Literature DB >> 932694

Defective-interfering particles of Semliki Forest Virus: structural differences between standard virus and defective-interfering particles.

C J Bruton, S I Kennedy.   

Abstract

Serial passaging of Semlike Forest virus in BHK cells at a constant input multiplicity of 50 p.f.u./cell resulted in a 4 log10 drop in yield of infectious virus by passage 9. An interference analysis showed that this drop was due to the presence of defective-interfering (DI) particles. Attempts were made to separate the DI particles from standard virus by equilibrium and velocity centrifugation. Only equilbrium centrifugation on CsCl resolved the DI particles (identified by interference analyses) from standard virus. The buoyant density of the DI particles (1.23 g/ml) was higher than that of standard virus (p = 1-20 g/ml). No difference was observed between the structural porteins of standard virus and DI particles. Analysis of the RNA of standard virus and DI particles showed that whereas standard virus contained only 42S RNA (mol. wt. approx. 4-2 X 10(6), DI particles contained two small pieces of RNA of mol. wt. 0.81 and 0-75 X 10(6) respectively. Infectivity assays showed that these low mol. wt. species were not only non-infectious but also interfered with the infectivity of 42S RNA from standard virus. Nucleocapsids derived from purified DI particles had a buoyant density 0-02 g/ml greater than the nucleocapsids from standard virus. Analysis of the RNA from DI nucleocapsids showed it to be entirely of the low mol. wt. class. To account therefore for the density difference not only between DI particles and standard virus but also between their respective nucleocapsids we propose that each SFV DI particle contains several molecules of the low mol. wt. RNA species.

Entities:  

Mesh:

Substances:

Year:  1976        PMID: 932694     DOI: 10.1099/0022-1317-31-3-383

Source DB:  PubMed          Journal:  J Gen Virol        ISSN: 0022-1317            Impact factor:   3.891


  19 in total

1.  Persistent infection of cultured mammalian cells by Japanese encephalitis virus.

Authors:  C Schmaljohn; C D Blair
Journal:  J Virol       Date:  1977-11       Impact factor: 5.103

Review 2.  The mode of assembly of alphavirus cores implies a mechanism for the disassembly of the cores in the early stages of infection. Brief review.

Authors:  G Wengler
Journal:  Arch Virol       Date:  1987       Impact factor: 2.574

3.  Structural complexity of defective-interfering RNAs of Semliki Forest virus as revealed by analysis of complementary DNA.

Authors:  H Söderlund; S Keränen; P Lehtovaara; I Palva; R F Pettersson; L Kääriäinen
Journal:  Nucleic Acids Res       Date:  1981-07-24       Impact factor: 16.971

4.  Replication of standard and defective Ross River virus in BHK cells: patterns of viral RNA and polypeptide synthesis.

Authors:  J H Martin; R C Weir; L Dalgarno
Journal:  Arch Virol       Date:  1979       Impact factor: 2.574

5.  Bovine viral diarrhea virus: characterization of a cytopathogenic defective interfering particle with two internal deletions.

Authors:  H Kupfermann; H J Thiel; E J Dubovi; G Meyers
Journal:  J Virol       Date:  1996-11       Impact factor: 5.103

6.  Synthesis of alphavirus-specified RNA.

Authors:  H Brzeski; S I Kennedy
Journal:  J Virol       Date:  1978-02       Impact factor: 5.103

7.  Coronavirus multiplication strategy. I. Identification and characterization of virus-specified RNA.

Authors:  D F Stern; S I Kennedy
Journal:  J Virol       Date:  1980-06       Impact factor: 5.103

8.  Semliki Forest virus multiplication in clones of Aedes albopictus cells.

Authors:  P Tooker; S I Kennedy
Journal:  J Virol       Date:  1981-02       Impact factor: 5.103

9.  Defective interfering particles of mouse hepatitis virus.

Authors:  S Makino; F Taguchi; K Fujiwara
Journal:  Virology       Date:  1984-02       Impact factor: 3.616

10.  Defective interfering passages of Sindbis virus: nature of the defective virion RNA.

Authors:  S I Kennedy; C J Bruton; B Weiss; S Schlesinger
Journal:  J Virol       Date:  1976-09       Impact factor: 5.103

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.