Literature DB >> 4101106

Defective virions of reovirus.

M Nonoyama, Y Watanabe, A F Graham.   

Abstract

When purified preparations of stock reovirus, type 3, were digested with chymotrypsin, the virions were converted into two different types of particle. These new particles could be separated from each other by isopycnic centrifugation in cesium chloride gradients. One particle banded at a buoyant density of 1.43 g/cm(3), the other at a density of 1.415 g/cm(3). The former particle is termed the heavy (H) particle, the latter is the light (L) particle. The ratio of H/L particles varied between 0.5 and 0.25 in various purified preparations of virus. In electron micrographs, both H and L particles had the appearance and dimensions of viral cores. H particles were infectious for L cells. When plaques formed by stock virus, or by H particles, were picked and propagated in L cells, the majority of the clones gave rise only to H particles on chymotrypsin digestion. On continued serial passage of the clones, virions containing L particles again appeared in the progeny. The simplest explanation of these results was that stock virus was comprised of two populations of virions. One type of virion which contained H particles was infectious, whereas the other, which contained L particles, was not itself infectious and could replicate only in cells coinfected with an H particle virion. Added weight was given to this hypothesis by two observations. First, a small but definite separation of H and L virions could be achieved by isopycnic centrifugation in a gradient of cesium chloride. Second, L particles and virions containing L particles were both shown to lack the largest of the ten segments of double-stranded ribonucleic acid genome. Thus, L particle virions have defective genomes.

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Year:  1970        PMID: 4101106      PMCID: PMC376112          DOI: 10.1128/JVI.6.2.226-236.1970

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  22 in total

1.  Specificity in transcription of the reovirus genome.

Authors:  Y Watanabe; L Prevec; A F Graham
Journal:  Proc Natl Acad Sci U S A       Date:  1967-09       Impact factor: 11.205

2.  The ribonucleic acids of the infective and interfering components of vesicular stomatitis virus.

Authors:  F Brown; S J Martin; B Cartwright; J Crick
Journal:  J Gen Virol       Date:  1967-10       Impact factor: 3.891

3.  Vesicular stomatitis virus RNA: complementarity between infected cell RNA and RNA's from infectious and autointerfering viral fractions.

Authors:  F L Schaffer; A J Hackett; M E Soergel
Journal:  Biochem Biophys Res Commun       Date:  1968-06-10       Impact factor: 3.575

4.  Defective T particles of vesicular stomatitis virus. I. Preparation, morphology, and some biologic properties.

Authors:  A S Huang; J W Greenawalt; R R Wagner
Journal:  Virology       Date:  1966-10       Impact factor: 3.616

5.  RNA polymerase activity in purified reoviruses.

Authors:  A J Shatkin; J D Sipe
Journal:  Proc Natl Acad Sci U S A       Date:  1968-12       Impact factor: 11.205

6.  Preparation and properties of the internal capsid components of reovirus.

Authors:  H D Mayor; L E Jordan
Journal:  J Gen Virol       Date:  1968-09       Impact factor: 3.891

7.  Polyacrylamide gel electrophoresis of influenza virus RNA.

Authors:  M W Pons; G K Hirst
Journal:  Virology       Date:  1968-02       Impact factor: 3.616

8.  Separation of ten reovirus genome segments by polyacrylamide gel electrophoresis.

Authors:  A J Shatkin; J D Sipe; P Loh
Journal:  J Virol       Date:  1968-10       Impact factor: 5.103

9.  Reovirus: RNA polymerase activity in purified virions.

Authors:  J Borsa; A F Graham
Journal:  Biochem Biophys Res Commun       Date:  1968-12-30       Impact factor: 3.575

10.  Resolution of multiple ribonucleic acid species by polyacrylamide gel electrophoresis.

Authors:  A C Peacock; C W Dingman
Journal:  Biochemistry       Date:  1967-06       Impact factor: 3.162

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  30 in total

1.  Control of transcription of the reovirus genome.

Authors:  M Nonoyama; S Millward; A F Graham
Journal:  Nucleic Acids Res       Date:  1974-03       Impact factor: 16.971

2.  Complementation between temperature-sensitive and deletion mutants of reovirus.

Authors:  D A Spandidos; A F Graham
Journal:  J Virol       Date:  1975-12       Impact factor: 5.103

3.  Complementation of defective reovirus by ts mutants.

Authors:  D A Spandidos; A F Graham
Journal:  J Virol       Date:  1975-04       Impact factor: 5.103

4.  Recombination between temperature-sensitive and deletion mutants of reovirus.

Authors:  D A Spandidos; A F Graham
Journal:  J Virol       Date:  1976-04       Impact factor: 5.103

5.  Regulated transcription of the genomes of defective virions and temperature-sensitive mutants of reovirus.

Authors:  D A Spandidos; G Krystal; A F Graham
Journal:  J Virol       Date:  1976-04       Impact factor: 5.103

6.  Persistent infections in L cells with temperature-sensitive mutants of reovirus.

Authors:  R Ahmed; A F Graham
Journal:  J Virol       Date:  1977-08       Impact factor: 5.103

7.  Quantitative characterization of defective virus emergence by deep sequencing.

Authors:  Collin Timm; Fulya Akpinar; John Yin
Journal:  J Virol       Date:  2013-12-18       Impact factor: 5.103

8.  Biochemical studies on bovine adenovirus type 3. II. Incomplete virus.

Authors:  K Igarashi; Y Niiyama; K Tsukamoto; T Kurokawa; Y Sugino
Journal:  J Virol       Date:  1975-09       Impact factor: 5.103

9.  Reovirus replicase-directed synthesis of double-stranded ribonucleic acid.

Authors:  S Sakuma; Y Watanabe
Journal:  J Virol       Date:  1972-10       Impact factor: 5.103

10.  Segment-specific inverted repeats found adjacent to conserved terminal sequences in wound tumor virus genome and defective interfering RNAs.

Authors:  J V Anzola; Z K Xu; T Asamizu; D L Nuss
Journal:  Proc Natl Acad Sci U S A       Date:  1987-12       Impact factor: 11.205

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