• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

通过脉冲场凝胶电泳和PCR核糖体分型对艰难梭菌菌株进行分子分型及长期比较

Molecular typing and long-term comparison of clostridium difficile strains by pulsed-field gel electrophoresis and PCR-ribotyping.

作者信息

Spigaglia P, Cardines R, Rossi S, Menozzi M G, Mastrantonio P

机构信息

Department of Bacteriology and Medical Mycology, Istituto Superiore di Sanità, Viale Regina Elena 299, 00161 Rome and *Institute of Microbiology, Faculty of Medicine and Surgery, University of Parma, Viale Gramsci 14, 43100 Parma, Italy.

出版信息

J Med Microbiol. 2001 May;50(5):407-414. doi: 10.1099/0022-1317-50-5-407.

DOI:10.1099/0022-1317-50-5-407
PMID:11339247
Abstract

Thirty-two related and 68 unrelated isolates of Clostridium difficile, isolated in different Italian hospitals since 1987, were analysed by PFGE and PCR-ribotyping to investigate their genetic relatedness. The isolates were classified into 28 groups by PFGE and 20 ribotypes by PCR-ribotyping. A single clone of C. difficile was recognised as the cause of three geographically and chronologically distant outbreaks. The correlation between PFGE and PCR-ribotyping results was good, with agreement for 77 (84%) of the 92 isolates typed by both methods. However, among sporadic isolates the discriminatory power of PFGE was more evident. Eight isolates that were untypable by PFGE could be analysed by PCR-ribotyping. The dendrograms generated showed that the genetic relatedness of the C. difficile isolates obtained by both techniques was comparable. The majority of the isolates in recent years appeared to be genetically unrelated to isolates from past infections. However, two clonal groups identified in all time periods had a common origin and this seems to indicate that they share some advantageous biological characteristics. The constant monitoring of C. difficile epidemiology will allow acquisition of further important data on this nosocomial pathogen.

摘要

自1987年以来,从意大利不同医院分离出32株相关艰难梭菌菌株和68株不相关艰难梭菌菌株,采用脉冲场凝胶电泳(PFGE)和PCR核糖体分型法对其进行分析,以研究它们的遗传相关性。通过PFGE将这些菌株分为28组,通过PCR核糖体分型法分为20个核糖体分型。单一的艰难梭菌克隆被确认为三起在地理和时间上相隔较远的暴发的病因。PFGE和PCR核糖体分型结果之间的相关性良好,两种方法分型的92株菌株中有77株(84%)结果一致。然而,在散发菌株中,PFGE的鉴别力更为明显。8株无法用PFGE分型的菌株可用PCR核糖体分型法进行分析。生成的树形图表明,两种技术获得的艰难梭菌菌株的遗传相关性具有可比性。近年来的大多数菌株在基因上似乎与过去感染的菌株无关。然而,在所有时间段鉴定出的两个克隆组有共同起源,这似乎表明它们具有一些有利的生物学特性。对艰难梭菌流行病学的持续监测将有助于获取有关这种医院病原体的更多重要数据。

