• 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

Sensitive detection of human Caliciviridae by RT-PCR.

作者信息

Stene-Johansen K, Grinde B

机构信息

Department of Virology, National Institute of Public Health, Oslo, Norway.

出版信息

J Med Virol. 1996 Nov;50(3):207-13. doi: 10.1002/(SICI)1096-9071(199611)50:3<207::AID-JMV1>3.0.CO;2-D.

DOI:10.1002/(SICI)1096-9071(199611)50:3<207::AID-JMV1>3.0.CO;2-D
PMID:8923284
Abstract

A semi-nested reverse transcriptase-polymerase chain reaction (RT-PCR) was developed for the detection of human Caliciviridae. The method was evaluated on faecal samples from patients with gastroenteritis sent to the Norwegian National Institute of Public Health for routine diagnosis by direct electron microscopy (EM). Of 166 samples, 49 were found to contain Caliciviridae by EM, while 7 samples contained other viruses. A total of 74 samples was positive by PCR, including all the samples with EM detectable Caliciviridae, while specimens containing other agents were negative. Phylogenetic analysis of RNA sequences from 14 Norwegian samples indicated that the viruses present in Norway are evenly distributed when compared to sequences of human Caliciviridae from other countries. The PCR primers should therefore be useful for samples from other regions. The phylogenetic analysis did not cluster viruses with a calici-like morphology, but mingled them with sequences from Norwalk-like viruses, indicating that the two morphological types do not represent separate genogroups.

摘要

相似文献

1
Sensitive detection of human Caliciviridae by RT-PCR.
J Med Virol. 1996 Nov;50(3):207-13. doi: 10.1002/(SICI)1096-9071(199611)50:3<207::AID-JMV1>3.0.CO;2-D.
2
Heminested multiplex reverse transcription-PCR for detection and differentiation of Norwalk-like virus genogroups 1 and 2 in fecal samples.用于检测和区分粪便样本中诺如病毒1型和2型基因组的半巢式多重逆转录聚合酶链反应
J Clin Microbiol. 2001 Jul;39(7):2690-4. doi: 10.1128/JCM.39.7.2690-2694.2001.
3
Evaluation of the Dako IDEIA norovirus EIA assay for detection of norovirus using faecal specimens from Australian gastroenteritis outbreaks.使用来自澳大利亚肠胃炎暴发的粪便标本,评估达科IDEIA诺如病毒酶免疫分析检测法对诺如病毒的检测情况。
Pathology. 2006 Apr;38(2):157-65. doi: 10.1080/00313020600559645.
4
Sapovirus detection by quantitative real-time RT-PCR in clinical stool specimens.通过定量实时逆转录聚合酶链反应检测临床粪便标本中的札幌病毒
J Virol Methods. 2006 Jun;134(1-2):146-53. doi: 10.1016/j.jviromet.2005.12.013. Epub 2006 Jan 19.
5
Outbreaks of gastroenteritis in elderly nursing homes and retirement facilities associated with human caliciviruses.与人类杯状病毒相关的老年疗养院和退休设施中的肠胃炎暴发。
J Med Virol. 1996 Dec;50(4):335-41. doi: 10.1002/(SICI)1096-9071(199612)50:4<335::AID-JMV9>3.0.CO;2-9.
6
Multiplex real time RT-PCR for the detection and quantitation of norovirus genogroups I and II in patients with acute gastroenteritis.用于检测和定量急性肠胃炎患者中诺如病毒I型和II型基因组的多重实时逆转录聚合酶链反应。
J Clin Virol. 2005 Jun;33(2):168-71. doi: 10.1016/j.jcv.2004.12.014.
7
Development of a reverse transcription-PCR-DNA enzyme immunoassay for detection of "Norwalk-like" viruses and hepatitis A virus in stool and shellfish.用于检测粪便和贝类中“诺如样”病毒及甲型肝炎病毒的逆转录聚合酶链反应-脱氧核糖核酸酶免疫测定法的开发。
Appl Environ Microbiol. 2001 Feb;67(2):742-9. doi: 10.1128/AEM.67.2.742-749.2001.
8
Detection of small round structured viruses in stool specimens from outbreaks of gastroenteritis by electron microscopy and reverse transcription-polymerase chain reaction.通过电子显微镜和逆转录-聚合酶链反应检测肠胃炎暴发时粪便标本中的小圆结构病毒。
Acta Virol. 2000 Feb;44(1):53-5.
9
Evaluation of nine sets of PCR primers in the RNA dependent RNA polymerase region for detection and differentiation of members of the family Caliciviridae, Norwalk virus and Sapporo virus.评价九组用于检测和区分杯状病毒科成员、诺如病毒和札幌病毒的RNA依赖RNA聚合酶区域的PCR引物。
Microbiol Immunol. 2000;44(5):411-9. doi: 10.1111/j.1348-0421.2000.tb02515.x.
10
Molecular epidemiology of human calicivirus gastroenteritis outbreaks in Hungary, 1998 to 2000.1998年至2000年匈牙利人杯状病毒肠胃炎暴发的分子流行病学
J Med Virol. 2002 Nov;68(3):390-8. doi: 10.1002/jmv.10216.

引用本文的文献

1
Molecular Diagnostic Methods for Detection and Characterization of Human Noroviruses.用于检测和鉴定人诺如病毒的分子诊断方法
Open Microbiol J. 2016 Apr 14;10:78-89. doi: 10.2174/1874285801610010078. eCollection 2016.
2
Coexistence of multiple genotypes, including newly identified genotypes, in outbreaks of gastroenteritis due to Norovirus in Japan.在日本,由诺如病毒引起的肠胃炎暴发中存在多种基因型,包括新发现的基因型。
J Clin Microbiol. 2004 Jul;42(7):2988-95. doi: 10.1128/JCM.42.7.2988-2995.2004.
3
Precise characterization of norovirus (Norwalk-like virus)-specific monoclonal antibodies with broad reactivity.
具有广泛反应性的诺如病毒(诺沃克样病毒)特异性单克隆抗体的精确表征。
J Clin Microbiol. 2003 Jun;41(6):2367-71. doi: 10.1128/JCM.41.6.2367-2371.2003.
4
Diagnosis of noncultivatable gastroenteritis viruses, the human caliciviruses.不可培养的肠胃炎病毒——人杯状病毒的诊断
Clin Microbiol Rev. 2001 Jan;14(1):15-37. doi: 10.1128/CMR.14.1.15-37.2001.
5
Major change in the predominant type of "Norwalk-like viruses" in outbreaks of acute nonbacterial gastroenteritis in Osaka City, Japan, between April 1996 and March 1999.1996年4月至1999年3月期间,日本大阪市急性非细菌性胃肠炎暴发中“诺如病毒样病毒”主要类型的重大变化。
J Clin Microbiol. 2000 Jul;38(7):2649-54. doi: 10.1128/JCM.38.7.2649-2654.2000.