Abstract
A latent system employing measles virus (Schwarz strain) was developed in hamster embryo fibroblasts (HEF). Measles virus-specific antigen was detected by immunofluorescence in 30 to 50% of HEF cells, and these cells released infectious virus when co-cultivated with a susceptible monkey cell line, BSC-1 cells. No infectious virus could be detected in the cells when measures were taken to exclude passage of viable latent cells onto the indicator BSC-1 cells. Infectious center assays demonstrated that about 1 in 10 of the latently infected cells in the population could release infectious virus. Infectious virus appeared within 6 hr after co-cultivation of the HEF cells with BSC-1 cells, as compared to 24 hr required for normal replication of measles virus in the BSC-1 cells. Furthermore, labeling of progeny virus ribonucleic acid (RNA) by using tritiated uridine, and inhibition of RNA or protein synthesis by 5-azacytidine or cycloheximide suggested that neither additional RNA nor protein synthesis is required after co-cultivation of the cells to effect early virus release. It can therefore be postulated that there is a block at a late step in virus replication in the latently infected hamster cells. The most obvious site would concern maturation of infectious virions at the cell membrane.
MeSH Terms
Animals
Antigens, Viral/isolation & purification
Azacitidine/pharmacology
Cell Fusion
Cell Line
Cells, Cultured/immunology,microbiology
Cricetinae
Cycloheximide/pharmacology
Fibroblasts
Fluorescent Antibody Technique
Haplorhini
Kidney
Measles virus/growth & development,immunology,isolation & purification,metabolism
Neutralization Tests
Parainfluenza Virus 1, Human/growth & development
RNA, Viral/biosynthesis
Tritium
Uridine/metabolism
Viral Plaque Assay
Virus Replication
Chemicals
Antigens, Viral
RNA, Viral
Tritium
Cycloheximide
Azacitidine
Uridine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Knight P
Duff R
Rapp F
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17 references, click to expand
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