Literature DB >> 10773736

Hepatitis A virus replication: an intermediate in the uncoating process.

N E Bishop1.   

Abstract

Dense, RNase-sensitive, VP2-containing, non-infectious hepatitis A virus (HAV) particles were found to be formed at early times after the infection of cultured cells. These particles formed with kinetics mirroring those reported for HAV uncoating. The kinetics of the formation of dense HAV particles corresponded to a decrease in detectable, mature input virions, as detected by RNA dot blot hybridization of CsCl density gradient fractions. The dense HAV particles did not appear to have altered sedimentation coefficients, and as the fate of small capsid protein VP4 is not yet known, these particles cannot yet be termed 'A particles' or 'infectosomes', as have the uncoating intermediates in some picornavirus-cell systems. Copyright 2000 S. Karger AG, Basel.

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Year:  2000        PMID: 10773736     DOI: 10.1159/000025021

Source DB:  PubMed          Journal:  Intervirology        ISSN: 0300-5526            Impact factor:   1.763


  3 in total

1.  Alteration of hepatitis A virus (HAV) particles by a soluble form of HAV cellular receptor 1 containing the immunoglobin-and mucin-like regions.

Authors:  Erica Silberstein; Li Xing; Willem van de Beek; Jinhua Lu; Holland Cheng; Gerardo G Kaplan
Journal:  J Virol       Date:  2003-08       Impact factor: 5.103

2.  Changes to lipid droplet configuration in mCMV-infected fibroblasts: live cell imaging with simultaneous CARS and two-photon fluorescence microscopy.

Authors:  Christine S Y Wong; Iain Robinson; Michael A Ochsenkühn; Jochen Arlt; William J Hossack; Jason Crain
Journal:  Biomed Opt Express       Date:  2011-08-02       Impact factor: 3.732

Review 3.  Molecular biology and inhibitors of hepatitis A virus.

Authors:  Yannick Debing; Johan Neyts; Hendrik Jan Thibaut
Journal:  Med Res Rev       Date:  2013-05-30       Impact factor: 12.944

  3 in total

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