• 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

相似文献

1
Comparison of restriction enzyme analysis, arbitrarily primed PCR, and protein profile analysis typing for epidemiologic investigation of an ongoing Clostridium difficile outbreak.用于艰难梭菌持续爆发流行病学调查的限制性内切酶分析、随机引物PCR和蛋白质谱分析分型的比较
J Clin Microbiol. 1998 Oct;36(10):2957-63. doi: 10.1128/JCM.36.10.2957-2963.1998.
2
Multicenter typing comparison of sporadic and outbreak Clostridium difficile isolates from geographically diverse hospitals.来自不同地理位置医院的散发性和暴发艰难梭菌分离株的多中心分型比较
J Infect Dis. 1997 Nov;176(5):1233-8. doi: 10.1086/514117.
3
Molecular epidemiology of endemic Clostridium difficile infection and the significance of subtypes of the United Kingdom epidemic strain (PCR ribotype 1).地方性艰难梭菌感染的分子流行病学及英国流行菌株(PCR核糖体分型1)亚型的意义
J Clin Microbiol. 2005 Jun;43(6):2685-96. doi: 10.1128/JCM.43.6.2685-2696.2005.
4
Analysis of Clostridium difficile isolates from nosocomial outbreaks at three hospitals in diverse areas of Japan.对来自日本不同地区三家医院医院感染暴发中艰难梭菌分离株的分析。
J Clin Microbiol. 2001 Apr;39(4):1391-5. doi: 10.1128/JCM.39.4.1391-1395.2001.
5
Arbitrary primed PCR rules out Clostridium difficile cross-infection among patients in a haematology unit.
J Hosp Infect. 1997 Feb;35(2):107-15. doi: 10.1016/s0195-6701(97)90099-2.
6
Isolation of various genotypes of Clostridium difficile from patients and the environment in an oncology ward.从肿瘤病房的患者和环境中分离出不同基因型的艰难梭菌。
Clin Infect Dis. 1997 May;24(5):889-93. doi: 10.1093/clinids/24.5.889.
7
PCR ribotyping and arbitrarily primed PCR for typing strains of Clostridium difficile from a Polish maternity hospital.用于对波兰一家妇产医院艰难梭菌菌株进行分型的聚合酶链反应核糖体分型和任意引物聚合酶链反应
J Clin Microbiol. 1995 Aug;33(8):2016-21. doi: 10.1128/jcm.33.8.2016-2021.1995.
8
Wide diversity of Clostridium difficile types at a tertiary referral hospital.
J Infect Dis. 1994 Sep;170(3):615-21. doi: 10.1093/infdis/170.3.615.
9
Comparison of seven techniques for typing international epidemic strains of Clostridium difficile: restriction endonuclease analysis, pulsed-field gel electrophoresis, PCR-ribotyping, multilocus sequence typing, multilocus variable-number tandem-repeat analysis, amplified fragment length polymorphism, and surface layer protein A gene sequence typing.七种艰难梭菌国际流行菌株分型技术的比较:限制性内切酶分析、脉冲场凝胶电泳、PCR核糖体分型、多位点序列分型、多位点可变数目串联重复分析、扩增片段长度多态性以及表层蛋白A基因序列分型。
J Clin Microbiol. 2008 Feb;46(2):431-7. doi: 10.1128/JCM.01484-07. Epub 2007 Nov 26.
10
Multilocus variable-number tandem-repeat analysis for investigation of Clostridium difficile transmission in Hospitals.多位点可变数目串联重复序列分析用于医院艰难梭菌传播的调查。
J Clin Microbiol. 2006 Jul;44(7):2558-66. doi: 10.1128/JCM.02364-05.

引用本文的文献

1
Update on Commonly Used Molecular Typing Methods for .关于……常用分子分型方法的最新进展 。 你提供的原文似乎不完整,最后的“for.”后面缺少具体内容。
Microorganisms. 2023 Jul 5;11(7):1752. doi: 10.3390/microorganisms11071752.
2
Rapid molecular characterization of Clostridium difficile and assessment of populations of C. difficile in stool specimens.艰难梭菌的快速分子特征分析及粪便标本中艰难梭菌菌群的评估。
J Clin Microbiol. 2009 Jul;47(7):2142-8. doi: 10.1128/JCM.02498-08. Epub 2009 Apr 29.
3
Comparison of the value of pulsed-field gel electrophoresis, random amplified polymorphic DNA and amplified rDNA restriction analysis for subtyping Taylorella equigenitalis.脉冲场凝胶电泳、随机扩增多态性DNA和扩增rDNA限制性分析用于马生殖道泰勒菌分型的价值比较
Vet Res Commun. 2001 May;25(4):261-9. doi: 10.1023/a:1010674524428.

