• 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

利用克隆的cDNA探针通过核酸杂交检测鱼类组织中的方形病毒RNA。

Detection of aquareovirus RNA in fish tissues by nucleic acid hybridization with a cloned cDNA probe.

作者信息

Subramanian K, Lupiani B, Hetrick F M, Samal S K

机构信息

College of Veterinary Medicine, University of Maryland, College Park 20742.

出版信息

J Clin Microbiol. 1993 Jun;31(6):1612-4. doi: 10.1128/jcm.31.6.1612-1614.1993.

DOI:10.1128/jcm.31.6.1612-1614.1993
PMID:8391024
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC265588/
Abstract

A nucleic acid hybridization assay was developed to rapidly detect small quantities of aquareovirus RNAs in infected cells and organs. Cloned cDNA copies were synthesized from the genomic RNA of the SBR strain of aquareovirus. By using cloned cDNA probes, aquareovirus RNAs were detected in spleen and kidney tissues of experimentally infected fish.

摘要

开发了一种核酸杂交试验,用于快速检测感染细胞和器官中的少量水生呼肠孤病毒RNA。从水生呼肠孤病毒SBR株的基因组RNA合成了克隆的cDNA拷贝。通过使用克隆的cDNA探针,在实验感染鱼的脾脏和肾脏组织中检测到了水生呼肠孤病毒RNA。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ef/265588/1f85f1e50e7e/jcm00018-0225-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ef/265588/c2e6ac9f53f9/jcm00018-0224-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ef/265588/3360dfe21b86/jcm00018-0225-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ef/265588/1f85f1e50e7e/jcm00018-0225-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ef/265588/c2e6ac9f53f9/jcm00018-0224-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ef/265588/3360dfe21b86/jcm00018-0225-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ef/265588/1f85f1e50e7e/jcm00018-0225-b.jpg

相似文献

1
Detection of aquareovirus RNA in fish tissues by nucleic acid hybridization with a cloned cDNA probe.利用克隆的cDNA探针通过核酸杂交检测鱼类组织中的方形病毒RNA。
J Clin Microbiol. 1993 Jun;31(6):1612-4. doi: 10.1128/jcm.31.6.1612-1614.1993.
2
Detection of infectious pancreatic necrosis virus (IPNV) RNA by hybridization with an oligonucleotide DNA probe.
Vet Microbiol. 1990 Jun;23(1-4):211-9. doi: 10.1016/0378-1135(90)90151-k.
3
Detection of infectious bursal disease viruses by using cloned cDNA probes.利用克隆的 cDNA 探针检测传染性法氏囊病病毒
J Clin Microbiol. 1989 Nov;27(11):2437-43. doi: 10.1128/jcm.27.11.2437-2443.1989.
4
Identification and genomic characterization of a novel fish reovirus, Hubei grass carp disease reovirus, isolated in 2009 in China.鉴定和分析一株新型鱼类呼肠孤病毒——2009 年在中国分离的草鱼出血病呼肠孤病毒。
J Gen Virol. 2013 Oct;94(Pt 10):2266-2277. doi: 10.1099/vir.0.054767-0. Epub 2013 Jul 12.
5
Characterization of a nonradioactive cloned cDNA probe for detecting avian reoviruses.
Avian Dis. 1997 Apr-Jun;41(2):374-8.
6
Identification of a new genogroup of aquareovirus by RNA-RNA hybridization.
J Gen Virol. 1997 Jun;78 ( Pt 6):1385-8. doi: 10.1099/0022-1317-78-6-1385.
7
Detection of infectious pancreatic necrosis virus using an inhibition enzyme-linked immunosorbent assay.使用抑制性酶联免疫吸附测定法检测传染性胰腺坏死病毒
J Immunoassay. 1986;7(4):229-39. doi: 10.1080/01971528608060469.
8
Development of a rapid, sensitive and specific diagnostic assay for fish Aquareovirus based on RT-PCR.基于逆转录聚合酶链反应(RT-PCR)开发一种快速、灵敏且特异的鱼类水生呼肠孤病毒诊断检测方法。
J Virol Methods. 2004 Jun 15;118(2):111-22. doi: 10.1016/j.jviromet.2004.01.023.
9
Isolation and characterization of the fall Chinook aquareovirus.秋季奇努克鲑鱼水产呼肠孤病毒的分离与鉴定
Virol J. 2017 Sep 5;14(1):170. doi: 10.1186/s12985-017-0839-9.
10
In vitro and in vivo detection of infectious pancreatic necrosis virus in fish by enzyme-linked immunosorbent assay.通过酶联免疫吸附测定法对鱼类传染性胰腺坏死病毒进行体外和体内检测。
Am J Vet Res. 1984 Sep;45(9):1876-9.

引用本文的文献

1
Antibodies against outer-capsid proteins of grass carp reovirus expressed in E. coli are capable of neutralizing viral infectivity.大肠杆菌中表达的草鱼呼肠孤病毒外壳蛋白抗体能够中和病毒感染性。
Virol J. 2011 Jul 12;8:347. doi: 10.1186/1743-422X-8-347.

本文引用的文献

1
Cloning the double-stranded RNA genes of reovirus: sequence of the cloned S2 gene.呼肠孤病毒双链RNA基因的克隆:克隆的S2基因序列
Proc Natl Acad Sci U S A. 1982 Dec;79(24):7644-8. doi: 10.1073/pnas.79.24.7644.
2
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity.一种将DNA限制性内切酶片段放射性标记至高比活度的技术。
Anal Biochem. 1983 Jul 1;132(1):6-13. doi: 10.1016/0003-2697(83)90418-9.
3
A simple and very efficient method for generating cDNA libraries.一种简单且非常有效的生成cDNA文库的方法。
Gene. 1983 Nov;25(2-3):263-9. doi: 10.1016/0378-1119(83)90230-5.
4
Sequence relatedness of Palyam virus genes to cognates of the Palyam serogroup viruses by RNA-RNA blot hybridization.通过RNA-RNA印迹杂交法检测帕利亚姆病毒基因与帕利亚姆血清群病毒同源基因的序列相关性。
Virology. 1985 May;143(1):55-62. doi: 10.1016/0042-6822(85)90096-0.
5
Heterogeneity in the genome RNAs and polypeptides of five members of a novel group of rotavirus-like viruses isolated from aquatic animals.从水生动物中分离出的一组新型轮状病毒样病毒的五个成员的基因组RNA和多肽的异质性。
J Gen Virol. 1991 Jan;72 ( Pt 1):181-4. doi: 10.1099/0022-1317-72-1-181.