• 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

使用聚合酶链式反应(PCR)方法评估用于检测……的不同引物

Evaluation of Different Primers for Detection of by Using PCR Method.

作者信息

Moulana Zahra, Roushan Mohammad Reza Hasanjani, Marashi Seyed Mahmoud Amin

机构信息

Ph.D. in Biomedical Sciences, Infectious Diseases and Tropical Medicine Research Center, Babol University of Medical Sciences, Babol, Iran.

Professor of Infectious Diseases, Infectious Diseases and Tropical Medicine Research Center, Babol University of Medical Sciences, Babol, Iran.

出版信息

Electron Physician. 2016 Nov 25;8(11):3222-3227. doi: 10.19082/3222. eCollection 2016 Nov.

DOI:10.19082/3222
PMID:28070255
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5217814/
Abstract

INTRODUCTION

Brucellosis is a worldwide zoonosis and a significant cause of loss of health in humans and animals. Traditionally, classic diagnosis is carried out by isolation of , which is time-consuming, technically challenging and potentially dangerous. The aim of this study was to expand a molecular test that would be used for the develop detection of in a single reaction with high sensitivity and specificity, by targeting IS711element.

METHODS

This study was carried out from 2015 to 2016 at the Ayatolla Rohani hospital in Babol, Iran. The present study was designed to develop PCR assay, based on IS711 gene for rapid diagnosis of . and immediate detection of , with high sensitivity and specificity. Four pairs of oligo-nucleotide primers with sizes of 547, 403, 291 and 127bp respectively, were planned to exclusively amplify the targeted genes of Brucella species.

RESULTS

Our results show that, five PCR primers set up, would be helpful in amplifying the DNAs from the genus with high specificity and sensitivity so it can be 12 fg, for species to provide a valuable tool for diagnosis.

CONCLUSION

This method can be more useful than serological and biochemical tests and in addition, this reduces the number of required tests more rapidly and economically.

摘要

引言

布鲁氏菌病是一种全球性人畜共患病,是人类和动物健康损失的重要原因。传统上,经典诊断是通过分离[具体内容缺失]来进行的,这既耗时、技术上具有挑战性,又有潜在危险。本研究的目的是扩展一种分子检测方法,该方法通过靶向IS711元件,可在单一反应中用于高灵敏度和特异性地检测[具体内容缺失]。

方法

本研究于2015年至2016年在伊朗巴博勒的阿亚图拉·罗哈尼医院进行。本研究旨在开发基于IS711基因的PCR检测方法,用于快速诊断[具体内容缺失],并以高灵敏度和特异性即时检测[具体内容缺失]。设计了四对寡核苷酸引物,大小分别为547、403、291和127bp,专门用于扩增布鲁氏菌属的目标基因。

