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本文引用的文献

1
Persistent foot-and-mouth disease infections of cells in tissue culture.组织培养中细胞的持续性口蹄疫感染。
Virology. 1959 Aug;8:542-4. doi: 10.1016/0042-6822(59)90060-1.
2
Molecular anatomy of mouse hepatitis virus persistence: coevolution of increased host cell resistance and virus virulence.小鼠肝炎病毒持续性的分子解剖学:宿主细胞抗性增加与病毒毒力的共同进化。
J Virol. 1996 Jun;70(6):3947-60. doi: 10.1128/JVI.70.6.3947-3960.1996.
3
Identification of an essential region for internal initiation of translation in the aphthovirus internal ribosome entry site and implications for viral evolution.口疮病毒内部核糖体进入位点中翻译内部起始关键区域的鉴定及其对病毒进化的意义。
J Virol. 1996 Feb;70(2):992-8. doi: 10.1128/JVI.70.2.992-998.1996.
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Molecular epidemiology of foot-and-mouth disease virus type O.
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The carrier state in foot and mouth disease--an immunological review.口蹄疫的携带状态——免疫学综述
Br Vet J. 1993 May-Jun;149(3):207-23. doi: 10.1016/S0007-1935(05)80168-X.
6
A single nucleotide substitution in the internal ribosome entry site of foot-and-mouth disease virus leads to enhanced cap-independent translation in vivo.口蹄疫病毒内部核糖体进入位点的单核苷酸替换导致体内不依赖帽子结构的翻译增强。
J Virol. 1993 Jul;67(7):3748-55. doi: 10.1128/JVI.67.7.3748-3755.1993.
7
Experimental transmission of foot-and-mouth disease virus from carrier African buffalo (Syncerus caffer) to cattle in Zimbabwe.口蹄疫病毒在津巴布韦从携带病毒的非洲水牛(非洲野水牛)传播至牛的实验性传播
Vet Rec. 1994 Feb 26;134(9):211-5. doi: 10.1136/vr.134.9.211.
8
Rapid cell variation can determine the establishment of a persistent viral infection.快速的细胞变异能够决定持续性病毒感染的形成。
Proc Natl Acad Sci U S A. 1994 Apr 26;91(9):3705-9. doi: 10.1073/pnas.91.9.3705.
9
Ultrastructural and replicative features of foot-and-mouth disease virus in persistently infected BHK-21 cells.口蹄疫病毒在持续感染的BHK - 21细胞中的超微结构和复制特征。
Arch Virol. 1995;140(1):13-25. doi: 10.1007/BF01309720.
10
The cardiovirulent phenotype of coxsackievirus B3 is determined at a single site in the genomic 5' nontranslated region.柯萨奇病毒B3的心脏毒性表型由基因组5'非翻译区的一个位点决定。
J Virol. 1995 Aug;69(8):4607-18. doi: 10.1128/JVI.69.8.4607-4618.1995.

毒力作为病毒持续性的一个积极特征。

Virulence as a positive trait in viral persistence.

作者信息

Sáiz J C, Domingo E

机构信息

Centro de Biología Molecular Severo Ochoa (CSIC-UAM), Universidad Autónoma de Madrid, Spain.

出版信息

J Virol. 1996 Sep;70(9):6410-3. doi: 10.1128/JVI.70.9.6410-6413.1996.

DOI:10.1128/JVI.70.9.6410-6413.1996
PMID:8709272
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC190670/
Abstract

A population replacement experiment has been devised to test the ability of a challenge virus to replace the resident virus in a persistently infected cell culture. BHK-21 cells persistently infected with foot-and-mouth disease virus of serotype C (clone C-S8c1) were challenged with a large excess of either the parental foot-and-mouth disease virus C-S8c1, genetically marked variants differing in their degree of virulence, or a mutant rescued after prolonged persistence in BHK-21 cells. After challenge, the composition of the resident virus population in the carrier culture was analyzed by reverse transcription-PCR amplification and nucleotide sequencing. The dominance of the initial persisting virus was seen in all cases, except when virulent viruses were used in the challenge. The experiments document that, paradoxically, virulence can be a positive factor in the reestablishment of a virus population in a persistently infected cell culture. A model based on the selection of virus-resistant cell variants during persistence is proposed to interpret these observations. Implications about the persistence of viruses in their host cells and organisms are discussed.

摘要

已设计了一项群体替代实验,以测试攻击病毒在持续感染的细胞培养物中替代驻留病毒的能力。用大量过量的亲本口蹄疫病毒C-S8c1、毒力程度不同的基因标记变体或在BHK-21细胞中长时间持续存在后拯救的突变体,对持续感染C型口蹄疫病毒(克隆C-S8c1)的BHK-21细胞进行攻击。攻击后,通过逆转录PCR扩增和核苷酸测序分析载体培养物中驻留病毒群体的组成。在所有情况下,除了在攻击中使用强毒病毒外,初始持续存在的病毒都占主导地位。这些实验证明,矛盾的是,毒力在持续感染的细胞培养物中病毒群体的重建中可能是一个积极因素。提出了一个基于在持续存在期间选择抗病毒细胞变体的模型来解释这些观察结果。讨论了关于病毒在其宿主细胞和生物体中持续存在的意义。