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1
Temperature-sensitive virus derived from BHK cells persistently infected with HVJ (Sendai virus).源自持续感染HVJ(仙台病毒)的BHK细胞的温度敏感病毒。
J Virol. 1975 Jan;15(1):55-63. doi: 10.1128/JVI.15.1.55-63.1975.
2
Effects of L-glutamine deprivation on growth of HVJ (Sendai virus) in BHK cells.L-谷氨酰胺缺乏对仙台病毒(HVJ)在BHK细胞中生长的影响。
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3
Relationship between establishment of persistent infection of haemagglutinating virus of Japan and the properties of the virus.日本血凝病毒持续性感染的建立与病毒特性之间的关系
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Characterization of altered BHK cells resistant to HVJ (Sendai virus) infection.抗HVJ(仙台病毒)感染的BHK细胞变异特征分析。
J Gen Virol. 1980 Mar;47(1):193-7. doi: 10.1099/0022-1317-47-1-193.
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Temperature-sensitive phenomenon of viral maturation observed in BHK cells persistently infected with HVJ.在被HVJ持续感染的BHK细胞中观察到病毒成熟的温度敏感现象。
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Antigenic variation of HVJ (Sendai virus) HN glycoprotein detectable by monoclonal antibodies during persistent infection.在持续感染期间,通过单克隆抗体可检测到的HVJ(仙台病毒)HN糖蛋白的抗原变异。
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Characterization of the polypeptides synthesized in cells infected with a temperature-sensitive mutant derived from an HVJ (Sendai virus) carrier culture.对感染了源自HVJ(仙台病毒)载体培养物的温度敏感突变体的细胞中合成的多肽的表征。
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Effect of cytolytic infection on maintenance of resistance to HVJ (Sendai virus) in an altered BHK cell culture.溶细胞性感染对经改造的BHK细胞培养物中抗HVJ(仙台病毒)抗性维持的影响。
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Homologous interference induced by a temperature-sensitive mutant derived from an HVJ (Sendai virus) carrier culture.源自HVJ(仙台病毒)载体培养物的温度敏感突变体诱导的同源干扰。
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Host-dependent temperature-sensitive growth of HVJ (Sendai virus) wild-type in rat glioma C 6 cells.HVJ(仙台病毒)野生型在大鼠胶质瘤C6细胞中宿主依赖性温度敏感生长。
Arch Virol. 1987;94(1-2):123-33. doi: 10.1007/BF01313730.

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The properties of recombinant Sendai virus having the P gene of Sendai virus pi strain derived from BHK cells persistently infected with Sendai virus.具有源自持续感染仙台病毒的BHK细胞的仙台病毒pi株P基因的重组仙台病毒的特性。
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Genetic variation during persistent reovirus infection: presence of extragenically suppressed temperature-sensitive lesions in wild-type virus isolated from persistently infected L cells.呼肠孤病毒持续感染期间的基因变异:从持续感染的L细胞中分离出的野生型病毒中存在基因外抑制的温度敏感损伤。
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Search for Sendai 6/94 viral RNA in the antigen-free cell line Cl-C-2 isolated from human multiple sclerosis brain tissue.在从人类多发性硬化症脑组织中分离出的无抗原细胞系Cl-C-2中寻找仙台6/94病毒RNA。
Infect Immun. 1983 Aug;41(2):675-82. doi: 10.1128/iai.41.2.675-682.1983.
7
Relation of HVJ (Sendai virus) production to cell growth phase in persistently infected mouse 3T3 cells.在持续感染的小鼠3T3细胞中,仙台病毒(HVJ)产生与细胞生长阶段的关系。
Arch Virol. 1984;80(1):47-57. doi: 10.1007/BF01315293.
8
Persistent viral infections as models for research in virus chemotherapy.持续性病毒感染作为病毒化疗研究的模型。
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Growth and genetic stability of the ts-1 mutant of respiratory syncytial virus at restrictive temperatures.呼吸道合胞病毒ts-1突变体在限制温度下的生长及遗传稳定性
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Persistent infection of tissue culture cells by RNA viruses.RNA病毒对组织培养细胞的持续感染。
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本文引用的文献

