008年第1期70-73,共4页 Progress In Veterinary Medicine
关键词 脉冲场凝胶电泳 猪链球菌 基因分型 应用 PFGE Streptococcus suis ; genetic classification; development
  • 相关文献

参考文献18

  • 1斯特劳 B E,阿莱尔 S D.猪病学[M].8版.北京:中国农业大学出版社,2000:447.
  • 2蔡振鸿,范伟兴,赵冉,何海权,王幼明,姜平,李晓成,黄保续.3个猪链球菌2型四川分离株4个毒力因子基因序列测定与分析[J].中国人兽共患病学报,2006,22(10):901-905. 被引量:5
  • 3付英梅,马佳毓,赵月辉,李蓉.脉冲凝胶电泳技术在细菌学上的应用[J].中国卫生检验杂志,1999,9(1):72-74. 被引量:9
  • 4Sonntag A K,Prager R,Bielaszewska M,et al.Phenotypic and Genotypic Analyses of Enterohemorrhagic Escherichia coli O145 Strains from Patients in Germany[J].Clin Microbiol,2004,42(3):954-962.
  • 5王丽丽,徐建国.脉冲场凝胶电泳技术(PFGE)在分子分型中的应用现状[J].疾病监测,2006,21(5):276-279. 被引量:126
  • 6Jang S J,Han H L,Lee S H,et al.PFGE-based epidemiological study of an outbreak of Candida tropicalis candiduria:the importance of medical waste as a reservoir of nosocomial infection[J].J Infect Dis,2005,58:263-267.
  • 7Chen K W,Lo H J,Lin Y H,et al.Comparison of four molecular typing methods to assess genetic relatedness of Candida albicans clinical isolates in Taiwan[J].J Med Microbiol,2005,54:249-258.
  • 8张文东,张应国,宋建领,张富强.猪链球菌PCR检测技术研究进展[J].动物医学进展,2006,27(6):10-14. 被引量:4
  • 9李茂林,黄健强,陈木新,娄高明.2型猪链球菌毒力因子概述[J].河南畜牧兽医,2005,26(11):9-11. 被引量:6
  • 10Hunter Susan B,Paul V,Lambert-Fair M A,et al.Establishment of a universal size standard strain for use with the pulseNet standardized pulsed-field gel electrophoresis protocols:converting the national databases to the new size standard[J].J Clin Microbiol,2005,43:1045-1050.

二级参考文献77

  • 1洪帮兴,江丽芳,胡玉山,方丹云,郭辉玉.23S rRNA基因序列分析及其在细菌鉴别诊断中的应用[J].中华微生物学和免疫学杂志,2004,24(3):241-244. 被引量:11
  • 2陈金东.脉冲场凝胶电泳技术的发展和应用现状[J].国外医学(遗传学分册),1994,17(1):13-18. 被引量:8
  • 3黄毓茂,黄引贤.2型猪链球菌的血清学鉴定[J].中国兽医学报,1995,15(1):63-65. 被引量:58
  • 4Hall JA, Goulding JS, Bean NH, et al. Epidemiologic profiling: evaluating foodborne outbreaks for which no pathogen was isolated by routine laboratoiy testing:United States, 1982-9[J]. Epidemiol Infect, 2001,127(3):381-7.
  • 5Matar GM, Koehler JE, Malcolm G, et al. Identification of Bartonella species directly in clinical speimens by PCR-restriction fragment length polymorphism analysis of a 16S rRNA gene fragment [J]. J Clin Microbiol,1999,37(12):4045-7.
  • 6Scheinert P, Krausse R, Ullmann U, et al. Molecular differention of bacteria by PCR amplification of 16S-23S rRNA spacer[J]. J Microbiol Methods, 1996,(26):103-17.
  • 7Nair S, Lin TK, Pang T, et al. Characterization of Salmonella serovars by PCR-single strand conformation polymorphism analysis[J]. J Clin Microbiol, 2002,40(7):2346-51.
  • 8Botelho BA, Bando SY,Trabulsi LR, et al. Identification of EPEC and non-EPEC serotypes in the EPEC serogroups by PCR-RFLP analysis of fliC gene [J]. J Microbiol Methods, 2003,54( 1):87-93.
  • 9Hein I, Mach RL, Famleitner AH, et al. Application of single-strain conformation polymorphism and denaturing gradient gel electrophoresis for fla sequence type of campylobacter jejune [J]. J Mierobiol Methods, 2003,(52):305-13.
  • 10Schmalenberger A, Schwieger F, Tebbe CC. Effect of primers hybridizating to different evolutionarily conserved regions of the small-subunit rRNA gene in PCR-based microbial community analyses and genetic profiling[J]. Appl Environ Microbiol, 2001(67):3557-63.

共引文献156

同被引文献109

引证文献5

二级引证文献34

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