• 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

用于检测霍乱弧菌霍乱肠毒素操纵子的聚合酶链反应。

Polymerase chain reaction for detection of the cholera enterotoxin operon of Vibrio cholerae.

作者信息

Shirai H, Nishibuchi M, Ramamurthy T, Bhattacharya S K, Pal S C, Takeda Y

机构信息

Department of Microbiology, Faculty of Medicine, Kyoto University, Japan.

出版信息

J Clin Microbiol. 1991 Nov;29(11):2517-21. doi: 10.1128/jcm.29.11.2517-2521.1991.

DOI:10.1128/jcm.29.11.2517-2521.1991
PMID:1774258
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC270365/
Abstract

We report a set of oligonucleotide primers and amplification conditions for the polymerase chain reaction to detect the ctx operon of Vibrio cholerae. The results of this assay on strains of V. cholerae and related organisms were identical with those obtained by the DNA colony hybridization test with the polynucleotide probe. The detection limit of this system was 1 pg of chromosomal DNA or broth culture containing three viable cells. The polymerase chain reaction method could directly detect the ctx operon sequences in rice-water stool samples from patients with cholera.

摘要

我们报告了一组用于聚合酶链反应检测霍乱弧菌ctx操纵子的寡核苷酸引物和扩增条件。对霍乱弧菌菌株及相关微生物进行该检测的结果,与使用多核苷酸探针进行DNA菌落杂交试验所得结果一致。该系统的检测限为1 pg染色体DNA或含有三个活细胞的肉汤培养物。聚合酶链反应方法可直接检测霍乱患者米泔水样粪便样本中的ctx操纵子序列。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e788/270365/61491421d706/jcm00047-0174-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e788/270365/dd71b36b7046/jcm00047-0173-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e788/270365/a252b389c963/jcm00047-0173-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e788/270365/61491421d706/jcm00047-0174-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e788/270365/dd71b36b7046/jcm00047-0173-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e788/270365/a252b389c963/jcm00047-0173-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e788/270365/61491421d706/jcm00047-0174-a.jpg

相似文献

1
Polymerase chain reaction for detection of the cholera enterotoxin operon of Vibrio cholerae.用于检测霍乱弧菌霍乱肠毒素操纵子的聚合酶链反应。
J Clin Microbiol. 1991 Nov;29(11):2517-21. doi: 10.1128/jcm.29.11.2517-2521.1991.
2
[Development and application of polymerase chain reaction (PCR) and DNA hybridization for detection of cholera enterotoxin-producing V. cholerae and other pathogens].[用于检测产霍乱肠毒素霍乱弧菌及其他病原体的聚合酶链反应(PCR)和DNA杂交技术的开发与应用]
Nihon Rinsho. 1992 Jul;50 Suppl:361-7.
3
Direct detection of Vibrio cholerae in stool samples.粪便样本中霍乱弧菌的直接检测。
J Clin Microbiol. 1994 May;32(5):1246-8. doi: 10.1128/jcm.32.5.1246-1248.1994.
4
[Detection of toxigenic Vibrio cholerae O1 using polymerase chain reaction for amplifying the cholera enterotoxin gene].[使用聚合酶链反应扩增霍乱肠毒素基因检测产毒霍乱弧菌O1]
Kansenshogaku Zasshi. 1990 Oct;64(10):1323-9. doi: 10.11150/kansenshogakuzasshi1970.64.1323.
5
Detection of the Vibrio cholerae heat-stable enterotoxin gene by polymerase chain reaction.用聚合酶链反应检测霍乱弧菌热稳定肠毒素基因
Mol Cell Probes. 1994 Feb;8(1):39-44. doi: 10.1006/mcpr.1994.1005.
6
[Development and testing of cholera enterotoxin gene probe for detection of toxigenic Vibrio cholerae O1].用于检测产毒霍乱弧菌O1的霍乱肠毒素基因探针的研制与测试
Kansenshogaku Zasshi. 1990 Oct;64(10):1330-6. doi: 10.11150/kansenshogakuzasshi1970.64.1330.
7
[The determination of the content of the cholera toxin gene in the composition of the DNA from Vibrio cholerae strains by means of the nested polymerase chain reaction].[利用巢式聚合酶链反应测定霍乱弧菌菌株DNA组成中霍乱毒素基因的含量]
Zh Mikrobiol Epidemiol Immunobiol. 1996 Sep-Oct(5):20-2.
8
A multiplatform real-time polymerase chain reaction detection assay for Vibrio cholerae.一种用于霍乱弧菌的多平台实时聚合酶链反应检测方法。
Diagn Microbiol Infect Dis. 2009 Nov;65(3):339-44. doi: 10.1016/j.diagmicrobio.2009.07.009. Epub 2009 Sep 2.
9
Multiplex polymerase chain reaction to detect toxigenic Vibrio cholerae and to biotype Vibrio cholerae O1.多重聚合酶链反应检测产毒霍乱弧菌及霍乱弧菌O1生物型
J Appl Bacteriol. 1995 Sep;79(3):264-73. doi: 10.1111/j.1365-2672.1995.tb03136.x.
10
[A DNA analysis of Vibrio cholerae strains by the polymerase chain reaction].[通过聚合酶链反应对霍乱弧菌菌株进行DNA分析]
Zh Mikrobiol Epidemiol Immunobiol. 1996 Jul-Aug(4):38-41.

