Abstract
The prototype member of the complementation group II temperature-sensitive (ts) mutants of vesicular stomatitis virus, ts II 052, has been investigated. In ts II 052-infected HeLa cells at the restrictive temperature (39.5 degrees C), reduced viral RNA synthesis was observed by comparison with infections conducted at the permissive temperature (30 degrees C). It was found that for an infection conducted at 39.5 degrees C, no 38S RNA or intracytoplasmic nucleocapsids were present. For nucleocapsids isolated from ts II 052 purified virions or from ts II 052-infected cells at 30 degrees C, the RNA was sensitive to pancreatic RNase after an exposure at 39.5 degrees C in contrast to the resistance observed for wild-type virus. The nucleocapsid stability of wild-type virus when heated to 63 degrees C or submitted to varying pH was not found in nucleocapsids extracted from ts II 052 purified virions. The data suggest that for ts II 052 there is an altered relationship between the viral 38S RNA and the nucleocapsid protein(s) by comparison with wild-type virus. Such results argue for the complementation group II gene product being N protein, so that the ts defect in ts II 052 represents an altered N protein.
MeSH Terms
Genes
Genetic Complementation Test
HeLa Cells
Hydrogen-Ion Concentration
Mutation
RNA, Viral/biosynthesis
Temperature
Vesicular stomatitis Indiana virus/growth & development,metabolism
Viral Proteins/biosynthesis
Chemicals
RNA, Viral
Viral Proteins
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Combard A
Printz-Ane C
Martinet C
Printz P
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