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1
Broadly active inhibitor of viruses spontaneously produced by many cell types in culture.对培养中多种细胞类型自发产生的病毒具有广泛活性的抑制剂。
Infect Immun. 1981 May;32(2):449-53. doi: 10.1128/iai.32.2.449-453.1981.
2
Cell-produced viral inhibitor: possible mechanism of action and chemical composition.细胞产生的病毒抑制剂:可能的作用机制和化学成分。
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Rescue of vesicular stomatitis virus from interferon-induced resistance by superinfection with vaccinia virus. II. Effect of UV-inactivated vaccinia and metabolic inhibitors.通过痘苗病毒超感染从干扰素诱导的抗性中拯救水疱性口炎病毒。II. 紫外线灭活痘苗和代谢抑制剂的作用。
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Rescue of vesicular stomatitis virus from interferon-induced resistance by superinfection with vaccinia virus. I. Rescue in cell cultures from different species.通过痘苗病毒超感染从干扰素诱导的抗性中拯救水疱性口炎病毒。I. 在不同物种的细胞培养物中拯救
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Cell culture propagation of bovine coronavirus.牛冠状病毒的细胞培养增殖
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8
Cell-produced viral inhibitor: possible mechanism of action and chemical composition.细胞产生的病毒抑制剂:可能的作用机制和化学成分。
Infect Immun. 1981 May;32(2):454-7. doi: 10.1128/iai.32.2.454-457.1981.
9
Fetal rhesus monkey lung cells can be grown in serum-free medium for the replication of dengue-2 vaccine virus.恒河猴胎儿肺细胞可在无血清培养基中培养,用于登革2型疫苗病毒的复制。
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An influenza virus inhibitor that acts late in the replication cycle.一种在复制周期后期起作用的流感病毒抑制剂。
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本文引用的文献

1
The mammalian cell-virus relationship. II. Adsorption, reception, and eclipse of poliovirus by HeLa cells.哺乳动物细胞与病毒的关系。II. 脊髓灰质炎病毒被海拉细胞的吸附、接受和隐蔽期
J Exp Med. 1959 May 1;109(5):487-504. doi: 10.1084/jem.109.5.487.
2
Cell-produced viral inhibitor: possible mechanism of action and chemical composition.细胞产生的病毒抑制剂:可能的作用机制和化学成分。
Infect Immun. 1981 May;32(2):454-7. doi: 10.1128/iai.32.2.454-457.1981.
3
Serum inhibitors of myxoviruses.黏液病毒的血清抑制剂。
Curr Top Microbiol Immunol. 1969;47:125-51. doi: 10.1007/978-3-642-46160-6_6.
4
Antiviral action of mouse interferon in heterologous cells.小鼠干扰素在异源细胞中的抗病毒作用。
J Bacteriol. 1966 Jan;91(1):231-5. doi: 10.1128/jb.91.1.231-235.1966.
5
General considerations of the interferon system.干扰素系统的一般考量
Tex Rep Biol Med. 1977;35:1-10.
6
A microplaque reduction assay for human and mouse interferon.一种用于人和小鼠干扰素的微量空斑减少试验。
Can J Microbiol. 1975 Aug;21(8):1247-53. doi: 10.1139/m75-186.
7
Antiviral activity in milk of possible clinical importance.牛奶中具有可能具有临床重要性的抗病毒活性。
Lancet. 1976 Dec 25;2(8000):1387-9. doi: 10.1016/s0140-6736(76)91922-x.

对培养中多种细胞类型自发产生的病毒具有广泛活性的抑制剂。

Broadly active inhibitor of viruses spontaneously produced by many cell types in culture.

作者信息

Baron S, McKerlie L

出版信息

Infect Immun. 1981 May;32(2):449-53. doi: 10.1128/iai.32.2.449-453.1981.

DOI:10.1128/iai.32.2.449-453.1981
PMID:6265356
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC351464/
Abstract

A broadly active inhibitor of viruses (vaccinia, polio 1, and vesicular stomatitis) was found in the culture fluid from many types of normal human and mouse cells in culture. Virus plaque-inhibiting activity appeared in culture fluids within a few hour after incubation of cultures with fresh medium. Peak inhibitory activity occurred within 24 h. Blockade of cellular ribonucleic acid or protein synthesis decreased appearance of the inhibitor, thereby substantiating that it is a cell-produced viral inhibitor. Inhibition of virus required the simultaneous presence of inhibitor, virus, and cells (due to the reversible nature of the inhibition of virus attachment and penetration, as shown in the accompanying paper [T. K. Hughes et al., Infect Immun. 32:454-457, 1981]). The degree of inhibitory activity depended on the animal species of origin of the inhibitor, the cell type used for assay, and the virus type used for challenge. No cell species barrier against inhibitor action was found. Strong inhibition of multicycle yields of vesicular stomatitis virus and Sindbis virus was caused by low doses of inhibitor. These specific characteristics of the present inhibitor separate it from commonly recognized inhibitors. Possible biological significance of the inhibitor is discussed.

摘要

在多种正常人类和小鼠培养细胞的培养液中发现了一种对病毒(痘苗病毒、脊髓灰质炎病毒1型和水疱性口炎病毒)具有广泛活性的抑制剂。在用新鲜培养基培养细胞后的数小时内,培养液中就出现了病毒蚀斑抑制活性。最高抑制活性在24小时内出现。细胞核糖核酸或蛋白质合成的阻断减少了抑制剂的出现,从而证实它是一种细胞产生的病毒抑制剂。抑制病毒需要抑制剂、病毒和细胞同时存在(如随附论文[T.K.休斯等人,《感染与免疫》。32:454 - 457,1981]所示,这是由于病毒附着和穿透抑制的可逆性质)。抑制活性的程度取决于抑制剂来源的动物物种、用于检测的细胞类型以及用于攻击的病毒类型。未发现针对抑制剂作用的细胞物种屏障。低剂量的抑制剂对水疱性口炎病毒和辛德毕斯病毒的多轮增殖有强烈抑制作用。本抑制剂的这些特定特性使其与公认的抑制剂有所不同。文中讨论了该抑制剂可能的生物学意义。