引用本文的文献

1
Non-O1, Non-O139 Bacteremic Skin Infection with Multiple Skin Necrosis: Case Report.非O1、非O139型菌血症性皮肤感染伴多处皮肤坏死:病例报告
Trop Med Infect Dis. 2025 Apr 17;10(4):110. doi: 10.3390/tropicalmed10040110.
2
Prevalence of spp. in Seafood from German Supermarkets and Fish Markets.德国超市和鱼市海鲜中 spp. 的流行情况。
Foods. 2024 Dec 10;13(24):3987. doi: 10.3390/foods13243987.
3
Genetic and Phenotypic Virulence Potential of Non-O1/Non-O139 Isolated from German Retail Seafood.从德国零售海鲜中分离出的非O1/非O139的遗传和表型毒力潜力

本文引用的文献

1
Production of cholera-like enterotoxin by a Vibrio cholerae non-O1 strain isolated from the environment.从环境中分离出的一株非O1群霍乱弧菌产生霍乱样肠毒素。
Infect Immun. 1981 Oct;34(1):90-7. doi: 10.1128/iai.34.1.90-97.1981.
2
Molecular characterization of environmental and nontoxigenic strains of Vibrio cholerae.霍乱弧菌环境菌株和非产毒株的分子特征分析
Infect Immun. 1981 May;32(2):661-7. doi: 10.1128/iai.32.2.661-667.1981.
3
Further evaluation of the Biken test (modified Elek test) for detection of enterotoxigenic Escherichia coli producing heat-labile enterotoxin and application of the test to sampling of heat-stable enterotoxin.
Microorganisms. 2023 Nov 11;11(11):2751. doi: 10.3390/microorganisms11112751.
4
Distribution and Molecular Characteristics of Species Isolated from Aquatic Environments in China, 2020.2020年中国水生环境分离物种的分布及分子特征
Microorganisms. 2022 Oct 11;10(10):2007. doi: 10.3390/microorganisms10102007.
5
Virulence gene profiles, biofilm formation, and antimicrobial resistance of non-O1/non-O139 bacteria isolated from West Bengal, India.从印度西孟加拉邦分离出的非O1/非O139型细菌的毒力基因谱、生物膜形成及抗菌药物耐药性
Heliyon. 2018 Dec 17;4(12):e01040. doi: 10.1016/j.heliyon.2018.e01040. eCollection 2018 Dec.
6
Isolation of viable but nonculturable Vibrio cholerae O1 from environmental water samples in Kolkata, India, in a culturable state.在印度加尔各答从环境水样中分离出处于可培养状态的活的但不可培养的霍乱弧菌O1。
Microbiologyopen. 2014 Apr;3(2):239-46. doi: 10.1002/mbo3.164. Epub 2014 Feb 18.
7
Cholera toxin gene polymerase chain reaction for detection of non-culturable Vibrio cholerae O1.霍乱毒素基因聚合酶链反应检测不可培养霍乱弧菌 O1 。
World J Microbiol Biotechnol. 1994 Sep;10(5):568-71. doi: 10.1007/BF00367669.
8
Short communication: Detection of non-culturable Vibrio cholerae O139, by PCR and fluorescent antibody methods, in laboratory microcosms.短篇通讯:应用 PCR 和荧光抗体方法检测实验室微宇宙中不可培养的霍乱弧菌 O139
