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豚鼠培养细胞中巨细胞病毒和逆转录病毒假型的展示。

Demonstration of cytomegalovirus and retrovirus pseudotypes in cultured guinea pig cells.

作者信息

Lerner-Tung M B, Crouch J Y, Hsiung G D

机构信息

Yale University School of Medicine, Department of Laboratory Medicine, New Haven, Connecticut 06510.

出版信息

Virology. 1991 Feb;180(2):826-30. doi: 10.1016/0042-6822(91)90101-g.

Abstract

A mixed viral infection with a cytomegalovirus and a retrovirus in cultured guinea pig embryo (GPE) cells was investigated. The expression of an endogenous guinea pig retrovirus (GPRV) in cultured guinea pig cells was induced by a medium containing 5-bromo-2'-deoxyuridine and dexamethasone. When the induced GPE cells were superinfected with a guinea pig cytomegalovirus (GPCMV), pseudotype virions were observed. Morphological characterization of both viruses and their locations within infected cells was achieved by examination of thin sections of infected cells with transmission electron microscopy. Immunolabeling with colloidal gold particles, 5 or 15 nm in size, permitted the identification of each virus type using GPCMV- or GPRV-specific polyclonal antibodies and the detection of a population of GPCMV and GPRV particles which expressed antigens of both viruses on their envelopes. Enhanced reverse transcriptase activity of GPRV and reduced infectivity titers of GPCMV was noted in dually infected cultures. These data suggest that interaction between GPCMV and GPRV had occurred in dually infected GPE cells and that expression of GPRV was enhanced.

摘要

对培养的豚鼠胚胎(GPE)细胞中巨细胞病毒和逆转录病毒的混合病毒感染进行了研究。含有5-溴-2'-脱氧尿苷和地塞米松的培养基可诱导培养的豚鼠细胞中内源性豚鼠逆转录病毒(GPRV)的表达。当诱导的GPE细胞被豚鼠巨细胞病毒(GPCMV)超感染时,观察到假型病毒颗粒。通过透射电子显微镜检查感染细胞的薄片,对两种病毒及其在感染细胞内的位置进行了形态学表征。使用5或15纳米大小的胶体金颗粒进行免疫标记,可使用GPCMV或GPRV特异性多克隆抗体鉴定每种病毒类型,并检测到一群在其包膜上表达两种病毒抗原的GPCMV和GPRV颗粒。在双重感染的培养物中,观察到GPRV的逆转录酶活性增强,GPCMV的感染性滴度降低。这些数据表明,在双重感染的GPE细胞中,GPCMV和GPRV之间发生了相互作用,并且GPRV的表达增强。

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