• 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

丙型流感病毒重组体的分离

Isolation of influenza C virus recombinants.

作者信息

Racaniello V R, Palese P

出版信息

J Virol. 1979 Dec;32(3):1006-14. doi: 10.1128/JVI.32.3.1006-1014.1979.

DOI:10.1128/JVI.32.3.1006-1014.1979
PMID:513198
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC525950/
Abstract

Recombinants between two different influenza C viruses were isolated. In MDCK (canine kidney) cells, one strain, C/JJ/50, caused lytic plaques, whereas C/JHG/66 virus did not produce clear plaques. From a mixed infection of MDCK cells with C/JHG/66 virus and UV-inactivated C/JJ/50 virus, clones were isolated which possessed the clear-plaque phenotype. Fingerprint analyses indicated that the RNAs of parent viruses had different oligonucleotide patterns and that one of the clones derived from the mixed infection was formed by reassortment of parental genes. This recombinant clone most likely inherited RNAs 1, 2, 3, 6, and 7 from C/JGH/66 virus and RNAs 4 and 5 from C/JJ/50 virus.

摘要

分离出了两种不同丙型流感病毒之间的重组体。在犬肾(MDCK)细胞中,一种毒株C/JJ/50会产生溶菌性噬斑,而C/JHG/66病毒不会产生明显的噬斑。通过用C/JHG/66病毒和紫外线灭活的C/JJ/50病毒对MDCK细胞进行混合感染,分离出了具有明显噬斑表型的克隆。指纹分析表明,亲本病毒的RNA具有不同的寡核苷酸模式,并且混合感染产生的一个克隆是由亲本基因重配形成的。这个重组克隆很可能从C/JGH/66病毒继承了RNA 1、2、3、6和7,从C/JJ/50病毒继承了RNA 4和5。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80db/525950/adb8d49a633d/jvirol00192-0318-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80db/525950/b71a5e19f752/jvirol00192-0314-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80db/525950/d7051315521a/jvirol00192-0315-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80db/525950/01502d363d00/jvirol00192-0316-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80db/525950/adb8d49a633d/jvirol00192-0318-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80db/525950/b71a5e19f752/jvirol00192-0314-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80db/525950/d7051315521a/jvirol00192-0315-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80db/525950/01502d363d00/jvirol00192-0316-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80db/525950/adb8d49a633d/jvirol00192-0318-a.jpg

相似文献

1
Isolation of influenza C virus recombinants.丙型流感病毒重组体的分离
J Virol. 1979 Dec;32(3):1006-14. doi: 10.1128/JVI.32.3.1006-1014.1979.
2
Permanent canine kidney (MDCK) cells for isolation and plaque assay of influenza B viruses.用于乙型流感病毒分离和蚀斑测定的永生化犬肾(MDCK)细胞。
Med Microbiol Immunol. 1975 Dec 30;162(1):23-7. doi: 10.1007/BF02123574.
3
Plaque assay and primary isolation of influenza A viruses in an established line of canine kidney cells (MDCK) in the presence of trypsin.在胰蛋白酶存在的情况下,对甲型流感病毒进行蚀斑测定及在已建立的犬肾细胞系(MDCK)中进行初次分离。
Med Microbiol Immunol. 1975 Dec 30;162(1):9-14. doi: 10.1007/BF02123572.
4
Temperature-sensitive influenza A virus clones originated by a cross between A/Aichi/2/68 (H3N2) and B/Yamagata/1/73.通过A/爱知/2/68(H3N2)与B/山形/1/73杂交产生的温度敏感甲型流感病毒克隆株。
Arch Virol. 1983;75(1-2):17-27. doi: 10.1007/BF01314124.
5
Isolation and preliminary characterization of a highly cytolytic influenza B virus variant with an aberrant NS gene.一株具有异常NS基因的高细胞溶解性乙型流感病毒变体的分离与初步鉴定
Virology. 1984 Jun;135(2):515-23. doi: 10.1016/0042-6822(84)90205-8.
6
Genome analysis of influenza C viruses isolated in 1981/82 from pigs in China.对1981/82年从中国猪身上分离出的丙型流感病毒进行的基因组分析。
J Gen Virol. 1984 Nov;65 ( Pt 11):1857-72. doi: 10.1099/0022-1317-65-11-1857.
7
On the origin of the H1N1 (A/USSR/90/77) influenza virus.关于H1N1(A/苏联/90/77)流感病毒的起源
J Gen Virol. 1981 Oct;56(Pt 2):437-40. doi: 10.1099/0022-1317-56-2-437.
8
Formation and characterization of an intertypic lymphocytic choriomeningitis recombinant virus.一种不同型淋巴细胞性脉络丛脑膜炎重组病毒的形成与特性分析
J Gen Virol. 1980 Nov;51(Pt 1):213-8. doi: 10.1099/0022-1317-51-1-213.
9
Cold-adapted recombinants of influenza A virus in MDCK cells. I. Development and characterization of A/Ann Arbor/6/60 X A/Alaska/6/77 recombinant viruses.甲型流感病毒在犬肾传代细胞(MDCK)中的冷适应重组体。I. A/安阿伯/6/60 X A/阿拉斯加/6/77重组病毒的构建与特性分析
Virology. 1982 May;119(1):82-95. doi: 10.1016/0042-6822(82)90067-8.
10
The multiplication of an influenza C virus in an established line of canine kidney (MDCK) cells.丙型流感病毒在已建立的犬肾(MDCK)细胞系中的增殖。
J Gen Virol. 1978 Apr;39(1):179-81. doi: 10.1099/0022-1317-39-1-179.

