期刊文献+

五种血清型柯萨奇病毒的实时荧光RT-PCR检测方法研究 被引量:1

Research on Detection of Five Serotypes of Coxsackie Viruses with Real-Time RT-PCR
下载PDF
导出
摘要 在柯萨奇病毒基因组VP1区设计引物和探针,分别建立了特异性检测5种血清型(A9、A16、B2、B3和B5型)柯萨奇病毒(Coxsackievirus)基于MGB探针的实时荧光RT-PCR方法。通过构建的分别适于5种血清型病毒检测的质粒标准分子对建立的检测体系进行了灵敏度分析,确定5种血清型柯萨奇病毒检测体系的检测下限均为2拷贝质粒标准分子DNA。 Based on the VP1 region of Coxsackivirus genome, primer and probe sets have been designed to detect five serotypes of Coxsackieviruses (A9, A16, B2, B3 and B5) separately by real - time RT - PCR. Plasmid standard molecules suitable for coxsaekieviruse A9, A16, B2, B3 and B5 detection were constructed respectively. Limits of detection (LODs) of the developed detection systems for five serotypes of Coxsackieviruse were all 2 copies of plasmid standard molecule DNA.
出处 《检验检疫学刊》 2010年第4期1-5,11,共6页 Journal of Inspection and Quarantine
基金 上海技术标准专项项目(07DZ05026) 国家质检总局科研项目(2007B150) 科技部世博科技专项(2009BAK43B31) 上海市科委创新平台服务项目项目(10DZ2294102)
关键词 柯萨奇病毒 实时荧光RT-PCR 质粒标准分子 TAQMAN-MGB探针 Coxsackievirus Plasmid Standard Molecule Real - Time RT - PCR Taqman - MGB Probe
  • 相关文献

参考文献12

  • 1史雯,卢亦愚,严菊英,陈寅,李珏.浙江省2006年柯萨奇B3病毒VP1基因分析[J].中国卫生检验杂志,2008,18(4):599-601. 被引量:5
  • 2潘良文,张舒亚,李晓虹,严罗美,李树清,王巧全.贝类产品中诺沃克病毒的实时荧光RT-PCR检测方法研究[J].检验检疫科学,2004,14(5):1-3. 被引量:13
  • 3施弦,刘克红.一起柯萨奇病毒爆发流行的诊治分析[J].浙江实用医学,2004,9(2):126-127. 被引量:1
  • 4陈曙霞,谢龙山,梅尚文,钱富荣,陈美芳.柯萨奇病毒BRNA与中和抗体检测在病毒性心肌炎诊断中的意义[J].中华检验医学杂志,2003,26(3):166-168. 被引量:4
  • 5www.ggwsj.gov.cn/UploadFile/200805/12/1036166845.doc . 2008
  • 6Tana E L,Chowa VTK,Quakc S H.Development of multiplexreal-time hybridization probe reverse transcriptase polymerasechain reaction for specific detection and differentiation of Entero-virus 71 and Coxsackievirus A16. Diagnostic Microbiology andInfectious Disease . 2008
  • 7Justin WAB,Patrick S O,et a1.Serotype-specific detection ofCoxsackievirus A16 in clinical specimens by reverse transcription-nested PCR. Journal of Clinical Microbiology . 2001
  • 8Kageyama T,Kojima S,Shinohara M,et al.Broadly reactive and highly sensitive assay for Norwalk-like viruses based on real-time quantitative reverse transcription-PCR. Journal of Clinical Microbiology . 2003
  • 9Kojima S,Kageyama T,Fukush i S,et al.Genogroup-specific PCRprim ers for detection of Norwalk-like virus. J V irolM eth . 2002
  • 10Kutyavin IV,Afonina IA,Mills A,et al.3-minor groove binder-DNA probes increase sequence specificity at PCR extension temperatures. Nucleic Acids Research . 2000

二级参考文献16

共引文献19

同被引文献8

引证文献1

二级引证文献2

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