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Bio Protoc. 2018 May 5;8(9):e2831. doi: 10.21769/BioProtoc.2831.
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Norovirus in Transplantation.移植中的诺如病毒
Curr Infect Dis Rep. 2016 Jun;18(6):17. doi: 10.1007/s11908-016-0524-y.
2
Treatment with a Nucleoside Polymerase Inhibitor Reduces Shedding of Murine Norovirus in Stool to Undetectable Levels without Emergence of Drug-Resistant Variants.核苷聚合酶抑制剂治疗可将小鼠粪便中诺如病毒的排出量降低至检测不到的水平,且不会出现耐药变异体。
Antimicrob Agents Chemother. 2015 Dec 28;60(3):1907-11. doi: 10.1128/AAC.02198-15.
3
Norovirus infection in immunocompromised hosts.免疫功能低下宿主中的诺如病毒感染。
Clin Microbiol Infect. 2014 Aug;20(8):717-23. doi: 10.1111/1469-0691.12761.
4
A single-amino-acid change in murine norovirus NS1/2 is sufficient for colonic tropism and persistence.鼠诺如病毒 NS1/2 中的单个氨基酸变化足以使其具有结肠趋向性和持续性。
J Virol. 2013 Jan;87(1):327-34. doi: 10.1128/JVI.01864-12. Epub 2012 Oct 17.
5
Development of a reverse-genetics system for murine norovirus 3: long-term persistence occurs in the caecum and colon.建立鼠诺如病毒 3 的反向遗传学系统:长期存在于盲肠和结肠中。
J Gen Virol. 2012 Jul;93(Pt 7):1432-1441. doi: 10.1099/vir.0.042176-0. Epub 2012 Apr 11.
6
Protruding domain of capsid protein is necessary and sufficient to determine murine norovirus replication and pathogenesis in vivo.衣壳蛋白的突出结构域对于确定鼠诺如病毒在体内的复制和发病机制是必要和充分的。
J Virol. 2012 Mar;86(6):2950-8. doi: 10.1128/JVI.07038-11. Epub 2012 Jan 18.
7
Duration of norovirus excretion and the longitudinal course of viral load in norovirus-infected elderly patients.诺如病毒感染老年患者的排毒时间和病毒载量的纵向变化。
J Hosp Infect. 2010 May;75(1):42-6. doi: 10.1016/j.jhin.2009.12.016. Epub 2010 Mar 21.
8
Chronic norovirus infection in renal transplant recipients.肾移植受者中的慢性诺如病毒感染
Nephrol Dial Transplant. 2009 Mar;24(3):1051-3. doi: 10.1093/ndt/gfn693. Epub 2008 Dec 10.
9
Detection of murine norovirus 1 by using plaque assay, transfection assay, and real-time reverse transcription-PCR before and after heat exposure.在热暴露前后,通过蚀斑试验、转染试验和实时逆转录聚合酶链反应检测小鼠诺如病毒1型。
Appl Environ Microbiol. 2008 Jan;74(2):543-6. doi: 10.1128/AEM.01039-07. Epub 2007 Nov 16.
10
Murine noroviruses comprising a single genogroup exhibit biological diversity despite limited sequence divergence.尽管序列差异有限,但属于单一基因组群的鼠诺如病毒仍表现出生物学多样性。
J Virol. 2007 Oct;81(19):10460-73. doi: 10.1128/JVI.00783-07. Epub 2007 Jul 25.

评估小分子抑制剂在持续性诺如病毒感染小鼠模型中的疗效。

Assessing the Efficacy of Small Molecule Inhibitors in aMouse Model of Persistent Norovirus Infection.

作者信息

Van Dycke Jana, Neyts Johan, Rocha-Pereira Joana

机构信息

Department of Microbiology and Immunology, Rega Institute for Medical Research, Laboratory of Virology and Chemotherapy, KU Leuven - University of Leuven, Leuven, Belgium.

出版信息

Bio Protoc. 2018 May 5;8(9):e2831. doi: 10.21769/BioProtoc.2831.

DOI:10.21769/BioProtoc.2831
PMID:34286040
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8275229/
Abstract

Human norovirus is the most common cause of acute gastroenteritis worldwide, resulting in estimated mortality of ~210,000 each year, of whom most are children under the age of five. However, norovirus can infect people of all age groups. There is a risk of prolonged infection in children, the elderly and patients who are immunocompromised. To study the inhibition of persistent norovirus replication by small molecule antivirals , we used a murine norovirus CR6 strain (MNV.CR6). We demonstrated earlier that efficient small molecules can reduce viral shedding in the stool of infected mice. Here we present how to generate the MNV.CR6 virus stock, infect type I and II interferon receptor knockout AG129 mice via oral gavage, administer antivirals to mice, and quantify viral genome copies in the stool of these mice.

摘要

人诺如病毒是全球急性胃肠炎最常见的病因,估计每年导致约21万人死亡,其中大多数是五岁以下儿童。然而,诺如病毒可感染所有年龄组的人群。儿童、老年人和免疫功能低下患者存在持续感染的风险。为了研究小分子抗病毒药物对诺如病毒持续复制的抑制作用,我们使用了鼠诺如病毒CR6株(MNV.CR6)。我们之前证明,有效的小分子可以减少感染小鼠粪便中的病毒排出。在此,我们介绍如何制备MNV.CR6病毒储备液,通过口服灌胃感染I型和II型干扰素受体敲除的AG129小鼠,给小鼠施用抗病毒药物,以及定量这些小鼠粪便中的病毒基因组拷贝数。