Affiliation:
1. Laboratories of Virology and Immunology, St. Jude Children's Research Hospital, and University of Tennessee Medical Units, Memphis, Tennessee 38101
Abstract
Ribonucleic acid (RNA) species in mumps virions and in infected cells were compared. The predominant RNA species in virions labeled with
3
H-uridine sedimented at 50
S
; RNA species sedimenting at 28, 18, and about 10
S
were also present. The virion-associated RNA species sedimenting slower than 50
S
contained some nucleotide sequences similar to 50
S
virion RNA. Although mumps virus replication was severely inhibited by high concentrations of actinomycin D, some virus was made, and virus-specific RNA species accumulated in infected cells. Mumps virus resembled other paramyxoviruses in inducing, in infected cells, synthesis not only of 50
S
RNA but also of slower sedimenting RNA species with a peak distribution at about 18
S
, complementary in base sequences to 50
S
virion RNA. In addition, base sequences of the parental type were relatively abundant in the RNA species sedimenting slower than 50
S
; these may represent precursors of the slowly sedimenting RNA species associated with virions. Ribonuclease-resistant RNA was detected in infected cells; this may represent replicative or transcriptive intermediates. Inhibition of protein synthesis with cycloheximide severely depressed accumulation of labeled 50
S
RNA in infected cells but did not interfere with accumulation of RNA species sedimenting slower than 50
S
. Actinomycin D treatment had a similar effect. Annealing of genomes and virus-induced complementary RNA species of Newcastle disease virus, Sendai virus, and mumps virus did not reveal any base sequence homologies.
Publisher
American Society for Microbiology
Subject
Virology,Insect Science,Immunology,Microbiology
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