引用本文的文献

1
Virion aggregation shapes infection dynamics and evolutionary potential.病毒粒子聚集塑造感染动态和进化潜力。
bioRxiv. 2025 Jul 3:2025.07.03.662980. doi: 10.1101/2025.07.03.662980.
2
Host Range, Biology, and Species Specificity of Seven-Segmented Influenza Viruses-A Comparative Review on Influenza C and D.七节段流感病毒的宿主范围、生物学特性及种属特异性——关于丙型和丁型流感的比较综述
Pathogens. 2021 Dec 5;10(12):1583. doi: 10.3390/pathogens10121583.
3
Five Novel Non-Sialic Acid-Like Scaffolds Inhibit In Vitro H1N1 and H5N2 Neuraminidase Activity of Influenza a Virus.

本文引用的文献

1
Genetic recombination for antigenic markers of antigenically different strains of influenza B virus.乙型流感病毒抗原性不同毒株抗原标记的基因重组
J Virol. 1974 Feb;13(2):347-52. doi: 10.1128/JVI.13.2.347-352.1974.
2
The relationship of the receptors of a new strain of virus to those of the mumps-NDV-influenza group.一种新型病毒株的受体与腮腺炎-新城疫病毒-流感病毒组受体之间的关系。
J Exp Med. 1950 Feb;91(2):177-84. doi: 10.1084/jem.91.2.177.
3
Identification of another epidemic respiratory disease.另一种流行性呼吸道疾病的鉴定。
五种新型非唾液酸样支架抑制甲型流感病毒 H1N1 和 H5N2 神经氨酸酶活性。
Molecules. 2020 Sep 16;25(18):4248. doi: 10.3390/molecules25184248.
4
An Influenza Virus Hemagglutinin-Based Vaccine Platform Enables the Generation of Epitope Specific Human Cytomegalovirus Antibodies.基于流感病毒血凝素的疫苗平台可产生表位特异性人巨细胞病毒抗体。
Vaccines (Basel). 2019 Jun 14;7(2):51. doi: 10.3390/vaccines7020051.
5
Influenza C virus in pre-school children with respiratory infections: retrospective analysis of data from the national influenza surveillance system in Germany, 2012 to 2014.2012 年至 2014 年德国国家流感监测系统中呼吸道感染的学龄前儿童中 C 型流感病毒:回顾性数据分析。
Euro Surveill. 2019 Mar;24(10). doi: 10.2807/1560-7917.ES.2019.24.10.1800174.
6
Influenza C in Lancaster, UK, in the winter of 2014-2015.2014-2015 年冬季英国兰卡斯特的 C 型流感。
Sci Rep. 2017 Apr 13;7:46578. doi: 10.1038/srep46578.
7
Influenza C infections in Western Australia and Victoria from 2008 to 2014.2008年至2014年西澳大利亚州和维多利亚州的丙型流感感染情况。
Influenza Other Respir Viruses. 2016 Nov;10(6):455-461. doi: 10.1111/irv.12402. Epub 2016 Jul 23.
8
Targeting the skin for microneedle delivery of influenza vaccine.针对流感疫苗的微针给药的皮肤靶向。
Adv Exp Med Biol. 2013;785:121-32. doi: 10.1007/978-1-4614-6217-0_13.
9
A seven-segmented influenza A virus expressing the influenza C virus glycoprotein HEF.一种表达丙型流感病毒糖蛋白HEF的七节段甲型流感病毒。
J Virol. 2008 Jul;82(13):6419-26. doi: 10.1128/JVI.00514-08. Epub 2008 Apr 30.
10
Genetic variability: the key problem in the prevention and therapy of RNA-based virus infections.遗传变异性:基于RNA的病毒感染预防与治疗中的关键问题。
Med Res Rev. 2003 Jul;23(4):488-518. doi: 10.1002/med.10045.
Science. 1950 Oct 27;112(2913):495-7. doi: 10.1126/science.112.2913.495.
4
The fine structure of influenza A, B and C viruses.甲型、乙型和丙型流感病毒的精细结构。
Arch Gesamte Virusforsch. 1963;12:487-95. doi: 10.1007/BF01242156.
5
A further note on 1233 influenza C virus.关于丙型流感病毒1233的进一步说明。
Arch Gesamte Virusforsch. 1951;4(4):485-500. doi: 10.1007/BF01241168.
6
A reticular structure in the wall of influenza C virus.丙型流感病毒壁中的网状结构。
J Gen Virol. 1967 Jul;1(3):297-304.
7
Replication and plaque assay of influenza virus in an established line of canine kidney cells.流感病毒在已建立的犬肾细胞系中的复制及蚀斑测定
Appl Microbiol. 1968 Apr;16(4):588-94. doi: 10.1128/am.16.4.588-594.1968.
8
On the fine structure of influenza viruses.关于流感病毒的精细结构
Arch Gesamte Virusforsch. 1967;20(1):133-6. doi: 10.1007/BF01245776.
9
Further observations on the structure of influenza viruses A and C.关于甲型和丙型流感病毒结构的进一步观察
J Gen Virol. 1969 Apr;4(3):365-70. doi: 10.1099/0022-1317-4-3-365.
10
Nucleotide sequences of two fragments from the coat-protein cistron of bacteriophage R17 ribonucleic acid.噬菌体R17核糖核酸外壳蛋白顺反子两个片段的核苷酸序列
Biochem J. 1972 Aug;128(5):993-1006. doi: 10.1042/bj1280993h.