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1
Viruses isolated from cells persistently infected with vesicular stomatitis virus show altered interactions with defective interfering particles.从持续感染水疱性口炎病毒的细胞中分离出的病毒,与缺陷干扰颗粒的相互作用发生了改变。
J Virol. 1980 Nov;36(2):627-31. doi: 10.1128/JVI.36.2.627-631.1980.
2
Reconstruction experiments demonstrating selective effects of defective interfering particles on mixed populations of vesicular stomatitis virus.重建实验证明缺陷干扰颗粒对水疱性口炎病毒混合群体的选择性作用。
J Gen Virol. 1984 Apr;65 ( Pt 4):819-23. doi: 10.1099/0022-1317-65-4-819.
3
Defective interfering particles of vesicular stomatitis virus: structure-function relationships.水疱性口炎病毒的缺陷干扰颗粒:结构与功能的关系
Ann N Y Acad Sci. 1980;354:238-50. doi: 10.1111/j.1749-6632.1980.tb27970.x.
4
Persistent vesicular stomatitis virus infection mediates base substitutions in viral RNA termini.持续性水泡性口炎病毒感染介导病毒RNA末端的碱基替换。
J Virol. 1979 Nov;32(2):420-8. doi: 10.1128/JVI.32.2.420-428.1979.
5
Effect of defective interfering particles on plus- and minus- strand leader RNAs in vesicular stomatitis virus-infected cells.缺陷干扰颗粒对感染水疱性口炎病毒的细胞中正链和负链前导RNA的影响。
J Virol. 1980 Sep;35(3):704-9. doi: 10.1128/JVI.35.3.704-709.1980.
6
Continuing coevolution of virus and defective interfering particles and of viral genome sequences during undiluted passages: virus mutants exhibiting nearly complete resistance to formerly dominant defective interfering particles.在未稀释传代过程中病毒与缺陷干扰颗粒以及病毒基因组序列的持续协同进化:表现出对先前占主导地位的缺陷干扰颗粒几乎完全抗性的病毒突变体。
J Virol. 1987 Feb;61(2):454-64. doi: 10.1128/JVI.61.2.454-464.1987.
7
Inhibition of vesicular stomatitis virus-defective interfering particle synthesis by Shope fibroma virus.肖普纤维瘤病毒对水疱性口炎病毒缺陷干扰颗粒合成的抑制作用
Virology. 1979 Mar;93(2):515-26. doi: 10.1016/0042-6822(79)90254-x.
8
Ultraviolet-irradiated vesicular stomatitis virus and defective-interfering particles are similar non-specific inhibitors of virus infection.紫外线照射的水疱性口炎病毒和缺陷干扰颗粒是类似的病毒感染非特异性抑制剂。
J Gen Virol. 1982 Jun;60(Pt 2):327-33. doi: 10.1099/0022-1317-60-2-327.
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The intracellular half-lives of nonreplicating nucleocapsids of DI particles of wild type and mutant strains of vesicular stomatitis virus.水泡性口炎病毒野生型和突变株DI颗粒非复制核衣壳的细胞内半衰期。
Virology. 1986 Jun;151(2):371-8. doi: 10.1016/0042-6822(86)90057-7.
10
Altered replicase specificity is responsible for resistance to defective interfering particle interference of an Sdi- mutant of vesicular stomatitis virus.复制酶特异性的改变导致水泡性口炎病毒Sdi-突变体对缺陷干扰颗粒干扰产生抗性。
J Virol. 1988 Oct;62(10):3614-21. doi: 10.1128/JVI.62.10.3614-3621.1988.

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A measles virus collective infectious unit that caused lethal human brain disease includes many locally restricted and few widespread copy-back defective genomes.一种引起致命人类脑部疾病的麻疹病毒集体感染单位,包含许多局部受限和少数广泛传播的复制缺陷基因组。
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Repeatable Population Dynamics among Vesicular Stomatitis Virus Lineages Evolved under High Co-infection.在高共感染情况下进化的水疱性口炎病毒谱系间可重复的种群动态
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Defective interfering influenza virus RNAs: time to reevaluate their clinical potential as broad-spectrum antivirals?缺陷干扰流感病毒 RNA:重新评估其作为广谱抗病毒药物的临床潜力的时机?
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Design requirements for interfering particles to maintain coadaptive stability with HIV-1.干扰粒子与 HIV-1 保持共适应稳定性的设计要求。
J Virol. 2013 Feb;87(4):2081-93. doi: 10.1128/JVI.02741-12. Epub 2012 Dec 5.
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Defective interfering influenza virus confers only short-lived protection against influenza virus disease: evidence for a role for adaptive immunity in DI virus-mediated protection in vivo.缺陷干扰流感病毒只能提供短暂的流感病毒疾病保护:适应性免疫在体内 DI 病毒介导的保护中的作用证据。
Vaccine. 2011 Sep 2;29(38):6584-91. doi: 10.1016/j.vaccine.2011.06.114. Epub 2011 Jul 14.
6
Defective interfering particles of Sindbis virus do not interfere with the homologous virus obtained from persistently infected BHK cells but do interfere with Semliki Forest virus.辛德毕斯病毒的缺陷干扰颗粒不会干扰从持续感染的BHK细胞中获得的同源病毒,但会干扰Semliki森林病毒。
J Virol. 1981 Feb;37(2):840-4. doi: 10.1128/JVI.37.2.840-844.1981.
7
Evolution of virus and defective-interfering RNAs in BHK cells persistently infected with Sindbis virus.辛德毕斯病毒持续感染的BHK细胞中病毒和缺陷干扰RNA的进化
J Virol. 1983 Dec;48(3):676-84. doi: 10.1128/JVI.48.3.676-684.1983.
8
Vesicular stomatitis virus mutants resistant to defective-interfering particles accumulate stable 5'-terminal and fewer 3'-terminal mutations in a stepwise manner.对缺陷干扰颗粒具有抗性的水疱性口炎病毒突变体以逐步方式积累稳定的5'-末端和较少的3'-末端突变。
J Virol. 1984 Mar;49(3):793-8. doi: 10.1128/JVI.49.3.793-798.1984.
9
Continuing coevolution of virus and defective interfering particles and of viral genome sequences during undiluted passages: virus mutants exhibiting nearly complete resistance to formerly dominant defective interfering particles.在未稀释传代过程中病毒与缺陷干扰颗粒以及病毒基因组序列的持续协同进化:表现出对先前占主导地位的缺陷干扰颗粒几乎完全抗性的病毒突变体。
J Virol. 1987 Feb;61(2):454-64. doi: 10.1128/JVI.61.2.454-464.1987.
10
Molecular basis for interference of defective interfering particles of pseudorabies virus with replication of standard virus.伪狂犬病病毒缺陷干扰颗粒干扰标准病毒复制的分子基础。
J Virol. 1986 Aug;59(2):308-17. doi: 10.1128/JVI.59.2.308-317.1986.

