期刊文献+

聚合酶链反应扩增STY3671基因鉴别伤寒与甲型副伤寒沙门菌 被引量:2

Identification of Salmonella typhi and Salmonella paratyphi A by PCR amplification of gene STY3671
原文传递
导出
摘要 目的评价伤寒沙门菌基因STY3671用于特异性检测该血清型沙门菌的可能性。方法根据伤寒沙门菌与甲型副伤寒沙门菌外膜蛋白质组比较得到的伤寒沙门菌特异性蛋白点编码基因STY3671的序列设计引物,提取伤寒沙门菌、甲型副伤寒沙门菌以及其他非伤寒沙门菌血清型菌株的基因组DNA进行PCR检测,对引物特异性和灵敏性进行分析。结果检测的184株伤寒沙门菌均得到807 bp长度片段,部分菌株扩增产物测序结果与伤寒沙门菌标准株CT-18一致。146株甲型副伤寒沙门菌以及其余163株其他血清型沙门菌均未扩增出该片段。结论 STY3671基因能够作为特异性检测伤寒沙门菌的靶标,能够区别于甲型副伤寒沙门菌及其他常见非伤寒沙门菌血清型,在发热患者的伤寒沙门菌感染诊断、尤其使用血液标本检测中具有良好的潜在价值。 Objective To evaluate the feasibility of using gene STY3671 in detection of Samonella typhi.MethodsProteomics comparison between outer membrane proteins of S.typhi and S.paratyphi A was conducted,one of the specific dots was identified,and primers were designed according to its coding sequence,PCR test was performed by using epidemic strains of Salmonella,then the sensitivity and specificity of the assay were evaluated.Results A 807 bp PCR fragment was successfully amplified from all 184 strains of S.typhi,random sequencing of the fragments showed coincidence with gene STY3671 in strain CT-18.No fragment was amplified from any S.paratyphi A and other Salmonella strains.Conclusion STY3671 is a specific target to distinguish S.typhi from S.paratyohi A and other Salmonella,this assay has high sensitivity and specificity and might be used in diagnosis of typhoid fever.
出处 《疾病监测》 CAS 2012年第3期181-183,199,共4页 Disease Surveillance
基金 国家科技重大专项课题(No.2008ZX10004-013)~~
关键词 伤寒沙门菌 检测 聚合酶链反应 Samonella typhi test polymerase chain reaction
  • 相关文献

参考文献2

二级参考文献10

  • 1闫梅英,梁未丽,李伟,阚飙.1995-2004年全国伤寒副伤寒的流行分析[J].疾病监测,2005,20(8):401-403. 被引量:104
  • 2Ansong C,Yoon H,Norbeck AD,et al.Proteomics analysis of the causative agent of typhoid fever[J].J Proteomics Res,2008,7(2):546-557. 被引量:1
  • 33 Jeannin P,Magistrelli G,Goetsch L,et al.Outer membrane protein A(OmpA):a new pathogen-associated molecular pattern that interacts with antigen presenting cells-impact on vaccine strategies[J].Vaccine,2002,20(Suppl 4):A23-27. 被引量:1
  • 4Mittal R,Prasadarao N V.Outer membrane protein A expression in Escherichia coli K1 is required to prevent the maturation of myeloid dendritic cells and the induction of IL-10 and TGF-beta[J].J Immunol,2008,181(4):2672-2682. 被引量:1
  • 5Mizuno T,Mizushima S.signal transduction and gene regulation through the phosphorylation of two regulatory components:the molecular basis for the osmotic regulation of the porin genes[J].Mol Microbiol,1990,4(7):1077-1082. 被引量:1
  • 6Sood S, Kapil A, Dash N, et al. Paratyphoid Fever in India:An Emerging Problem [J]. Emerg Infect Dis. 1999, 5(3):483-484 被引量:1
  • 7Goh YL, Puthucheary SD, Chaudhry R, et al. Genetic diversity of Salmonella enterica serovar Paratyphi A from different geographical regions in Asia[J]. J Appl Microbiol, 2002, 92(6): 1167 被引量:1
  • 8Thong KL, Nair S, Chaudhry R, et al. Molecular analysis of Salmonella paratyphi A from an outbreak in New Delhi, India[J].Emerg Infect Dis. 1998,4(3):507-508. 被引量:1
  • 9陶沁,何平,谢阳,潘家秀.贵州省伤寒、副伤寒流行回顾性分析[J].中华流行病学杂志,2003,24(8):746-746. 被引量:36
  • 10林玫,唐振柱,董柏青,曾竣,王鸣柳,李翠云,龚健,梁大斌.1993~2002年广西伤寒、副伤寒流行特征及防治对策分析[J].华南预防医学,2003,29(4):10-12. 被引量:51

共引文献103

同被引文献23

  • 1Crump J A, Luby S P, Mintz E D. The global burden of typhiod fever [ J ]. Bull World Health Organ, 2004, 82 (5) :346-353. 被引量:1
  • 2Massi M N, Shirakawa T, Gotoh A, et al. Rapid diagnosis of typhoid fever by PCR assay using one pair of primers from flagellin gene of Salmonella typhi[ J]. J Infect Chemother, 2003, 9(3) :233-237. 被引量:1
  • 3Song J H, Cho H, Park M Y, et al. Detection of Salmonella typhi in the blood of patients with typhoid fever by polymerase chain reaction [ J ]. J Clin Microbiol, 1993,31 (6) : 1439-1443. 被引量:1
  • 4Ngan G J, Ng LM, Lin R T, multiplex PCR for the detection et al. Development of a novel and differentiation of Salmonella enterica serovars Typhi and Paratyphi A [ J ]. Res Microbiol, 2010, 161(4) : 243-248. 被引量:1
  • 5Hirose K, Itoh K, Nakajima H, et al. Selective amplification of tyv (rfbE) , prt (ribS) , viaB, and fliC genes by multiplex PCR for identification of Salmonella enterica serovars Typhi and Paratyphi A [ J ]. J Clin Microbiol, 2002, 40 ( 2 ) :633-636. 被引量:1
  • 6Nga T V, Karkey A, Dongol S, et al. The sensitivity of real-time PCR amplification targeting invasive Salmonella serovars in biological specimens[J]. BMC Infect Dis, 2010, 10(5 ) : 125- 133. 被引量:1
  • 7Nagarajan A G, Karnam G, Lahir A, et al. Reliable means of diagnosis and serovar determination of blood-borne Salmonella strains : quick PCR amplification of unique genomic loci by novel primer sets [ J ]. J Clin Microbiol, 2009, 47 ( 8 ) : 2435-2441. 被引量:1
  • 8Francois P, Tangomo M, Hibbs J, et al. Robustness of a loop- mediated isothermalamplication reaction for diagnostic applications[ J]. FEMS Immunol Med Microbiol, 2011, 62 ( 1 ) : 41-48. 被引量:1
  • 9Lau Y L, Meganathan P, Sonaimuthu P, et al. Specific, sensitive, and rapid diagnosis of active toxoplasmosis by a loop- mediated isothermal amplification method using blood samples from patients [J]. J Clin Microbiol, 2010, 48(10) : 3698-3702. 被引量:1
  • 10Niu J H, Jian H, Guo Q X, et al. Evaluation of loop-mediated isothermal amplification (LAMP) assays based on 5S rDNA-IGS2 regions for detecting Meloidogyne enterolobii [ J ]. Plant Pathol, 2012, 61(4) :809-819. 被引量:1

引证文献2

二级引证文献8

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