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Molecular basis of reovirus virulence. Role of the M2 gene.呼肠孤病毒毒力的分子基础。M2基因的作用。
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10
Aerosol stability of infectious and potentially infectious reovirus particles.传染性和潜在传染性呼肠孤病毒颗粒的气溶胶稳定性。
Appl Environ Microbiol. 1982 Oct;44(4):903-8. doi: 10.1128/aem.44.4.903-908.1982.

本文引用的文献

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THE SECONDARY STRUCTURE OF REOVIRUS RNA.呼肠孤病毒RNA的二级结构
Proc Natl Acad Sci U S A. 1963 May;49(5):707-14. doi: 10.1073/pnas.49.5.707.
2
ELECTRON MICROSCOPY OF RNA FROM REOVIRUS AND WOUND TUMOR VIRUS.呼肠孤病毒和伤瘤病毒RNA的电子显微镜观察
J Mol Biol. 1964 Nov;10:282-8. doi: 10.1016/s0022-2836(64)80046-2.
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EFFECT OF ANTIMITOTIC AGENTS ON INTRACELLULAR REOVIRUS ANTIGEN.抗有丝分裂剂对细胞内呼肠孤病毒抗原的作用。
Cancer Res. 1964 Nov;24:1826-33.
4
STUDIES ON FILTRATES FROM CULTURES OF A PSYCHROPHILIC PSEUDOMONAS SP. WHICH INACTIVATE NONSPECIFIC SERUM INHIBITORS FOR CERTAIN HEMAGGLUTINATING VIRUSES.嗜冷假单胞菌属一种菌株培养滤液的研究,该滤液可使某些血凝病毒的非特异性血清抑制剂失活。
J Immunol. 1964 Jul;93:140-7.
5
REOVIRUS ACTIVATION BY HEATING AND INACTIVATION BY COOLING IN MGC12 SOLUTIONS.呼肠孤病毒在MGC12溶液中的加热激活及冷却灭活
Virology. 1964 Apr;22:608-19. doi: 10.1016/0042-6822(64)90083-2.
6
ISOLATION OF A REOVIRUS FROM A CASE OF BURKITT'S LYMPHOMA.从一例伯基特淋巴瘤病例中分离出呼肠孤病毒。
Br Med J. 1964 May 9;1(5392):1212-3. doi: 10.1136/bmj.1.5392.1212.
7
THE ROLE OF THE MITOTIC APPARATUS IN THE INTRACELLULAR LOCATION OF REOVIRUS ANTIGEN.有丝分裂器在呼肠孤病毒抗原细胞内定位中的作用
J Immunol. 1963 Apr;90:554-60.
8
DEVELOPMENT OF VIRAL ANTIGEN AND INFECTIOUS VIRUS IN HELA CELLS INFECTED WITH REOVIRUS.呼肠孤病毒感染的Hela细胞中病毒抗原和传染性病毒的发育
J Immunol. 1963 Apr;90:548-53.
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Cationic stabilization--a new property of enteroviruses.阳离子稳定作用——肠道病毒的一种新特性。
Virology. 1962 Apr;16:504-6. doi: 10.1016/0042-6822(62)90234-9.
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Hemagglutination with reoviruses.呼肠孤病毒引起的血细胞凝集
Virology. 1963 Jan;19:58-65. doi: 10.1016/0042-6822(63)90024-2.

呼肠孤病毒感染性的酶促增强作用

ENZYMATIC ENHANCEMENT OF INFECTIVITY OF REOVIRUS.

作者信息

SPENDLOVE R S, SCHAFFER F L

出版信息

J Bacteriol. 1965 Mar;89(3):597-602. doi: 10.1128/jb.89.3.597-602.1965.

DOI:10.1128/jb.89.3.597-602.1965
PMID:14273633
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC277508/
Abstract

Spendlove, R. S. (California State Department of Public Health, Berkeley), and F. L. Schaffer. Enzymatic enhancement of infectivity of reovirus. J. Bacteriol. 89:597-602. 1965.-Enhancement of infectivity by chymotrypsin treatment has been demonstrated with all three types of reovirus, although not in all viral preparations. Enzyme treatment did not produce a simultaneous increase in the hemagglutinating activity of reovirus type 1 (the only type tested). The infectivity of reovirus type 1 (Lang strain) was increased by treatment with chymotrypsin, trypsin, papain, and a filtrate from a culture of a Pseudomonas sp. but not by treatment with pepsin. Sedimentation experiments showed that the property of enhanceability was closely associated with the virus particles themselves. Results of studies involving various sequential treatments with chymotrypsin, and with heat in the presence or absence of 2 m MgCl(2), were compatible with the interpretation that inhibited virus is resistant to exposure to a temperature of 56 C in the absence of MgCl(2), whereas activated virus is thermolabile. Activation of reovirus infectivity by heat in the presence of MgCl(2) and by chymotrypsin was not additive.

摘要

斯彭德洛夫,R.S.(加利福尼亚州公共卫生部,伯克利)和F.L.谢弗。胰凝乳蛋白酶增强呼肠孤病毒的感染性。《细菌学杂志》89:597 - 602。1965年。——已证明用胰凝乳蛋白酶处理可增强所有三种类型呼肠孤病毒的感染性,不过并非在所有病毒制剂中都如此。酶处理并未使1型呼肠孤病毒(唯一测试的类型)的血凝活性同时增加。用胰凝乳蛋白酶、胰蛋白酶、木瓜蛋白酶以及一种假单胞菌属培养物的滤液处理可增强1型呼肠孤病毒(朗株)的感染性,但用胃蛋白酶处理则无此效果。沉降实验表明,可增强性这一特性与病毒颗粒本身密切相关。涉及用胰凝乳蛋白酶以及在有或无2 m MgCl₂存在下加热进行各种顺序处理的研究结果符合以下解释:在无MgCl₂时,受抑制的病毒对暴露于56℃温度具有抗性,而活化的病毒对热不稳定。在MgCl₂存在下加热和用胰凝乳蛋白酶对呼肠孤病毒感染性的激活并非相加的。