本文引用的文献

1
BIOLOGIC PROPERTIES OF TWO PLAQUE VARIANTS OF VESICULAR STOMATITIS VIRUS (INDIANA SEROTYPE).水泡性口炎病毒(印第安纳血清型)两种蚀斑变体的生物学特性
J Immunol. 1963 Jul;91:112-22.
2
Some properties of the transmissible interfering component of vesicular stomatitis virus preparations.水疱性口炎病毒制剂的可传播干扰成分的一些特性。
J Gen Microbiol. 1959 Dec;21:498-509. doi: 10.1099/00221287-21-3-498.
3
Establishment and maintenance of persistent infection by Sindbis virus in BHK cells.辛德毕斯病毒在BHK细胞中持续感染的建立与维持
J Virol. 1980 Jan;33(1):463-74. doi: 10.1128/JVI.33.1.463-474.1980.
4
Semliki forest virus persistence in mouse L929 cells.辛德毕斯病毒在小鼠L929细胞中的持续性。
Virology. 1980 Jan 15;100(1):141-55. doi: 10.1016/0042-6822(80)90560-7.
5
Virus protein changes and RNA termini alterations evolving during persistent infection.在持续感染过程中发生的病毒蛋白变化和RNA末端改变。
Cell. 1980 Apr;19(4):871-80. doi: 10.1016/0092-8674(80)90078-1.
6
Defective viral particles and viral disease processes.有缺陷的病毒颗粒与病毒疾病过程。
Nature. 1970 Apr 25;226(5243):325-7. doi: 10.1038/226325a0.
7
Temperature-sensitive defect of mutants isolated from L cells persistently infected with Newcastle disease virus.从持续感染新城疫病毒的L细胞中分离出的突变体的温度敏感缺陷。
J Virol. 1973 Sep;12(3):472-80. doi: 10.1128/JVI.12.3.472-480.1973.
8
Persistent noncytocidal vesicular stomatitis virus infections mediated by defective T particles that suppress virion transcriptase.由抑制病毒粒子转录酶的缺陷型T颗粒介导的持续性非杀细胞性水疱性口炎病毒感染。
Proc Natl Acad Sci U S A. 1974 Aug;71(8):2956-60. doi: 10.1073/pnas.71.8.2956.
9
Natural selection of mutants of vesicular stomatitis virus by cultured cells of Drosophila melanogaster.黑腹果蝇培养细胞对水泡性口炎病毒突变体的自然选择。
J Gen Virol. 1973 Sep;20(3):341-51. doi: 10.1099/0022-1317-20-3-341.
10
Prophylaxis and immunization in mice by use of virus-free defective T particles to protect against intracerebral infection by vesicular stomatitis virus.通过使用无病毒缺陷T颗粒对小鼠进行预防和免疫,以防止其受到水疱性口炎病毒的脑内感染。
Proc Natl Acad Sci U S A. 1973 Jul;70(7):2105-8. doi: 10.1073/pnas.70.7.2105.

从持续感染水疱性口炎病毒的细胞中分离出的病毒,与缺陷干扰颗粒的相互作用发生了改变。

Viruses isolated from cells persistently infected with vesicular stomatitis virus show altered interactions with defective interfering particles.

作者信息

Horodyski F M, Holland J J

出版信息

J Virol. 1980 Nov;36(2):627-31. doi: 10.1128/JVI.36.2.627-631.1980.

DOI:10.1128/JVI.36.2.627-631.1980
PMID:6253684
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC353685/
Abstract

Virus mutants isolated from persistent infections of vesicular stomatitis virus in BHK-21 cells were much less susceptible to interference mediated by the defective interfering particle used to establish the persistent infection. This mutational change occurred as early as 34 days in the persistent infection and continued for over 5 years. The earliest variants showed no oligonucleotide map changes and no difference in the temperature-sensitive phenotype from the original virus, but the later variants exhibited extensive map changes. These results suggest a possible role for defective interfering particles in the selection of the mutants.

摘要

从水泡性口炎病毒在BHK - 21细胞中的持续感染中分离出的病毒突变体,对用于建立持续感染的缺陷干扰颗粒介导的干扰作用的敏感性要低得多。这种突变变化早在持续感染的第34天就出现了,并持续了5年多。最早的变体在寡核苷酸图谱上没有变化,温度敏感表型与原始病毒也没有差异,但后来的变体表现出广泛的图谱变化。这些结果表明缺陷干扰颗粒在突变体的选择中可能起作用。