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PMID: 201154 Published · ppublish English Journal Article

Cytomegalovirus-induced membrane antigens in productively infected cells.

Acta microbiologica Academiae Scientiarum Hungaricae ·Vol. 24 ·No. 1 ·1977-00-00 ·Pages 21-8

Boldogh I, Gönczöl E, Váczi L

Abstract

Adsorbed but not penetrated virus can be removed from the CMV-infected cell membrane by digestion with cystine-activated papain. Membrane antigens appear on 80-90% of the infected cells 14-20 hr after infection as a result of de novo protein synthesis. Antigen synthesis can be blocked with inhibitors of protein synthesis, but not with DNA inhibitors. In the early stage of infection, pooled human convalescent serum reacted well with the membrane antigen, whereas pooled antiserum of rabbits immunized with CMV virion suspension gave a positive reaction with a small proportion of the cells. After the 48th hr, both the human and the rabbit serum pool reacted with the membrane of the infected cells. Absorption with cell cultured for 24 hr after CMV infection reduced the neutralization titres of the antisera only slightly but the titre reduction was considerable when absorption was performed with cells cultured for more than 48 hr after infection. It is concluded that on the membrane of cells productively infected by CMV at least two membrane antigens are present, one coded for by the DNA of the parent virus and another which is the product of the DNA of the virus progeny. The two antigens can be differentiated serologically.

MeSH Terms
Antigens, Viral/analysis Cell Membrane/immunology Cell Transformation, Viral Cells, Cultured Cytomegalovirus/immunology Time Factors Viral Proteins/biosynthesis,immunology
Chemicals
Antigens, Viral Viral Proteins
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Boldogh I
Gönczöl E
Váczi L
Article Info
Journal
Acta microbiologica Academiae Scientiarum Hungaricae
Abbr.
Acta Microbiol Acad Sci Hung
ISSN
0001-6187
Published
1977-00-00
Pages
21-8
Language
English
Region
Hungary
NLM ID
0370333
Subset
IM
External Links
PubMed source
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