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Published July 1983 | public
Journal Article

Mutants of Sindbis Virus. IV. Heterotypic Complementation and Phenotypic Mixing between Temperature-sensitive Mutants and Wild-type Sindbis and Western Equine Encephalitis Viruses

Abstract

Heterotypic complementation between temperature-sensitive (ts) mutants of Sindbis (SIN) and Western equine encephalitis (WEE) viruses occurs under appropriate conditions. One heterotypic pair, SIN ts153 × WEE ts39 showed efficient complementation, and four other combinations gave detectable complementation, indicating that these two viruses, which are closely related serologically and biochemically, are sufficiently closely related to complement each other functionally. Cells mixedly infected with ts mutants or wild-type strains of both SIN and WEE viruses produced phenotypically mixed virions, in addition to both parental viruses. Various types of phenotypically mixed virions have been identified by neutralization with corresponding antisera, by thermal inactivation and by temperature sensitivity of replication. Some virions contained WEE genomes and envelopes containing primarily SIN proteins. Other phenotypically mixed virus yields contained primarily doubly neutralizable viruses which are presumed to have a mosaic of envelope proteins. Phenotypically mixed virions were morphologically indistinguishable from the parental types.

Additional Information

© 1983 Society for General Microbiology. Received: June 12 1982. Accepted: 3 March 1983 Published Online: Jan 07 1983. We would like to thank Dr A. Oya, Director of the Department of Virology and Rickettsiology and Dr James Strauss for their interest and encouragement in this joint project. We also wish to thank K. Suzuki for performing the electron microscopy and Mrs Edith Lenches for preparing stocks of the Sindbis mutants. This work was supported by grants GMO6965 and AI10793 and Biomedical Research Support grant 507RRO7003 from the National Institutes of Health and by grant PCM 80-22830 from the National Science Foundation.

Additional details

Created:
August 19, 2023
Modified:
October 18, 2023