Literature DB >> 1239990

Electron microscopical study of initial and final stages of fowl plague virus-replication in chick embryo cells.

M Reinacher, E Weiss.   

Abstract

Cellular uptake of fowl plague virus occurs 10-30 minutes after inoculation of chick embryo cells. The penetration of the virions is by pinocytosis (viropexis); fusion with the cellular membrane has not been observed. After pinocytosis the virions become gradually disintegrated. Budding of newly formed virions from the cellular membrane starts 3 hours post inoculation (p.i.) and reaches its maximum 8 hours p.i. At the same time budding takes place into electron microscopically empty and autophagic vacuoles. Eight hours p.i. about 3 per cent of the infected cells show budding of virions from the surface and into cytoplasmic vacuoles. Labelling of the cellular membrane with ruthenium red demonstrated that these cytoplasmic vacuoles are not simple cross-sections of invaginations of the cellular membrane. Cluster-like structures were found at 6 hours p.i. in the nuclei of infected cells; however, the suggestion that the clusters develop from nucleoli could not be confirmed.

Entities:  

Mesh:

Year:  1975        PMID: 1239990     DOI: 10.1007/bf01317537

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


  23 in total

1.  The entry of myxoviruses into the cell.

Authors:  L HOYLE
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1962

2.  Ultrastructural localization of influenza virus antigens in infected chick embryo cells as revealed by a peroxidase-labelled antibody method.

Authors:  F Ciampor; M Bystrická; J Rajcáni
Journal:  Arch Gesamte Virusforsch       Date:  1974

3.  Infection of chick embryo tracheal organ cultures with influenza A2 (Hong Kong) virus. II. Electron microscopy.

Authors:  P Blaskovic; A J Rhodes; F W Doane; N A Labzoffsky
Journal:  Arch Gesamte Virusforsch       Date:  1972

4.  [Ultrastructural equivalents of cellular autophagy. Electronmicroscopy observations on spermatids of Eisenia foetida during the cytoplasmic reduction].

Authors:  C Stang-Voss
Journal:  Z Zellforsch Mikrosk Anat       Date:  1972

5.  Ruthenium red and violet. I. Chemistry, purification, methods of use for electron microscopy and mechanism of action.

Authors:  J H Luft
Journal:  Anat Rec       Date:  1971-11

6.  An electron microscopic study of single-cycle infection of chick embryo fibroblasts by influenza virus.

Authors:  R W Compans; N J Dimmock
Journal:  Virology       Date:  1969-11       Impact factor: 3.616

7.  Penetration of nuclear inclusions into the cytoplasm in influenze-virus-infected cells.

Authors:  E Anisimová; E Tucková; V Vonka
Journal:  Intervirology       Date:  1974       Impact factor: 1.763

Review 8.  Early events in cell-animal virus interactions.

Authors:  S Dales
Journal:  Bacteriol Rev       Date:  1973-06

9.  Procedure for embedding in situ selected cells cultured in vitro.

Authors:  B R Brinkley; P Murphy; L C Richardson
Journal:  J Cell Biol       Date:  1967-10       Impact factor: 10.539

10.  THE APPLICATION OF FERRITIN-CONJUGATED ANTIBODY TO ELECTRON MICROSCOPIC STUDIES OF INFLUENZA VIRUS IN INFECTED CELLS : I. THE CELLULAR SURFACE.

Authors:  C Morgan; K C Hsu; R A Rifkind; A W Knox; H M Rose
Journal:  J Exp Med       Date:  1961-10-31       Impact factor: 14.307

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