结果

我们的结果表明,所建立的五组PCR引物有助于以高特异性和灵敏度扩增布鲁氏菌属的DNA,其灵敏度可达12fg,为[具体内容缺失]物种的诊断提供了一种有价值的工具。

结论

该方法可能比血清学和生化检测更有用,此外,它能更快速、经济地减少所需检测的数量。

相似文献

1
Evaluation of Different Primers for Detection of by Using PCR Method.使用聚合酶链式反应(PCR)方法评估用于检测……的不同引物
Electron Physician. 2016 Nov 25;8(11):3222-3227. doi: 10.19082/3222. eCollection 2016 Nov.
2
[Comparison of conventional methods and real-time multiplex polymerase chain reaction for identification and typing of Brucella isolates of human origin].[传统方法与实时多重聚合酶链反应用于鉴定和分型人源布鲁氏菌分离株的比较]
Mikrobiyol Bul. 2011 Jul;45(3):392-400.
3
Evaluation of three polymerase chain reaction techniques for detection of Brucella DNA in peripheral human blood.三种聚合酶链反应技术检测人外周血中布鲁氏菌DNA的评估
Can J Microbiol. 2008 May;54(5):352-7. doi: 10.1139/w08-017.
4
Rapid visual isothermal nucleic acid-based detection assay of Brucella species by polymerase spiral reaction.聚合酶螺旋反应快速目视等温核酸检测布鲁氏菌属。
J Appl Microbiol. 2018 Sep;125(3):646-654. doi: 10.1111/jam.13882. Epub 2018 Jun 27.
5
Comparison of three different PCR methods for detection of Brucella spp in human blood samples.三种不同聚合酶链反应方法检测人血样本中布鲁氏菌属的比较
FEMS Immunol Med Microbiol. 2002 Oct 11;34(2):147-51. doi: 10.1111/j.1574-695X.2002.tb00616.x.
6
Serological and molecular investigation of human brucellosis in participants of Famenin brucellosis cohort study, Hamadan, Iran.伊朗哈马丹法梅宁布鲁氏菌病队列研究参与者中人类布鲁氏菌病的血清学和分子学调查
Iran J Microbiol. 2021 Jun;13(3):319-324. doi: 10.18502/ijm.v13i3.6394.
7
Real-time PCR for identification of Brucella spp.: a comparative study of IS711, bcsp31 and per target genes.用于布鲁氏菌属鉴定的实时荧光定量PCR:IS711、bcsp31和每个靶基因的比较研究
Vet Microbiol. 2009 May 28;137(1-2):156-64. doi: 10.1016/j.vetmic.2008.12.023. Epub 2009 Jan 4.
8
Establishment of a recombinase polymerase amplification (RPA) assay for the detection of Brucella spp. Infection.建立一种重组酶聚合酶扩增(RPA)检测方法,用于检测布鲁氏菌属感染。
Mol Cell Probes. 2019 Oct;47:101434. doi: 10.1016/j.mcp.2019.101434. Epub 2019 Aug 8.
9
Evaluation of PCR methods for detection of Brucella strains from culture and tissues.用于从培养物和组织中检测布鲁氏菌菌株的聚合酶链反应(PCR)方法的评估
Trop Anim Health Prod. 2017 Apr;49(4):755-763. doi: 10.1007/s11250-017-1256-1. Epub 2017 Mar 3.
10
Evaluation of genus-specific and species-specific real-time PCR assays for the identification of Brucella spp.用于鉴定布鲁氏菌属的属特异性和种特异性实时荧光定量PCR检测方法的评估
Clin Chem Lab Med. 2007;45(11):1464-70. doi: 10.1515/CCLM.2007.305.

引用本文的文献

1
Optimization and validation of a real-time polymerase chain reaction protocol for the diagnosis of human brucellosis.优化和验证实时聚合酶链反应协议在人布鲁氏菌病诊断中的应用。
Folia Microbiol (Praha). 2020 Apr;65(2):353-361. doi: 10.1007/s12223-019-00731-1. Epub 2019 Jul 31.

本文引用的文献

1
Different Clinical Presentations of Brucellosis.布鲁氏菌病的不同临床表现。
Jundishapur J Microbiol. 2016 Apr 9;9(4):e33765. doi: 10.5812/jjm.33765. eCollection 2016 Apr.
2
Frequency of sacroiliitis among patients with low back pain.腰痛患者中骶髂关节炎的发病率。
Electron Physician. 2016 Mar 25;8(3):2094-100. doi: 10.19082/2094. eCollection 2016 Mar.
3
Risk Factors for Relapse of Human Brucellosis.人类布鲁氏菌病复发的危险因素。
Glob J Health Sci. 2015 Nov 3;8(7):77-82. doi: 10.5539/gjhs.v8n7p77.
4
New developments in the diagnostic procedures for zoonotic brucellosis in humans.人类人畜共患布鲁氏菌病诊断程序的新进展。
Rev Sci Tech. 2013 Apr;32(1):177-88. doi: 10.20506/rst.32.1.2204.
5
Development and evaluation of an IS711-based loop mediated isothermal amplification method (LAMP) for detection of Brucella spp. on clinical samples.基于 IS711 的环介导等温扩增法(LAMP)的开发与评价及其在临床样本中布鲁氏菌属检测的应用。
Res Vet Sci. 2013 Oct;95(2):489-94. doi: 10.1016/j.rvsc.2013.05.002. Epub 2013 May 25.
6
Pre-analytical sample treatment and DNA extraction protocols for the detection of bacterial pathogens from whole blood.用于从全血中检测细菌病原体的分析前样本处理及DNA提取方案。
Methods Mol Biol. 2013;943:81-90. doi: 10.1007/978-1-60327-353-4_4.
7
Update on childhood brucellosis.儿童布鲁氏菌病的最新情况。
Recent Pat Antiinfect Drug Discov. 2013 Apr;8(1):42-6. doi: 10.2174/1574891x11308010008.
8
Implications of laboratory diagnosis on brucellosis therapy.实验室诊断对布鲁氏菌病治疗的影响。
Expert Rev Anti Infect Ther. 2011 Jul;9(7):833-45. doi: 10.1586/eri.11.55.
9
Evaluation of serological tests for diagnosis of brucellosis.布鲁氏菌病血清学检测方法评价。
Jpn J Infect Dis. 2011;64(4):272-6.
10
Comparison of direct culture versus PCR for the detection of Brucella in aborted fetuses of cattle and sheep in Turkey.比较直接培养和 PCR 检测土耳其牛羊流产胎儿中的布鲁氏菌。
Vet Rec. 2011 Apr 23;168(16):430. doi: 10.1136/vr.c7003. Epub 2011 Apr 14.