Literature DB >> 1848750

Characterization of fusion from without induced by herpes simplex virus.

I Walev1, K C Wollert, K Weise, D Falke.   

Abstract

The process of fusion from without (FFWO) induced by herpes simplex virus (HSV) was analyzed by using various inhibitors and compared to fusion from within (FFWI). The fate of certain elements of the cytoskeleton after FFWO was also investigated. Our experiments demonstrate FFWO as a very suitable system for study of early virus-cell interactions. Zn++ ions proved inhibitory for penetration whilst pretreatment of cells with Ca++ ions before infection enhanced FFWO activity. Dissociation of penetration from the fusion process itself was possible by use of Zn++ ions, low pH-treatment and antiserum on the one hand and N-ethylmaleimide and cytochalasin D on the other. Penetration itself needs only 6 min or less to proceed. FFWO is independent of inhibitors of glycosylation (tunicamycin) and intracellular vesicular traffic (monensin), protein-synthesis (cycloheximide) and energy-delivery (2.4 dinitrophenol and Na-azide). Analyzed strains of HSV-1 and -2 producing FFWI could be subgrouped into three categories: Strain ANG with high, strain HFEM and Lux with low and strains IES, Len, MP, US with no FFWO activity. The results of these experiments indicate that the property of FFWO is not purely a consequence of the number of PFU but depends on certain inherent properties of the virus particles. Addition of heparin as well as treatment of cells with heparitinase effectively prevented FFWO, indicating identical virus receptors for entrance of virus into cells and FFWO. During our studies several calf sera were found to inhibit FFWO-activity. Inhibition of FFWO by a glycoconjugate (ferritin coupled with oleic acid) indicates specific stereochemical hindrance of FFWO by this compound. Shortly after FFWO the actin filaments rearrange to form long fibres and surface fibronectin is being lost from the cell membrane.

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Year:  1991        PMID: 1848750     DOI: 10.1007/bf01310490

Source DB:  PubMed          Journal:  Arch Virol        ISSN: 0304-8608            Impact factor:   2.574


  30 in total

1.  Inhibition of herpes simplex virus type 1 penetration by cytochalasins B and D.

Authors:  K S Rosenthal; R Perez; C Hodnichak
Journal:  J Gen Virol       Date:  1985-07       Impact factor: 3.891

2.  Herpes simplex virus glycoproteins associated with different morphological entities projecting from the virion envelope.

Authors:  L M Stannard; A O Fuller; P G Spear
Journal:  J Gen Virol       Date:  1987-03       Impact factor: 3.891

3.  [Ca++, histidine, and Zn++ as factors in the formation of giant cells by herpesivirus hominis].

Authors:  D Falke
Journal:  Z Med Mikrobiol Immunol       Date:  1967

4.  Identification of herpes simplex virus type 1 glycoproteins interacting with the cell surface.

Authors:  J E Kühn; M D Kramer; W Willenbacher; U Wieland; E U Lorentzen; R W Braun
Journal:  J Virol       Date:  1990-06       Impact factor: 5.103

5.  A role for herpes simplex virus type 1 glycoprotein E in induction of cell fusion.

Authors:  S Chatterjee; J Koga; R J Whitley
Journal:  J Gen Virol       Date:  1989-08       Impact factor: 3.891

6.  Ammonium chloride inhibits cell fusion induced by syn mutants of herpes simplex virus type 1.

Authors:  T C Holland; S Person
Journal:  J Virol       Date:  1977-07       Impact factor: 5.103

7.  Rat myoblast fusion requires metalloendoprotease activity.

Authors:  C B Couch; W J Strittmatter
Journal:  Cell       Date:  1983-01       Impact factor: 41.582

8.  A fusion protein required for vesicle-mediated transport in both mammalian cells and yeast.

Authors:  D W Wilson; C A Wilcox; G C Flynn; E Chen; W J Kuang; W J Henzel; M R Block; A Ullrich; J E Rothman
Journal:  Nature       Date:  1989-06-01       Impact factor: 49.962

9.  Biochemical studies on cell fusion. I. Lipid composition of fusion-resistant cells.

Authors:  D S Roos; P W Choppin
Journal:  J Cell Biol       Date:  1985-10       Impact factor: 10.539

10.  Biochemical studies on cell fusion. II. Control of fusion response by lipid alteration.

Authors:  D S Roos; P W Choppin
Journal:  J Cell Biol       Date:  1985-10       Impact factor: 10.539

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  6 in total

1.  Relationship between HLA I surface expression and different cytopathic effects produced after herpes simplex virus infection in vitro.

Authors:  I Walev; J Kunkel; W Schwaeble; K Weise; D Falke
Journal:  Arch Virol       Date:  1992       Impact factor: 2.574

2.  Two mutations in gB-1 and gD-1 of herpes simplex virus type 1 are involved in the "fusion from without" phenotype in different cell types.

Authors:  M Lingen; T Seck; K Weise; D Falke
Journal:  Virus Genes       Date:  1996       Impact factor: 2.332

3.  The nectin-1alpha transmembrane domain, but not the cytoplasmic tail, influences cell fusion induced by HSV-1 glycoproteins.

Authors:  Ravi P Subramanian; Jennifer E Dunn; Robert J Geraghty
Journal:  Virology       Date:  2005-09-01       Impact factor: 3.616

4.  Evidence for a multistep mechanism for cell-cell fusion by herpes simplex virus with mutations in the syn 3 locus using heparin derivatives during fusion from within.

Authors:  T Seck; M Lingen; K Weise; D Falke
Journal:  Arch Virol       Date:  1994       Impact factor: 2.574

5.  Cyclosporin A resistance of herpes simplex virus-induced "fusion from within" as a phenotypical marker of mutations in the Syn 3 locus of the glycoprotein B gene.

Authors:  I Walev; M Lingen; M Lazzaro; K Weise; D Falke
Journal:  Virus Genes       Date:  1994-01       Impact factor: 2.332

6.  Nectin-2-mediated entry of a syncytial strain of herpes simplex virus via pH-independent fusion with the plasma membrane of Chinese hamster ovary cells.

Authors:  Mark G Delboy; Jennifer L Patterson; Aimee M Hollander; Anthony V Nicola
Journal:  Virol J       Date:  2006-12-27       Impact factor: 4.099

  6 in total

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