Literature DB >> 6255069

Growth and release of several alphaviruses in chick and BHK cells.

E G Strauss, E M Lenches, M A Stamreich-Martin.   

Abstract

The growth and release of several alphaviruses, including several strains of Sindbis virus (the wild-type strain, the large plaque and small plaque variants of the HR strain, and the HR mutant ts103), Semliki Forest virus(SFV) and Middelburg virus, and of the unrelated rhabdovirus, vesicular stomatitis virus (VSV), have been compared in chick cells and in BHK-21 cells as a function of the culture conditions for the host cell and the ionic strength of the medium. The small plaque strain of Sindbis HR, as well as SFV, grew better in BHK cells, whereas the large plaque strain of Sindbis HR showed a preference for chick cells. Wild-type Sindbis and VSV grew equally well in either cell. The optimum ionic strength for virus production as well as inhibition of virus release into the medium at low ionic strength depended upon both the virus and the host cell. Thus, VSV grown in medium of low ionic strength gave no additional release of virus on incubation with hypertonic medium (minimum effect), whereas ts103 released very little virus without exposure to hypertonic conditions (maximum effect). The viruses could be ordered as follows: minimum effect = vesicular stomatitis virus < Middelburg virus < Semliki Forest virus < Sindbis wt < Sindbis HR (large plaque) < Sindbis HR (small plaque) < Sindbis ts103 = maximum effect. After several passages in culture, chick cells required hypertonic conditions for optimum production and release of Sindbis virus. Furthermore, BHK cells cultured in different media responded differently to ionic strength for virus production and release. These results suggest that there is a charge-dependent stop in the maturation of alpha-viruses, possibly a configurational rearrangement of glycoprotein E2 upon its formation from the precursor PE2, which is sensitive to the ionic strength of the medium, to the composition of the host plasmalemma and to differences in the virus glycoproteins.

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Year:  1980        PMID: 6255069     DOI: 10.1099/0022-1317-49-2-297

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


  6 in total

1.  Sindbis virus ts103 has a mutation in glycoprotein E2 that leads to defective assembly of virions.

Authors:  C S Hahn; C M Rice; E G Strauss; E M Lenches; J H Strauss
Journal:  J Virol       Date:  1989-08       Impact factor: 5.103

Review 2.  The alphaviruses: gene expression, replication, and evolution.

Authors:  J H Strauss; E G Strauss
Journal:  Microbiol Rev       Date:  1994-09

3.  Effects of anti-E2 monoclonal antibody on sindbis virus replication in AT3 cells expressing bcl-2.

Authors:  P Després; J W Griffin; D E Griffin
Journal:  J Virol       Date:  1995-11       Impact factor: 5.103

Review 4.  A structural and functional perspective of alphavirus replication and assembly.

Authors:  Joyce Jose; Jonathan E Snyder; Richard J Kuhn
Journal:  Future Microbiol       Date:  2009-09       Impact factor: 3.165

Review 5.  Alphavirus Replication: The Role of Cardiac Glycosides and Ion Concentration in Host Cells.

Authors:  Kauê F C Souza-Souza; Cassiano F Gonçalves-de-Albuquerque; Cláudio Cirne-Santos; Izabel C N P Paixão; Patrícia Burth
Journal:  Biomed Res Int       Date:  2020-05-09       Impact factor: 3.411

Review 6.  Na+/K+-ATPase as a Target of Cardiac Glycosides for the Treatment of SARS-CoV-2 Infection.

Authors:  Kauê Francisco Corrêa Souza E Souza; Bianca Portugal Tavares Moraes; Izabel Christina Nunes de Palmer Paixão; Patrícia Burth; Adriana Ribeiro Silva; Cassiano Felippe Gonçalves-de-Albuquerque
Journal:  Front Pharmacol       Date:  2021-04-15       Impact factor: 5.810

  6 in total

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