Genetic exclusion and stable complementation of Sindbis virus
- 1 September 1976
- journal article
- research article
- Published by Springer Nature in Archiv für die gesamte Virusforschung
- Vol. 50 (3) , 177-187
- https://doi.org/10.1007/bf01320571
Abstract
In an effort to enhance genetic interactions by eliminating spatial or physical barriers between variants of Sindbis virus, MgCl2 was used to aggregate infecting viral particles. Mixing viral samples in a 1:1 ratio with 0.5m MgCl2 produced maximal reduction in plaque forming units (PFU) with minimal cell damage due to MgCl2. Aggregate size was determined to be about 7 PFU. Samples taken at 3, 5 and 10 hours after infection with mixed aggregates composed of large and small plaque forming virus indicated that only one type of genome was represented among the progeny particles. In addition, aggregation enhanced complementation and the progeny were stable after several cycles of sonication and passage.This publication has 18 references indexed in Scilit:
- Mechanism of Sindbis Virus-Induced Intrinsic Interference with Vesicular Stomatitis Virus ReplicationJournal of Virology, 1974
- Genome of Sindbis virus.1972
- The process of infection with bacteriophage phiX174. 8. Evidence for an essential bacterial "site".1967
- Electrophoretic Evidence for a Single Protein Component in the Capsid of Polyoma VirusJournal of General Virology, 1967
- Complementation between temperature-sensitive mutants of Sindbis virusVirology, 1966
- Isolation and characterization of conditional-lethal mutants of Sindbis virusVirology, 1966
- Studies on mixed infection with Newcastle disease virusVirology, 1959
- Homotypic Non-exclusion by Vesicular Stomatitis Virus in Chick Cell CultureJournal of General Microbiology, 1958
- Sindbis Virus: A Newly Recognized Arthropod-Transmitted VirusThe American Journal of Tropical Medicine and Hygiene, 1955
- Production of Plaques in Monolayer Tissue Cultures by Single Particles of an Animal VirusProceedings of the National Academy of Sciences, 1952