Literature DB >> 6314653

Defective interfering particles of Sendai virus modulate HN expression at the surface of infected BHK cells.

L Roux, F A Waldvogel.   

Abstract

The expression of the Sendai viral glycoproteins HN and F0 at the surface of BHK 21 cells was studied during infection with standard virus, with a mixture of standard and defective interfering (DI) particles (mixed virus infection), and during persistent infection. It is shown that by 2 days after infection, the expression of the HN protein at the surface of mixed virus-infected cells is reduced compared to that observed on standard virus-infected cells as estimated by cell surface immune precipitation of iodinated proteins. This reduced expression results from a reduced efficiency of HN insertion in the plasma membrane, as well as from the inaccessibility to antibody of part of the HN present at the membrane. The HN protein is also poorly expressed at the surface of persistently infected cells, originally infected with a mixture of DI and standard virus particles. In contrast, the expression of the F0 protein at the surface of the infected cells is similar regardless of the type of infection.

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Year:  1983        PMID: 6314653     DOI: 10.1016/0042-6822(83)90120-4

Source DB:  PubMed          Journal:  Virology        ISSN: 0042-6822            Impact factor:   3.616


  7 in total

1.  Characterization of human parainfluenza virus type 3 persistent infection in cell culture.

Authors:  A Moscona; M S Galinski
Journal:  J Virol       Date:  1990-07       Impact factor: 5.103

2.  Drastic immunoreactivity changes between the immature and mature forms of the Sendai virus HN and F0 glycoproteins.

Authors:  G Mottet; A Portner; L Roux
Journal:  J Virol       Date:  1986-07       Impact factor: 5.103

3.  Expression at the cell surface of biologically active fusion and hemagglutinin/neuraminidase proteins of the paramyxovirus simian virus 5 from cloned cDNA.

Authors:  R G Paterson; S W Hiebert; R A Lamb
Journal:  Proc Natl Acad Sci U S A       Date:  1985-11       Impact factor: 11.205

4.  Defective Viral Genomes Alter How Sendai Virus Interacts with Cellular Trafficking Machinery, Leading to Heterogeneity in the Production of Viral Particles among Infected Cells.

Authors:  Emmanuelle Genoyer; Carolina B López
Journal:  J Virol       Date:  2019-02-05       Impact factor: 5.103

5.  High-level eucaryotic in vivo expression of biologically active measles virus hemagglutinin by using an adenovirus type 5 helper-free vector system.

Authors:  G Alkhatib; D J Briedis
Journal:  J Virol       Date:  1988-08       Impact factor: 5.103

Review 6.  Defective Interfering Particles of Negative-Strand RNA Viruses.

Authors:  Christopher M Ziegler; Jason W Botten
Journal:  Trends Microbiol       Date:  2020-03-26       Impact factor: 17.079

7.  The Viral Polymerase Complex Mediates the Interaction of Viral Ribonucleoprotein Complexes with Recycling Endosomes during Sendai Virus Assembly.

Authors:  Emmanuelle Genoyer; Katarzyna Kulej; Chuan Tien Hung; Patricia A Thibault; Kristopher Azarm; Toru Takimoto; Benjamin A Garcia; Benhur Lee; Seema Lakdawala; Matthew D Weitzman; Carolina B López
Journal:  mBio       Date:  2020-08-25       Impact factor: 7.867

  7 in total

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