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本文引用的文献

1
Evaluation of cross-protection of bluetongue virus serotype 4 with other serotypes in sheep.绵羊中蓝舌病病毒4型与其他血清型交叉保护性的评估。
J S Afr Vet Assoc. 2014 Oct 16;85(1):1041. doi: 10.4102/jsava.v85i1.1041.
2
Evidence of transplacental transmission of bluetongue virus serotype 8 in goats.蓝舌病病毒血清型 8 经胎盘传播的证据在山羊中。
Vet Microbiol. 2013 Oct 25;166(3-4):394-404. doi: 10.1016/j.vetmic.2013.06.020. Epub 2013 Jul 6.
3
Experimental infection of white-tailed deer (Odocoileus virginianus) with Northern European bluetongue virus serotype 8.白尾鹿(Odocoileus virginianus)感染北欧型 8 型蓝舌病病毒的实验。
Vet Microbiol. 2013 Oct 25;166(3-4):347-55. doi: 10.1016/j.vetmic.2013.05.027. Epub 2013 Jun 19.
4
Comparative study of clinical courses, gross lesions, acute phase response and coagulation disorders in sheep inoculated with bluetongue virus serotype 1 and 8.蓝舌病病毒血清型 1 型和 8 型感染绵羊的临床过程、大体病变、急性期反应和凝血障碍的比较研究。
Vet Microbiol. 2013 Sep 27;166(1-2):184-94. doi: 10.1016/j.vetmic.2013.05.032. Epub 2013 Jun 19.
5
Rapid generation of replication-deficient monovalent and multivalent vaccines for bluetongue virus: protection against virulent virus challenge in cattle and sheep.快速生成复制缺陷型单价和多价蓝舌病毒疫苗:对牛和羊的强毒攻击的保护。
J Virol. 2013 Sep;87(17):9856-64. doi: 10.1128/JVI.01514-13. Epub 2013 Jul 3.
6
Protection of IFNAR (-/-) mice against bluetongue virus serotype 8, by heterologous (DNA/rMVA) and homologous (rMVA/rMVA) vaccination, expressing outer-capsid protein VP2.通过表达外壳蛋白 VP2 的异源(DNA/rMVA)和同源(rMVA/rMVA)疫苗接种,保护 IFNAR(-/-)小鼠免受 8 型蓝舌病毒的侵害。
PLoS One. 2013 Apr 12;8(4):e60574. doi: 10.1371/journal.pone.0060574. Print 2013.
7
Transplacental infection in goats experimentally infected with a European strain of bluetongue virus serotype 8.经实验感染欧洲 8 型蓝舌病病毒的山羊的胎盘感染。
Vet J. 2013 Aug;197(2):335-41. doi: 10.1016/j.tvjl.2013.01.005. Epub 2013 Feb 17.
8
An investigation into the possibility of bluetongue virus transmission by transfer of infected ovine embryos.关于通过转移受感染的绵羊胚胎传播蓝舌病病毒可能性的调查。
Onderstepoort J Vet Res. 2011 Feb 21;78(1):17. doi: 10.4102/ojvr.v78i1.17.
9
Determination of the minimum protective dose for bluetongue virus serotype 2 and 8 vaccines in sheep.绵羊蓝舌病病毒2型和8型疫苗最小保护剂量的测定
J S Afr Vet Assoc. 2012 Aug 3;83(1):17. doi: 10.4102/jsava.v83i1.17.
10
Reassortment between two serologically unrelated bluetongue virus strains is flexible and can involve any genome segment.两种血清学上无关的蓝舌病毒株之间的重配是灵活的,可以涉及任何基因组片段。
J Virol. 2013 Jan;87(1):543-57. doi: 10.1128/JVI.02266-12. Epub 2012 Oct 24.

哺乳动物宿主感染蓝舌病病毒的实验性研究综述。

A review of experimental infections with bluetongue virus in the mammalian host.

作者信息

Coetzee Peter, van Vuuren Moritz, Venter Estelle H, Stokstad Maria

机构信息

Department of Veterinary Tropical Diseases, Faculty of Veterinary Science, University of Pretoria, Private Bag X04, Onderstepoort, Pretoria 0110, South Africa; Department of Production Animal Clinical Sciences, Norwegian School of Veterinary Science, P. O. Box 8146 Dep., N-0033 Oslo, Norway.

Department of Veterinary Tropical Diseases, Faculty of Veterinary Science, University of Pretoria, Private Bag X04, Onderstepoort, Pretoria 0110, South Africa.

出版信息

Virus Res. 2014 Mar;182:21-34. doi: 10.1016/j.virusres.2013.12.044. Epub 2014 Jan 24.

DOI:10.1016/j.virusres.2013.12.044
PMID:24462840
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7132480/
Abstract

Experimental infection studies with bluetongue virus (BTV) in the mammalian host have a history that stretches back to the late 18th century. Studies in a wide range of ruminant and camelid species as well as mice have been instrumental in understanding BTV transmission, bluetongue (BT) pathogenicity/pathogenesis, viral virulence, the induced immune response, as well as reproductive failures associated with BTV infection. These studies have in many cases been complemented by in vitro studies with BTV in different cell types in tissue culture. Together these studies have formed the basis for the understanding of BTV-host interaction and have contributed to the design of successful control strategies, including the development of effective vaccines. This review describes some of the fundamental and contemporary infection studies that have been conducted with BTV in the mammalian host and provides an overview of the principal animal welfare issues that should be considered when designing experimental infection studies with BTV in in vivo infection models. Examples are provided from the authors' own laboratory where the three Rs (replacement, reduction and refinement) have been implemented in the design of experimental infection studies with BTV in mice and goats. The use of the ARRIVE guidelines for the reporting of data from animal infection studies is emphasized.

摘要

在哺乳动物宿主中进行的蓝舌病毒(BTV)实验性感染研究的历史可以追溯到18世纪后期。对多种反刍动物、骆驼科动物以及小鼠的研究,有助于理解BTV的传播、蓝舌病(BT)的致病性/发病机制、病毒毒力、诱导的免疫反应以及与BTV感染相关的繁殖失败。在许多情况下,这些研究通过在组织培养中对不同细胞类型进行BTV的体外研究得到了补充。这些研究共同构成了理解BTV与宿主相互作用的基础,并为成功控制策略的设计做出了贡献,包括有效疫苗的开发。本综述描述了一些在哺乳动物宿主中进行的关于BTV的基础和当代感染研究,并概述了在体内感染模型中设计BTV实验性感染研究时应考虑的主要动物福利问题。作者自己的实验室提供了一些例子,即在小鼠和山羊中设计BTV实验性感染研究时实施了3R原则(替代、减少和优化)。强调了使用ARRIVE指南报告动物感染研究数据的重要性。