World J Microbiol Biotechnol. 1995 Sep;11(5):597-8. doi: 10.1007/BF00286382.
9
Detection of cholera (ctx) and zonula occludens (zot) toxin genes in Vibrio cholerae O1, O139 and non-O1 strains.检测霍乱弧菌 O1、O139 及非 O1 菌株中的霍乱毒素 (ctx) 和紧密连接蛋白 (zonula occludens, zot) 毒素基因。
World J Microbiol Biotechnol. 1995 Sep;11(5):572-7. doi: 10.1007/BF00286376.
10
Real-time PCR threshold cycle cutoffs help to identify agents causing acute childhood diarrhea in Zanzibar.实时聚合酶链反应阈值循环截断值有助于识别桑给巴尔岛引起儿童急性腹泻的病原体。
J Clin Microbiol. 2014 Mar;52(3):916-23. doi: 10.1128/JCM.02697-13. Epub 2014 Jan 8.
用于检测产热不稳定肠毒素的产肠毒素性大肠杆菌的比肯试验(改良埃莱克试验)的进一步评估以及该试验在热稳定肠毒素采样中的应用。
J Clin Microbiol. 1982 Jul;16(1):60-2. doi: 10.1128/jcm.16.1.60-62.1982.
4
Identification of enterotoxigenic Escherichia coli by colony hybridization using three enterotoxin gene probes.使用三种肠毒素基因探针通过菌落杂交鉴定产肠毒素大肠杆菌
J Infect Dis. 1982 Jun;145(6):863-9. doi: 10.1093/infdis/145.6.863.
5
Cholera toxin genes: nucleotide sequence, deletion analysis and vaccine development.霍乱毒素基因:核苷酸序列、缺失分析与疫苗研发
Nature. 1983;306(5943):551-7. doi: 10.1038/306551a0.
6
Primary structure of heat-labile enterotoxin produced by Escherichia coli pathogenic for humans.由对人类致病的大肠杆菌产生的不耐热肠毒素的一级结构。
J Biol Chem. 1984 Apr 25;259(8):5037-44.
7
Purification and some properties of a non-o1 Vibrio cholerae enterotoxin that is identical to cholera enterotoxin.一种与霍乱肠毒素相同的非O1群霍乱弧菌肠毒素的纯化及其某些特性
Infect Immun. 1983 Mar;39(3):1128-35. doi: 10.1128/iai.39.3.1128-1135.1983.
8
Detection of the thermostable direct hemolysin gene and related DNA sequences in Vibrio parahaemolyticus and other vibrio species by the DNA colony hybridization test.通过DNA菌落杂交试验检测副溶血性弧菌及其他弧菌属中的耐热直接溶血素基因和相关DNA序列。
Infect Immun. 1985 Sep;49(3):481-6. doi: 10.1128/iai.49.3.481-486.1985.
9
Detection with synthetic oligonucleotide probes of nucleotide sequence variations in the genes encoding enterotoxins of Escherichia coli.用合成寡核苷酸探针检测大肠杆菌肠毒素编码基因中的核苷酸序列变异。
J Clin Microbiol. 1989 Oct;27(10):2272-6. doi: 10.1128/jcm.27.10.2272-2276.1989.
10
Detection of enterotoxigenic Escherichia coli after polymerase chain reaction amplification with a thermostable DNA polymerase.使用耐热DNA聚合酶进行聚合酶链反应扩增后检测产肠毒素大肠杆菌
J Clin Microbiol. 1989 Feb;27(2):261-5. doi: 10.1128/jcm.27.2.261-265.1989.