本文引用的文献

1
Multicenter typing comparison of sporadic and outbreak Clostridium difficile isolates from geographically diverse hospitals.来自不同地理位置医院的散发性和暴发艰难梭菌分离株的多中心分型比较
J Infect Dis. 1997 Nov;176(5):1233-8. doi: 10.1086/514117.
2
Preliminary findings of the international typing study on Clostridium difficile. International Clostridium Difficile Study Group.
Clin Infect Dis. 1997 Sep;25 Suppl 2:S199-201. doi: 10.1086/516190.
3
Genotyping of outbreak-related and sporadic isolates of Clostridium difficile belonging to serogroup C.属于C血清型的艰难梭菌暴发相关及散发病例分离株的基因分型
J Clin Microbiol. 1996 Dec;34(12):3049-55. doi: 10.1128/jcm.34.12.3049-3055.1996.
4
Comparison of PCR-based approaches to molecular epidemiologic analysis of Clostridium difficile.基于聚合酶链反应的艰难梭菌分子流行病学分析方法比较
J Clin Microbiol. 1996 May;34(5):1153-7. doi: 10.1128/jcm.34.5.1153-1157.1996.
5
Comparison of arbitrarily primed PCR with restriction endonuclease and immunoblot analyses for typing Clostridium difficile isolates.任意引物PCR与限制性内切酶及免疫印迹分析用于艰难梭菌分离株分型的比较
J Clin Microbiol. 1995 Dec;33(12):3169-73. doi: 10.1128/jcm.33.12.3169-3173.1995.
6
Clinical and molecular epidemiology of sporadic and clustered cases of nosocomial Clostridium difficile diarrhea.散发性和聚集性医院内艰难梭菌腹泻病例的临床和分子流行病学
Am J Med. 1996 Jan;100(1):32-40. doi: 10.1016/s0002-9343(96)90008-x.
7
Molecular epidemiology: application of contemporary techniques to the typing of microorganisms.分子流行病学:当代技术在微生物分型中的应用。
Clin Infect Dis. 1993 Aug;17(2):153-62; quiz 163-4. doi: 10.1093/clinids/17.2.153.
8
Development of a rapid and efficient restriction endonuclease analysis typing system for Clostridium difficile and correlation with other typing systems.艰难梭菌快速高效限制性内切酶分析分型系统的开发及其与其他分型系统的相关性。
J Clin Microbiol. 1993 Jul;31(7):1870-5. doi: 10.1128/jcm.31.7.1870-1875.1993.
9
Epidemic Clostridium difficile-associated diarrhea: role of second- and third-generation cephalosporins.
Infect Control Hosp Epidemiol. 1994 Feb;15(2):88-94. doi: 10.1086/646867.
10
Comparison of typing methods for Clostridium difficile isolates.艰难梭菌分离株分型方法的比较
J Clin Microbiol. 1993 Aug;31(8):2208-11. doi: 10.1128/jcm.31.8.2208-2211.1993.

用于艰难梭菌持续爆发流行病学调查的限制性内切酶分析、随机引物PCR和蛋白质谱分析分型的比较

Comparison of restriction enzyme analysis, arbitrarily primed PCR, and protein profile analysis typing for epidemiologic investigation of an ongoing Clostridium difficile outbreak.

作者信息

Rafferty M E, Baltch A L, Smith R P, Bopp L H, Rheal C, Tenover F C, Killgore G E, Lyerly D M, Wilkins T D, Schoonmaker D J, Hannett G E, Shayegani M

机构信息

Stratton Veterans Affairs Medical Center and Albany Medical College, New York State Department of Health, Albany, New York, USA.

出版信息

J Clin Microbiol. 1998 Oct;36(10):2957-63. doi: 10.1128/JCM.36.10.2957-2963.1998.

DOI:10.1128/JCM.36.10.2957-2963.1998
PMID:9738050
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC105094/
Abstract

During an outbreak of diarrhea in a general hospital in 1992, 166 Clostridium difficile isolates from 102 patients were typed by restriction enzyme analysis (REA), arbitrarily primed PCR (AP-PCR), and protein profile analysis (PP) techniques. A total of 18 types and 5 subtypes were identified by REA, 32 types were identified by AP-PCR, and 9 types were identified by PP. Analysis of the data indicated the presence of a predominant strain among 76, 75, and 84% of the isolates by REA, AP-PCR, and PP, respectively. Subsequently, 45 C. difficile isolates which had been collected in 1990 from 33 patients in the same hospital following a significant increase in the number of cases of diarrhea caused by C. difficile were studied by REA, AP-PCR, and PP typing techniques. Thirteen types and one subtype were identified by REA, 12 types were identified by AP-PCR, and 5 types were identified by PP. As with the isolates from 1992, a dominant strain was identified. This strain was represented by 53, 64, and 70% of the total number of isolates when the strains were typed by REA, AP-PCR, and PP, respectively. Every isolate (210 of 211) from both 1990 and 1992 that was available for typing was typeable by all three methods. Furthermore, the same dominant strain was identified in both 1990 and 1992 by each method. This study demonstrates that each of the three typing methods can be useful in epidemiologic investigations of C. difficile outbreaks and that one strain can be dominant in an institution over a number of years.

摘要

1992年,一家综合医院爆发腹泻疫情,采用限制性内切酶分析(REA)、随机引物PCR(AP-PCR)和蛋白质谱分析(PP)技术,对102例患者的166株艰难梭菌分离株进行了分型。REA共鉴定出18种类型和5种亚型,AP-PCR鉴定出32种类型,PP鉴定出9种类型。数据分析表明,REA、AP-PCR和PP分别在76%、75%和84%的分离株中存在优势菌株。随后,对1990年从同一家医院33例患者中收集的45株艰难梭菌分离株进行了研究,当时艰难梭菌引起的腹泻病例数显著增加,采用REA、AP-PCR和PP分型技术。REA鉴定出13种类型和1种亚型,AP-PCR鉴定出12种类型,PP鉴定出5种类型。与1992年的分离株一样,鉴定出了优势菌株。当分别用REA、AP-PCR和PP对菌株进行分型时,该菌株分别占分离株总数的53%、64%和70%。1990年和1992年所有可用于分型的分离株(211株中的210株)均可用这三种方法进行分型。此外,每种方法在1990年和1992年都鉴定出了相同的优势菌株。本研究表明,这三种分型方法均可用于艰难梭菌疫情的流行病学调查,并且一种菌株在一个机构中可能多年占主导地位。