Literature DB >> 12560572

Stable expression of antisense RNAs targeted to the 5' non-coding region confers heterotypic inhibition to foot-and-mouth disease virus infection.

M F Rosas1,2, E Martínez-Salas2, F Sobrino1,2.   

Abstract

The antiviral potential of transcripts targeted to the non-coding regions (NCRs) of foot-and-mouth disease virus (FMDV) RNA have been studied during transient and constitutive expression in susceptible BHK-21 cells. Transient expression of antisense transcripts corresponding to the 5' and 3'NCRs, alone or in combination, confers specific inhibition of homologous (serotype C) virus infection in BHK-21 cells. Constitutive expression of antisense 5'NCR transcripts (5'AS) exerted higher levels of inhibition to homologous and heterologous (serotypes O, A, Asia, SAT 1, SAT 2 and SAT 3) FMDV infection, as estimated by a 10-fold reduction in virus titre in the supernatants from infected clones and by a plaque reduction assay. These inhibitions were also observed, albeit to a lesser extent, in clones stably expressing antisense 3'NCR transcripts. The antiviral response was specific for FMDV, as the picornavirus encephalomyocarditis virus was not inhibited in any of the transformed cell lines. In all cases, a correlation was found between the level of transcript expression and the extent of virus inhibition. The potential to efficiently inhibit FMDV, including isolates representing the seven serotypes, by expressing interfering 5'AS transcripts opens the possibility of developing transgenic animals with a reduced susceptibility to FMDV.

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Year:  2003        PMID: 12560572     DOI: 10.1099/vir.0.18668-0

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


  7 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.  A morpholino oligomer targeting highly conserved internal ribosome entry site sequence is able to inhibit multiple species of picornavirus.

Authors:  Jeffrey K Stone; Rene Rijnbrand; David A Stein; Yinghong Ma; Yan Yang; Patrick L Iversen; Raul Andino
Journal:  Antimicrob Agents Chemother       Date:  2008-03-17       Impact factor: 5.191

Review 3.  Insights into the biology of IRES elements through riboproteomic approaches.

Authors:  Almudena Pacheco; Encarnacion Martinez-Salas
Journal:  J Biomed Biotechnol       Date:  2010-02-02

4.  Inhibition of foot-and-mouth disease virus infections in cell cultures with antisense morpholino oligomers.

Authors:  Ariel Vagnozzi; David A Stein; Patrick L Iversen; Elizabeth Rieder
Journal:  J Virol       Date:  2007-08-29       Impact factor: 5.103

5.  Exploring IRES region accessibility by interference of foot-and-mouth disease virus infectivity.

Authors:  Teodoro Fajardo; Maria Flora Rosas; Francisco Sobrino; Encarnacion Martinez-Salas
Journal:  PLoS One       Date:  2012-07-18       Impact factor: 3.240

6.  Multiple microRNAs targeted to internal ribosome entry site against foot-and-mouth disease virus infection in vitro and in vivo.

Authors:  Yanyan Chang; Yongxi Dou; Huifang Bao; Xuenong Luo; Xuerong Liu; Kebin Mu; Zaixin Liu; Xiangtao Liu; Xuepeng Cai
Journal:  Virol J       Date:  2014-01-06       Impact factor: 4.099

7.  Disruption of Specific RNA-RNA Interactions in a Double-Stranded RNA Virus Inhibits Genome Packaging and Virus Infectivity.

Authors:  Teodoro Fajardo; Po-Yu Sung; Polly Roy
Journal:  PLoS Pathog       Date:  2015-12-08       Impact factor: 6.823

  7 in total

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