Abstract
Cultures of Aedes albopictus cells persistently infected with wild-type Sindbis virus (SV-W) give rise to small plaque-forming mutants which are also temperature sensitive. These mutants, designated SV-C, are neutralized by antiserum produced against SV-W. Mutant ts clones were isolated from SV-C by plaque purification. After serial undiluted passage in BHK or mosquito cells, each of the clones gave rise to ts(+) revertants which, however, remained mutant with respect to plaque morphology. Nineteen of 20 clones derived from SV-C were RNA(+), and one was RNA(-) (SV-C-2). The RNA synthesizing activity, once induced in infected cells by SV-C-2, was stable at the nonpermissive temperature (39.5 C). All clones derived from SV-C were inactivated at 60 C much more quickly than was SV-W. It was not possible to demonstrate complementation between any of the SV-C clones.
MeSH Terms
Aedes
Animals
Antigens, Viral
Cell Line
Chick Embryo
Cricetinae
Culture Techniques
Dactinomycin/pharmacology
Genetic Complementation Test
Genetic Variation
Hemagglutination Tests
Kidney
Mutation
Neutralization Tests
Phenotype
RNA, Viral/biosynthesis
Sindbis Virus/growth & development,immunology,isolation & purification,metabolism
Temperature
Tritium
Uridine/metabolism
Viral Plaque Assay
Virus Cultivation
Chemicals
Antigens, Viral
RNA, Viral
Tritium
Dactinomycin
Uridine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Shenk T E
Koshelnyk K A
Stollar V
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