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马尔堡病毒反向遗传学系统

Marburg Virus Reverse Genetics Systems.

作者信息

Schmidt Kristina Maria, Mühlberger Elke

机构信息

Friedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Institute of Novel and Emerging Infectious Diseases, Greifswald-Insel Riems 17493, Germany.

Department of Microbiology, School of Medicine, Boston University, 620 Albany Street, Boston, MA 02118, USA.

出版信息

Viruses. 2016 Jun 22;8(6):178. doi: 10.3390/v8060178.

DOI:10.3390/v8060178
PMID:27338448
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4926198/
Abstract

The highly pathogenic Marburg virus (MARV) is a member of the Filoviridae family and belongs to the group of nonsegmented negative-strand RNA viruses. Reverse genetics systems established for MARV have been used to study various aspects of the viral replication cycle, analyze host responses, image viral infection, and screen for antivirals. This article provides an overview of the currently established MARV reverse genetic systems based on minigenomes, infectious virus-like particles and full-length clones, and the research that has been conducted using these systems.

摘要

高致病性马尔堡病毒(MARV)是丝状病毒科的成员,属于非节段性负链RNA病毒组。为马尔堡病毒建立的反向遗传学系统已被用于研究病毒复制周期的各个方面、分析宿主反应、对病毒感染进行成像以及筛选抗病毒药物。本文概述了目前基于微型基因组、感染性病毒样颗粒和全长克隆建立的马尔堡病毒反向遗传学系统,以及使用这些系统进行的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d9b/4926198/ce2e49e08422/viruses-08-00178-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d9b/4926198/0d7e3c16d035/viruses-08-00178-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d9b/4926198/40c7b6b7eb38/viruses-08-00178-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d9b/4926198/ce2e49e08422/viruses-08-00178-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d9b/4926198/0d7e3c16d035/viruses-08-00178-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d9b/4926198/40c7b6b7eb38/viruses-08-00178-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d9b/4926198/ce2e49e08422/viruses-08-00178-g003.jpg

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本文引用的文献

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Effects of Filovirus Interferon Antagonists on Responses of Human Monocyte-Derived Dendritic Cells to RNA Virus Infection.丝状病毒干扰素拮抗剂对人单核细胞衍生树突状细胞对RNA病毒感染反应的影响。
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Structural insights into the RNA-dependent RNA polymerase complexes from highly pathogenic Marburg and Ebola viruses.对高致病性马尔堡病毒和埃博拉病毒的RNA依赖性RNA聚合酶复合物的结构见解。
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A comparative analysis of Marburg virus-infected bat and human models from public high-throughput sequencing data.基于公开高通量测序数据的马尔堡病毒感染蝙蝠和人类模型的比较分析。
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Non-Ebola Filoviruses: Potential Threats to Global Health Security.非埃博拉丝状病毒:对全球卫生安全的潜在威胁。
Viruses. 2024 Jul 23;16(8):1179. doi: 10.3390/v16081179.
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Developments in Negative-Strand RNA Virus Reverse Genetics.负链RNA病毒反向遗传学的发展
Microorganisms. 2024 Mar 11;12(3):559. doi: 10.3390/microorganisms12030559.
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Recent insights into reverse genetics of norovirus.诺如病毒反向遗传学的最新研究进展。
Virus Res. 2023 Feb;325:199046. doi: 10.1016/j.virusres.2023.199046. Epub 2023 Jan 16.
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The Interplay between Autophagy and Virus Pathogenesis-The Significance of Autophagy in Viral Hepatitis and Viral Hemorrhagic Fevers.自噬与病毒发病机制的相互作用-自噬在病毒性肝炎和病毒性出血热中的意义。
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Viruses. 2021 Sep 8;13(9):1791. doi: 10.3390/v13091791.
埃博拉和马尔堡病毒 VP35 蛋白对干扰素反应的差异调节。
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J Virol. 2015 Nov 18;90(3):1444-54. doi: 10.1128/JVI.02670-15. Print 2016 Feb 1.
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Experimental Inoculation of Egyptian Rousette Bats (Rousettus aegyptiacus) with Viruses of the Ebolavirus and Marburgvirus Genera.用埃博拉病毒属和马尔堡病毒属病毒对埃及果蝠(Rousettus aegyptiacus)进行实验性接种
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PLoS Pathog. 2015 Jun 26;11(6):e1005016. doi: 10.1371/journal.ppat.1005016. eCollection 2015 Jun.
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Comparison of the Pathogenesis of the Angola and Ravn Strains of Marburg Virus in the Outbred Guinea Pig Model.在远交系豚鼠模型中马尔堡病毒安哥拉株和拉夫恩株致病机制的比较
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Marburg virus inclusions: A virus-induced microcompartment and interface to multivesicular bodies and the late endosomal compartment.马尔堡病毒包涵体:病毒诱导的微区室,与多泡体和晚期内体区室相连。
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