Abstract
The replication of herpes simplex virus (HSV) was compared in rabbit and hamster cells at optimal and supraoptimal temperatures. Replication occurred in cells of either species at 33 C, but the total infectious virus yield was routinely about 10-fold greater in rabbit cells than in hamster cells. At 39 C, this difference was exaggerated to greater than 100,000-fold. Whereas infectious virus was produced and plaques formed in rabbit kidney cell monolayers at the higher temperature, neither developed in those derived from hamster embryos. Elevating the temperature from 33 C to 39 C at various time intervals after exposure of the cultures to virus revealed that production of infectious virus in hamster cells was completely heat-sensitive up to 6 hr after infection. Specific viral antigens and viral deoxyribonucleic acid (DNA) were synthesized in both rabbit and hamster cell cultures. In addition, cellular DNA synthesis was depressed and cytopathic effects occurred in both cell systems. These cytopathic effects were not observed in cell cultures treated with HSV previously inactivated with ultraviolet light. Compared with parallel cultures at 33 C, the amount of viral DNA synthesized at 39 C was greatly reduced in both systems. In hamster cells, the reduction was twofold greater than in rabbit cells. This cell-dependent thermal inhibition of HSV replication in hamster cells did not occur with vaccinia virus.
MeSH Terms
Animals
Antigens, Viral/analysis
Cells, Cultured/microbiology,radiation effects
Centrifugation, Density Gradient
Cricetinae/embryology
Cytopathogenic Effect, Viral
DNA/analysis,biosynthesis
DNA Replication
DNA, Viral/analysis,biosynthesis
Fluorescent Antibody Technique
Hot Temperature
Kidney
Rabbits
Radiation Effects
Simplexvirus/growth & development,immunology,radiation effects
Species Specificity
Temperature
Time Factors
Ultraviolet Rays
Virus Replication
Chemicals
Antigens, Viral
DNA, Viral
DNA
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Crouch N A
Rapp F
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