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本文引用的文献

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Human genome-wide RNAi screen reveals a role for nuclear pore proteins in poxvirus morphogenesis.人类全基因组 RNAi 筛选揭示核孔蛋白在痘病毒形态发生中的作用。
Proc Natl Acad Sci U S A. 2013 Feb 26;110(9):3519-24. doi: 10.1073/pnas.1300708110. Epub 2013 Feb 11.
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Viral bacterial artificial chromosomes: generation, mutagenesis, and removal of mini-F sequences.病毒细菌人工染色体:微型F序列的产生、诱变及去除
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Emergence and reemergence of smallpox: the need for development of a new generation smallpox vaccine.天花的出现和再现:需要开发新一代天花疫苗。
Vaccine. 2011 Dec 30;29 Suppl 4:D49-53. doi: 10.1016/j.vaccine.2011.05.037. Epub 2011 Dec 18.
4
Cowpox virus serpin CrmA is necessary but not sufficient for the red pock phenotype on chicken chorioallantoic membranes.牛痘病毒丝氨酸蛋白酶抑制剂 CrmA 对于鸡胚绒毛尿囊膜上的红色痘斑表型是必要的,但不是充分的。
Virus Res. 2012 Jan;163(1):254-61. doi: 10.1016/j.virusres.2011.10.002. Epub 2011 Oct 12.
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Orthopoxvirus genome evolution: the role of gene loss.正痘病毒基因组进化:基因缺失的作用。
Viruses. 2010 Sep;2(9):1933-1967. doi: 10.3390/v2091933. Epub 2010 Sep 15.
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Expression profiling of the intermediate and late stages of poxvirus replication.痘病毒复制的中晚期表达谱分析。
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Recovery of infectious virus from full-length cowpox virus (CPXV) DNA cloned as a bacterial artificial chromosome (BAC).从全长牛痘病毒 (CPXV) DNA 克隆为细菌人工染色体 (BAC) 中回收感染性病毒。
Vet Res. 2011 Jan 11;42(1):3. doi: 10.1186/1297-9716-42-3.
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En passant mutagenesis: a two step markerless red recombination system.逐代诱变:一种两步无标记红色重组系统。
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9
Introduction of the six major genomic deletions of modified vaccinia virus Ankara (MVA) into the parental vaccinia virus is not sufficient to reproduce an MVA-like phenotype in cell culture and in mice.将改良安卡拉痘苗病毒(MVA)的六大基因组缺失引入亲本痘苗病毒中,不足以在细胞培养和小鼠中再现类似 MVA 的表型。
J Virol. 2010 Oct;84(19):9907-19. doi: 10.1128/JVI.00756-10. Epub 2010 Jul 28.
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Repulsion of superinfecting virions: a mechanism for rapid virus spread.排斥超感染病毒:一种快速病毒传播的机制。
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牛痘病毒完整单基因敲除细菌人工染色体文库的构建及其必需基因的鉴定。

Generation of a complete single-gene knockout bacterial artificial chromosome library of cowpox virus and identification of its essential genes.

作者信息

Xu Zhiyong, Zikos Dimitrios, Osterrieder Nikolaus, Tischer B Karsten

机构信息

Institut für Virologie, Freie Universität Berlin, Zentrum für Infektionsmedizin, Berlin, Germany.

出版信息

J Virol. 2014 Jan;88(1):490-502. doi: 10.1128/JVI.02385-13. Epub 2013 Oct 23.

DOI:10.1128/JVI.02385-13
PMID:24155400
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3911729/
Abstract

Cowpox virus (CPXV) belongs to the genus Orthopoxvirus in the Poxviridae family. It infects a broad range of vertebrates and can cause zoonotic infections. CPXV has the largest genome among the orthopoxviruses and is therefore considered to have the most complete set of genes of all members of the genus. Since CPXV has also become a model for studying poxvirus genetics and pathogenesis, we created and characterized a complete set of single gene knockout bacterial artificial chromosome (BAC) clones of the CPXV strain Brighton Red. These mutants allow a systematic assessment of the contribution of single CPXV genes to the outcome of virus infection and replication, as well as to the virus host range. A full-length BAC clone of CPXV strain Brighton Red (pBRF) harboring the gene expressing the enhanced green fluorescent protein under the control of a viral late promoter was modified by introducing the mrfp1 gene encoding the monomeric red fluorescent protein driven by a synthetic early vaccinia virus promoter. Based on the modified BAC (pBRFseR), a library of targeted knockout mutants for each single viral open reading frame (ORF) was generated. Reconstitution of infectious virus was successful for 109 of the 183 mutant BAC clones, indicating that the deleted genes are not essential for virus replication. In contrast, 74 ORFs were identified as essential because no virus progeny was obtained upon transfection of the mutant BAC clones and in the presence of a helper virus. More than 70% of all late CPXV genes belonged to this latter group of essential genes.

摘要

牛痘病毒(CPXV)属于痘病毒科正痘病毒属。它能感染多种脊椎动物,并可引起人畜共患感染。CPXV在正痘病毒中拥有最大的基因组,因此被认为拥有该属所有成员中最完整的基因集。由于CPXV也已成为研究痘病毒遗传学和发病机制的模型,我们构建并鉴定了CPXV布莱顿红株的一套完整的单基因敲除细菌人工染色体(BAC)克隆。这些突变体能够系统地评估单个CPXV基因对病毒感染和复制结果以及病毒宿主范围的贡献。携带在病毒晚期启动子控制下表达增强型绿色荧光蛋白基因的CPXV布莱顿红株全长BAC克隆(pBRF),通过引入由合成的早期痘苗病毒启动子驱动的编码单体红色荧光蛋白的mrfp1基因进行了修饰。基于修饰后的BAC(pBRFseR),生成了针对每个单个病毒开放阅读框(ORF)的靶向敲除突变体文库。183个突变BAC克隆中有109个成功重建了感染性病毒,这表明缺失的基因对病毒复制并非必需。相比之下,74个ORF被确定为必需基因,因为在转染突变BAC克隆并存在辅助病毒的情况下未获得病毒后代。所有晚期CPXV基因中超过70%属于后一组必需基因。