Literature DB >> 6251785

Electron microscope study of cultured cells of the chorioallantoic membrane infected with representative paramyxoviruses.

J T Seto, K Wahn, H Becht.   

Abstract

Chorioallantoic membrane (CAM) tissue cultures were found to be permissive for representative paramyxoviruses. The CAM cells can be used for plaque assay without the presence of trypsin. Ultrastructures of CAM cells infected with paramyxovirus Yucaipa (PMY), Sendai virus, and NDV were different. Nucleocapsids were readily seen in budding structures of cells infected with PMY, and in Sendai virus infected cells, large clusters of nucleocapsids were clearly evident in the cytoplasm. The site of glycoprotein cleavage does not have any effect on the nature of budding. It appears that a factor or factors in addition to the nature of the plasma membrane influences the morphology of cells infected with paramyxoviruses.

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Year:  1980        PMID: 6251785     DOI: 10.1007/bf01314541

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


  14 in total

1.  Intracellular metabolism of sendai virus nucleocapside.

Authors:  D W Kingsbury; C H Hsu; K G Murti
Journal:  Virology       Date:  1978-11       Impact factor: 3.616

2.  The synthesis of sendai virus polypeptides in infected cells.

Authors:  R A Lamb; B W Mahy; P W Choppin
Journal:  Virology       Date:  1976-01       Impact factor: 3.616

3.  Studies on the assembly of the envelope of Newcastle disease virus.

Authors:  Y Nagai; H Ogura; H Klenk
Journal:  Virology       Date:  1976-02       Impact factor: 3.616

4.  Proteolytic cleavage of the viral glycoproteins and its significance for the virulence of Newcastle disease virus.

Authors:  Y Nagai; H D Klenk; R Rott
Journal:  Virology       Date:  1976-07-15       Impact factor: 3.616

5.  Identification of biological activities of paramyxovirus glycoproteins. Activation of cell fusion, hemolysis, and infectivity of proteolytic cleavage of an inactive precursor protein of Sendai virus.

Authors:  A Scheid; P W Choppin
Journal:  Virology       Date:  1974-02       Impact factor: 3.616

6.  Trypsin action on the growth of Sendai virus in tissue culture cells. 3. Structural difference of Sendai viruses grown in eggs and tissue culture cells.

Authors:  M Homma; M Ouchi
Journal:  J Virol       Date:  1973-12       Impact factor: 5.103

7.  The spread of a pathogenic and an apathogenic strain of Newcastle disease virus in the chick embryo as depending on the protease sensitivity of the virus glycoproteins.

Authors:  Y Nagai; K Shimokata; T Yoshida; M Hamaguchi; M Iinuma; K Maeno; T Matsumoto; H D Klenk; R Rott
Journal:  J Gen Virol       Date:  1979-11       Impact factor: 3.891

8.  An electron microscopic study of moderate and virulent virus-cell interactions of the parainfluenza virus SV5.

Authors:  R W Compans; K V Holmes; S Dales; P W Choppin
Journal:  Virology       Date:  1966-11       Impact factor: 3.616

9.  Ortho- and paramyxoviruses from migrating feral ducks: characterization of a new group of influenza A viruses.

Authors:  R G Webster; M Morita; C Pridgen; B Tumova
Journal:  J Gen Virol       Date:  1976-08       Impact factor: 3.891

10.  Newcastle disease virus infection of L cells.

Authors:  T T Hecht; D F Summers
Journal:  J Virol       Date:  1974-07       Impact factor: 5.103

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  2 in total

1.  Persistent infections with Sendai virus and Newcastle disease viruses.

Authors:  P Lawton; Z Karimi; L Mancinelli; J T Seto
Journal:  Arch Virol       Date:  1986       Impact factor: 2.574

2.  The site of cleavage in infected cells and polypeptides of representative paramyxoviruses grown in cultured cells of the chorioallantoic membrane.

Authors:  J T Seto; W Garten; R Rott
Journal:  Arch Virol       Date:  1981       Impact factor: 2.574

  2 in total

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