Detection of verotoxin-producing Escherichia coli in stool specimens by the polymerase chain reaction

FTH Chan , N Stewart , F Diaz-Mitoma , PN McLaine
{"title":"Detection of verotoxin-producing Escherichia coli in stool specimens by the polymerase chain reaction","authors":"FTH Chan ,&nbsp;N Stewart ,&nbsp;F Diaz-Mitoma ,&nbsp;PN McLaine","doi":"10.1016/0888-0786(94)90030-2","DOIUrl":null,"url":null,"abstract":"<div><p>In this retrospective study a total of 404 stools kept at −70°C were tested for the presence of verotoxin-producing <em>Escherichia coli</em> (VTEC) by the polymerase chain reaction (PCR). Thirteen positive samples from 11 patients were identified by PCR which correlated with previous isolation of <em>E. coli</em> O157:H7. There was no failure to detect VTEC by PCR but PCR did not identify further VTEC isolates. We concluded that (a) the occurrence of VTEC other than serotype O157:H7 is rare in our demographic area, (b) PCR is effective in the identification of <em>E. coli</em> O157:H7, and (c) PCR has the additional advantage over conventional culture methods of identifying VTEC, including sorbitol-fermenting serotypes, which might have been detected if we had extended our sample size.</p></div>","PeriodicalId":101161,"journal":{"name":"Serodiagnosis and Immunotherapy in Infectious Disease","volume":"6 4","pages":"Pages 185-188"},"PeriodicalIF":0.0000,"publicationDate":"1994-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0888-0786(94)90030-2","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Serodiagnosis and Immunotherapy in Infectious Disease","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0888078694900302","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

In this retrospective study a total of 404 stools kept at −70°C were tested for the presence of verotoxin-producing Escherichia coli (VTEC) by the polymerase chain reaction (PCR). Thirteen positive samples from 11 patients were identified by PCR which correlated with previous isolation of E. coli O157:H7. There was no failure to detect VTEC by PCR but PCR did not identify further VTEC isolates. We concluded that (a) the occurrence of VTEC other than serotype O157:H7 is rare in our demographic area, (b) PCR is effective in the identification of E. coli O157:H7, and (c) PCR has the additional advantage over conventional culture methods of identifying VTEC, including sorbitol-fermenting serotypes, which might have been detected if we had extended our sample size.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
聚合酶链反应检测粪便标本中产维罗毒素大肠杆菌
在这项回顾性研究中,用聚合酶链反应(PCR)检测了404份保存在- 70°C的粪便中是否存在产维罗毒素的大肠杆菌(VTEC)。对11例患者的13份阳性样本进行PCR鉴定,结果与先前分离到的大肠杆菌O157:H7相关。PCR没有检测到VTEC的失败,但PCR没有发现进一步的VTEC分离株。我们得出结论:(a)除O157:H7血清型外的VTEC在我们的人口统计区域很少发生,(b) PCR在鉴定大肠杆菌O157:H7中是有效的,(c) PCR在鉴定VTEC方面比传统培养方法有额外的优势,包括山梨醇发酵血清型,如果我们扩大样本量,可能会检测到VTEC。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Subject index Volume contents Author index The value of ELISA vs. negative Coombs findings in the serodiagnosis of human brucellosis Detection of toxoplasma-specific antibody in human saliva using conventional assays
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1