相似文献

1
Molecular typing and long-term comparison of clostridium difficile strains by pulsed-field gel electrophoresis and PCR-ribotyping.通过脉冲场凝胶电泳和PCR核糖体分型对艰难梭菌菌株进行分子分型及长期比较
J Med Microbiol. 2001 May;50(5):407-414. doi: 10.1099/0022-1317-50-5-407.
2
Comparison of PCR-ribotyping, arbitrarily primed PCR, and pulsed-field gel electrophoresis for typing Clostridium difficile.用于艰难梭菌分型的聚合酶链反应核糖体分型、任意引物聚合酶链反应和脉冲场凝胶电泳的比较
J Clin Microbiol. 2000 Jul;38(7):2484-7. doi: 10.1128/JCM.38.7.2484-2487.2000.
3
Comparison of repetitive extragenic palindromic sequence-based PCR with PCR ribotyping and pulsed-field gel electrophoresis in studying the clonality of Clostridium difficile.重复外回文序列基聚合酶链反应与聚合酶链反应核糖体分型和脉冲场凝胶电泳在研究艰难梭菌克隆性中的比较。
Clin Microbiol Infect. 2011 Feb;17(2):166-75. doi: 10.1111/j.1469-0691.2010.03221.x.
4
Direct PCR-Ribotyping of Clostridium difficile.艰难梭菌的直接PCR核糖体分型
Methods Mol Biol. 2016;1476:15-21. doi: 10.1007/978-1-4939-6361-4_2.
5
Reprint of New opportunities for improved ribotyping of C. difficile clinical isolates by exploring their genomes.重新印刷版:通过探索艰难梭菌临床分离株的基因组,为改进核糖体分型提供新机会。
J Microbiol Methods. 2013 Dec;95(3):425-40. doi: 10.1016/j.mimet.2013.09.009. Epub 2013 Sep 16.
6
Comparison of ribotyping, pulsed-field gel electrophoresis and random amplified polymorphic DNA for typing Clostridium difficile strains.用于艰难梭菌菌株分型的核糖体分型、脉冲场凝胶电泳和随机扩增多态性DNA的比较
FEMS Microbiol Lett. 1994 Sep 15;122(1-2):61-8. doi: 10.1111/j.1574-6968.1994.tb07144.x.
7
Development of a new PCR-ribotyping method for Clostridium difficile based on ribosomal RNA gene sequencing.基于核糖体RNA基因测序开发一种用于艰难梭菌的新型PCR核糖体分型方法。
FEMS Microbiol Lett. 1999 Jun 15;175(2):261-6. doi: 10.1111/j.1574-6968.1999.tb13629.x.
8
Use of different molecular typing methods for the study of heterogeneity within Clostridium difficile toxinotypes V and III.应用不同的分子分型方法研究艰难梭菌毒素型 V 和 III 的异质性。
J Med Microbiol. 2011 Aug;60(Pt 8):1101-1107. doi: 10.1099/jmm.0.031054-0. Epub 2011 Mar 24.
9
A modified pulsed-field gel electrophoresis (PFGE) protocol for subtyping previously non-PFGE typeable isolates of Clostridium difficile polymerase chain reaction ribotype 001.一种改良的脉冲场凝胶电泳(PFGE)方案,用于对艰难梭菌聚合酶链反应核糖体分型001的先前不可用PFGE分型的分离株进行分型。
J Hosp Infect. 2005 Nov;61(3):231-6. doi: 10.1016/j.jhin.2005.01.017. Epub 2005 Jul 5.
10
Molecular typing methods for Clostridium difficile: pulsed-field gel electrophoresis and PCR ribotyping.艰难梭菌的分子分型方法:脉冲场凝胶电泳和聚合酶链反应核糖体分型
Methods Mol Biol. 2010;646:55-65. doi: 10.1007/978-1-60327-365-7_4.

引用本文的文献

1
The A, B, BI, and Cs of Clostridium difficile.艰难梭菌的A、B、BI和C类因素
Clin Infect Dis. 2009 Oct 15;49(8):1148-52. doi: 10.1086/605639.
2
Typing Clostridium difficile strains based on tandem repeat sequences.基于串联重复序列对艰难梭菌菌株进行分型。
BMC Microbiol. 2009 Jan 8;9:6. doi: 10.1186/1471-2180-9-6.
3
Newer diagnostic tests for bacterial diseases.细菌性疾病的新型诊断测试。
Indian J Pediatr. 2007 Jul;74(7):673-7. doi: 10.1007/s12098-007-0119-6.
4
Molecular analysis of Clostridium difficile at a university teaching hospital in Japan: a shift in the predominant type over a five-year period.日本一家大学教学医院艰难梭菌的分子分析:五年间优势菌株类型的转变
Eur J Clin Microbiol Infect Dis. 2007 Oct;26(10):695-703. doi: 10.1007/s10096-007-0355-8.
5
Multilocus sequence typing analysis of human and animal Clostridium difficile isolates of various toxigenic types.对不同产毒类型的人源和动物源艰难梭菌分离株进行多位点序列分型分析。
J Clin Microbiol. 2004 Jun;42(6):2609-17. doi: 10.1128/JCM.42.6.2609-2617.2004.
6
Evaluation of repetitive element sequence-based PCR as a molecular typing method for Clostridium difficile.基于重复元件序列的聚合酶链反应作为艰难梭菌分子分型方法的评估
J Clin Microbiol. 2003 Jun;41(6):2454-7. doi: 10.1128/JCM.41.6.2454-2457.2003.
7
Molecular analysis of the pathogenicity locus and polymorphism in the putative negative regulator of toxin production (TcdC) among Clostridium difficile clinical isolates.艰难梭菌临床分离株中毒素产生假定负调控因子(TcdC)的致病性位点及多态性的分子分析
J Clin Microbiol. 2002 Sep;40(9):3470-5. doi: 10.1128/JCM.40.9.3470-3475.2002.