Abstract
Accumulation of the nucleoprotein of vesicular stomatitis virus (VSV) in the cytoplasm of BHK-21 cells and in two of four human cell lines was demonstrated. Appearance and progression of the nucleoprotein inclusions paralleled development of virus-specific immunofluorescence and production of virus progeny. The inclusions appeared early as discrete foci of filamentous material which eventually increased in size to form large masses which replaced normal cytoplasmic constituents. The filamentous strands were found in close proximity to budding virions. The inclusion material was extracted from infected cells and purified in cesium chloride gradients. The isolated filaments resembled the ribonucleoprotein isolated from purified virions. They incorporated (3)H-uridine, exhibited virus-specific complement-fixing activity, had a buoyant density of 1.32 g/cm(3), and appeared as single wavy strands the width of which varied from 2.5 to 8.5 nm, depending on the angle of viewing.
MeSH Terms
Amnion
Animals
Cell Line
Cell Membrane/microbiology
Centrifugation, Density Gradient
Cesium
Chlorides
Complement Fixation Tests
Cricetinae
Culture Techniques
Cytoplasm/microbiology
Fibroblasts
Fluorescent Antibody Technique
Humans
Immune Sera
Inclusion Bodies, Viral
Kidney
Lymphocytes
Male
Microscopy, Electron
Nucleoproteins/analysis,metabolism
Penis
Rabbits
Spectrophotometry
Staining and Labeling
Tritium
Uridine/metabolism
Vesicular stomatitis Indiana virus/growth & development,immunology,metabolism,pathogenicity
Viral Proteins/analysis,metabolism
Virus Replication
Chemicals
Chlorides
Immune Sera
Nucleoproteins
Viral Proteins
Tritium
Cesium
Uridine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Zajac B A
Hummeler K
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