Literature DB >> 2998059

Early steps in FMDV replication: further analysis on the effects of chloroquine.

E C Carrillo, C Giachetti, R Campos.   

Abstract

We have previously demonstrated that chloroquine and NH4Cl, two well-known lysosomotropic drugs inhibit foot-and-mouth disease virus (FMDV) replication. This fact points to the relevance of an acidic environment during FMDV penetration. In the present report, we show that chloroquine prevents the cell-mediated disruption of 140 S virions into 12 S particles. This dissociation, which resembles that caused by low pH in vitro, might be an initial uncoating step. Furthermore, we demonstrated that a decrease in the environmental pH counteracts the effect of chloroquine indicating that viral disruption is a low-pH cell-mediated process. The fact that it still occurs at low temperature (20 degrees) and shortly after viral adsorption suggests not only that prelysosomal vesicles represent the putative site for uncoating but also cause the virion to uncoat.

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Year:  1985        PMID: 2998059     DOI: 10.1016/0042-6822(85)90232-6

Source DB:  PubMed          Journal:  Virology        ISSN: 0042-6822            Impact factor:   3.616


  14 in total

Review 1.  Foot-and-mouth disease.

Authors:  Marvin J Grubman; Barry Baxt
Journal:  Clin Microbiol Rev       Date:  2004-04       Impact factor: 26.132

2.  The effect of lipophilic amines on the growth of hepatitis A virus in Frp/3 cells.

Authors:  F Superti; L Seganti; N Orsi; M Divizia; R Gabrieli; A Panà
Journal:  Arch Virol       Date:  1987       Impact factor: 2.574

3.  Analysis of foot-and-mouth disease virus internalization events in cultured cells.

Authors:  Vivian O'Donnell; Michael LaRocco; Hernando Duque; Barry Baxt
Journal:  J Virol       Date:  2005-07       Impact factor: 5.103

4.  Entry of poliovirus into cells does not require a low-pH step.

Authors:  L Pérez; L Carrasco
Journal:  J Virol       Date:  1993-08       Impact factor: 5.103

5.  A single amino acid substitution in the capsid of foot-and-mouth disease virus can increase acid resistance.

Authors:  Miguel A Martín-Acebes; Angela Vázquez-Calvo; Verónica Rincón; Mauricio G Mateu; Francisco Sobrino
Journal:  J Virol       Date:  2010-12-22       Impact factor: 5.103

6.  Characterization of synthetic foot-and-mouth disease virus provirions separates acid-mediated disassembly from infectivity.

Authors:  T Knipe; E Rieder; B Baxt; G Ward; P W Mason
Journal:  J Virol       Date:  1997-04       Impact factor: 5.103

7.  A single amino acid substitution in the capsid of foot-and-mouth disease virus can increase acid lability and confer resistance to acid-dependent uncoating inhibition.

Authors:  Miguel A Martín-Acebes; Verónica Rincón; Rosario Armas-Portela; Mauricio G Mateu; Francisco Sobrino
Journal:  J Virol       Date:  2010-01-06       Impact factor: 5.103

8.  Viral RNA modulates the acid sensitivity of foot-and-mouth disease virus capsids.

Authors:  S Curry; C C Abrams; E Fry; J C Crowther; G J Belsham; D I Stuart; A M King
Journal:  J Virol       Date:  1995-01       Impact factor: 5.103

9.  Establishment of persistent infection with foot-and-mouth disease virus in BHK-21 cells.

Authors:  Xuan Huang; Yong Li; Hui Fang; Congyi Zheng
Journal:  Virol J       Date:  2011-04-14       Impact factor: 4.099

Review 10.  Recycling of chloroquine and its hydroxyl analogue to face bacterial, fungal and viral infections in the 21st century.

Authors:  Jean-Marc Rolain; Philippe Colson; Didier Raoult
Journal:  Int J Antimicrob Agents       Date:  2007-07-16       Impact factor: 5.283

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