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THE VIRAL CARRIER STATE IN ANIMAL CELL CULTURES.动物细胞培养中的病毒携带状态
Prog Med Virol. 1964;6:111-48.
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Application of a microtechnique to viral serological investigations.一种微技术在病毒血清学研究中的应用。
J Immunol. 1962 Mar;88:320-9.
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Use of potassium tartrate for equilibrium density-gradient centrifugation of animal viruses.
Nature. 1961 Jan 21;189:220-1. doi: 10.1038/189220a0.
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The thiobarbituric acid assay of sialic acids.唾液酸的硫代巴比妥酸测定法。
J Biol Chem. 1959 Aug;234(8):1971-5.
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Identification in a recombinant influenza virus of structural proteins derived from both parents.在重组流感病毒中鉴定出来自双亲的结构蛋白。
Virology. 1966 Nov;30(3):493-501. doi: 10.1016/0042-6822(66)90125-5.
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Studies on the assembly of Newcastle disease virus: incorporation of structural proteins into virus particles.新城疫病毒组装的研究:结构蛋白掺入病毒颗粒的过程。
J Gen Virol. 1971 Sep;12(3):239-47. doi: 10.1099/0022-1317-12-3-239.
7
Relationship between neurovirulence and temperature sensitivity of an attenuated western equine encephalitis virus.一种减毒西方马脑炎病毒的神经毒力与温度敏感性之间的关系。
Arch Gesamte Virusforsch. 1971;35(2):242-50. doi: 10.1007/BF01249716.
8
Temperature-sensitive mutants isolated from L cells persistently infected with Newcastle disease virus.从持续感染新城疫病毒的L细胞中分离出的温度敏感突变体。
J Virol. 1972 Feb;9(2):200-6. doi: 10.1128/JVI.9.2.200-206.1972.
9
Developmental sequence and intracellular sites of synthesis of three structural protein antigens of influenza A2 virus.甲型流感病毒三种结构蛋白抗原的合成发育序列及细胞内位点
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10
Temperature-sensitive virus from Aedes albopictus cells chronically infected with Sindbis virus.来自长期感染辛德毕斯病毒的白纹伊蚊细胞的温度敏感病毒。
J Virol. 1974 Feb;13(2):439-47. doi: 10.1128/JVI.13.2.439-447.1974.

源自持续感染HVJ(仙台病毒)的BHK细胞的温度敏感病毒。

Temperature-sensitive virus derived from BHK cells persistently infected with HVJ (Sendai virus).

作者信息

Kimura Y, Ito Y, Shimokata K, Nishiyama Y, Nagata I

出版信息

J Virol. 1975 Jan;15(1):55-63. doi: 10.1128/JVI.15.1.55-63.1975.

DOI:10.1128/JVI.15.1.55-63.1975
PMID:163346
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC354417/
Abstract

BHK-HVJ cells, a cell line of baby hamster kidney cells persistantly infected with HVJ (Sendai virus), started to produce infectious virus by shifting down the incubation temperature from 38 to 32 C. The virus derived from BHK-HVJ cells, designated as HJV-pB, was effectively neutralized with antibody against wild-type virus (HVJ-W) which was used for the establishment of BHK-HVJ cells. HVJ-pB replicated in eggs at 32 C, but not at 38 C, while HVJ-W grew equally well at both temperatures. When BHK cells infected with HVJ-PB were incubated at 38 C, production of infectious virus, hemagglutinin, and neuraminidase was markedly restrained, whereas a considerable amount of viral nucleocapisid and envelope antigens was detected in the cells by complement fixation tests. These viral activities became detectable immediately after temperature shift-down from 38 to 32 C even at the later stage of infection. HVJ-pB was indistinguishable from HJV-W with respect to particle size, density, and morphological characteristics, but appeared to possess a higher neuraminidase activity and was inactivated more rapidly at 50 C than HVJ-W. HVJ-pB was less cytocidal and could easily cause latent infection in BHK and mouse L cells.

摘要

BHK-HVJ细胞是一种幼仓鼠肾细胞系,持续感染HVJ(仙台病毒),通过将培养温度从38℃降至32℃开始产生感染性病毒。源自BHK-HVJ细胞的病毒,命名为HJV-pB,可被用于建立BHK-HVJ细胞的野生型病毒(HVJ-W)抗体有效中和。HJV-pB在32℃的鸡胚中复制,但在38℃时不复制,而HVJ-W在这两个温度下生长情况相同。当感染HJV-PB的BHK细胞在38℃培养时,感染性病毒、血凝素和神经氨酸酶的产生受到明显抑制,而通过补体结合试验在细胞中检测到大量病毒核衣壳和包膜抗原。即使在感染后期,从38℃降至32℃后,这些病毒活性立即变得可检测到。HJV-pB在颗粒大小、密度和形态特征方面与HJV-W无法区分,但似乎具有更高的神经氨酸酶活性,并且在50℃时比HJV-W更快失活。HJV-pB的细胞毒性较小,很容易在BHK和小鼠L细胞中引起潜伏感染。