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从一名亚急性硬化性全脑炎患者中分离并鉴定出一种缺陷型麻疹病毒。

Isolation and characterisation of a defective measles virus from a subacute sclerosing panencephalitis patient.

作者信息

Wild T F, Giraudon P, Bernard A, Huppert J

出版信息

J Med Virol. 1979;4(2):103-14. doi: 10.1002/jmv.1890040205.

DOI:10.1002/jmv.1890040205
PMID:490144
Abstract

A cytopathic measles virus was isolated from a brain biopsy of a subacute sclerosing panencephalitis (SSPE) patient. The agent could be transferred to Vero cells by cocultivation, but the infectivity always remained cell-associated -ie, a defective virus infection. The cell-associated nature of the virus was retained through 25 passages in Vero cells. Intracerebral inoculation of hamsters (2-6 days old) with the cocultured Vero cells gave rise to 100% mortality in 5-7 days. The virus retained its cell-associated nature after passage in hamsters. Electron microscopy of the brain and Vero cocultures showed the presence of virus-like ribonucleoparticles mainly in the nucleus. The presence of viral antigens in the nucleus, cytoplasm, and on the plasma membranes was confirmed by immunofluorescence. Using a combination of immunological and biochemical techniques, it was shown that all the viral proteins were synthesized with the exception of the haemagglutinin. Inclusion of the fusion inhibitor SV4814 (CBZ-D phenylalanine-L-phenylalanine-L-arginine-NO2) in the culture medium led to the elimination of the SSPE infection.

摘要

从一名亚急性硬化性全脑炎(SSPE)患者的脑活检组织中分离出一种细胞病变性麻疹病毒。该病原体可通过共培养转移至非洲绿猴肾细胞(Vero细胞),但其感染性始终与细胞相关——即存在缺陷病毒感染。该病毒与细胞的相关性在Vero细胞中传代25次后仍得以保留。用共培养的Vero细胞对仓鼠(2 - 6日龄)进行脑内接种,5 - 7天内死亡率达100%。该病毒在仓鼠体内传代后仍保持其与细胞相关的特性。对脑和Vero细胞共培养物进行电子显微镜检查显示,病毒样核糖核蛋白颗粒主要存在于细胞核中。免疫荧光法证实细胞核、细胞质和质膜上均存在病毒抗原。采用免疫和生化技术相结合的方法表明,除血凝素外,所有病毒蛋白均能合成。在培养基中加入融合抑制剂SV4814(CBZ - D - 苯丙氨酸 - L - 苯丙氨酸 - L - 精氨酸 - NO2)可消除SSPE感染。

相似文献

1
Isolation and characterisation of a defective measles virus from a subacute sclerosing panencephalitis patient.从一名亚急性硬化性全脑炎患者中分离并鉴定出一种缺陷型麻疹病毒。
J Med Virol. 1979;4(2):103-14. doi: 10.1002/jmv.1890040205.
2
Isolation and characterization of a defective measles virus from brain biopsies of three patients in Iran with subacute sclerosing panencephalitis.
Intervirology. 1978;9(2):106-18. doi: 10.1159/000148928.
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Subacute sclerosing panencephalitis (SSPE): isolation of a defective variant of measles virus from brain obtained at autopsy.亚急性硬化性全脑炎(SSPE):从尸检获得的脑组织中分离出一种缺陷型麻疹病毒变种。
Biken J. 1975 Jun;18(2):113-22.
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[Subacute sclerosing panencephalitis. A case with a prolonged course in an adult. Isolation and characteristics of a "defective" measles virus (author's transl)].
Rev Neurol (Paris). 1979 Nov;135(10):653-63.
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Electron optical investigations on the morphological alterations produced by subacute sclerosing panencephalitis (SSPE) virus in Cercopithecus aethiops (R 6 CA) kidney cells.对亚急性硬化性全脑炎(SSPE)病毒在猕猴(R 6 CA)肾细胞中引起的形态学改变进行的电子光学研究。
Rev Roum Virol (1972). 1973;10(1):33-7.
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Experimental subacute sclerosing panencephalitis: selective disappearance of measles virus matrix protein from the Central nervous system.实验性亚急性硬化性全脑炎:麻疹病毒基质蛋白在中枢神经系统中的选择性消失。
J Infect Dis. 1981 Aug;144(2):161-9. doi: 10.1093/infdis/144.2.161.
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Measles virus persistency and disease.麻疹病毒持续性与疾病
Prog Med Virol. 1984;30:44-61.
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Subacute sclerosing panencephalitis (SSPE) agent in hamsters. 3. Induction of defective measles infection in hamster brain.仓鼠中的亚急性硬化性全脑炎(SSPE)病原体。3. 仓鼠脑中缺陷性麻疹感染的诱导。
Exp Mol Pathol. 1974 Oct;21(2):166-78. doi: 10.1016/0014-4800(74)90087-2.
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Isolation and biological characterization of a measles virus-like agent from the brain of an autopsied case of subacute sclerosing panencephalitis (SSPE).
Microbiol Immunol. 1977;21(4):193-205. doi: 10.1111/j.1348-0421.1977.tb00281.x.
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Subacute sclerosing panencephalitis and defective interfering measles virus particles.亚急性硬化性全脑炎与缺陷干扰麻疹病毒颗粒
Virologie. 1980 Jan-Mar;31(1):3-8.

引用本文的文献

1
Protection of mice from fatal measles encephalitis by vaccination with vaccinia virus recombinants encoding either the hemagglutinin or the fusion protein.用编码血凝素或融合蛋白的痘苗病毒重组体对小鼠进行疫苗接种,可保护其免受致命性麻疹脑炎的侵害。
Proc Natl Acad Sci U S A. 1988 Feb;85(4):1252-6. doi: 10.1073/pnas.85.4.1252.