An efficient <it>Foxtail mosaic virus </it>vector system with reduced environmental risk

<p>Abstract</p> <p>Background</p> <p>Plant viral vectors offer high-yield expression of pharmaceutical and commercially important proteins with a minimum of cost and preparation time. The use of <it>Agrobacterium tumefaciens </it>has been introduced to deliv...

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Main Authors: Liu Zun, Kearney Christopher M
Format: Article
Language:English
Published: BMC 2010-12-01
Series:BMC Biotechnology
Online Access:http://www.biomedcentral.com/1472-6750/10/88
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spelling doaj-9199d0c43df24a27b7659e332c7f442e2020-11-25T03:55:11ZengBMCBMC Biotechnology1472-67502010-12-011018810.1186/1472-6750-10-88An efficient <it>Foxtail mosaic virus </it>vector system with reduced environmental riskLiu ZunKearney Christopher M<p>Abstract</p> <p>Background</p> <p>Plant viral vectors offer high-yield expression of pharmaceutical and commercially important proteins with a minimum of cost and preparation time. The use of <it>Agrobacterium tumefaciens </it>has been introduced to deliver the viral vector as a transgene to each plant cell via a simple, nonsterile infiltration technique called "agroinoculation". With agroinoculation, a full length, systemically moving virus is no longer necessary for excellent protein yield, since the viral transgene is transcribed and replicates in every infiltrated cell. Viral genes may therefore be deleted to decrease the potential for accidental spread and persistence of the viral vector in the environment.</p> <p>Results</p> <p>In this study, both the coat protein (CP) and triple gene block (TGB) genetic segments were eliminated from <it>Foxtail mosaic virus </it>to create the "FECT" vector series, comprising a deletion of 29% of the genome. This viral vector is highly crippled and expresses little or no marker gene within the inoculated leaf. However, when co-agroinoculated with a silencing suppressor (p19 or HcPro), FECT expressed GFP at 40% total soluble protein in the tobacco host, <it>Nicotiana benthamiana</it>. The modified FoMV vector retained the full-length replicase ORF, the TGB1 subgenomic RNA leader sequence and either 0, 22 or 40 bases of TGB1 ORF (in vectors FECT0, FECT22 and FECT40, respectively). As well as <it>N. benthamiana</it>, infection of legumes was demonstrated. Despite many attempts, expression of GFP via syringe agroinoculation of various grass species was very low, reflecting the low <it>Agrobacterium</it>-mediated transformation rate of monocots.</p> <p>Conclusions</p> <p>The FECT/40 vector expresses foreign genes at a very high level, and yet has a greatly reduced biohazard potential. It can form no virions and can effectively replicate only in a plant with suppressed silencing.</p> http://www.biomedcentral.com/1472-6750/10/88
collection DOAJ
language English
format Article
sources DOAJ
author Liu Zun
Kearney Christopher M
spellingShingle Liu Zun
Kearney Christopher M
An efficient <it>Foxtail mosaic virus </it>vector system with reduced environmental risk
BMC Biotechnology
author_facet Liu Zun
Kearney Christopher M
author_sort Liu Zun
title An efficient <it>Foxtail mosaic virus </it>vector system with reduced environmental risk
title_short An efficient <it>Foxtail mosaic virus </it>vector system with reduced environmental risk
title_full An efficient <it>Foxtail mosaic virus </it>vector system with reduced environmental risk
title_fullStr An efficient <it>Foxtail mosaic virus </it>vector system with reduced environmental risk
title_full_unstemmed An efficient <it>Foxtail mosaic virus </it>vector system with reduced environmental risk
title_sort efficient <it>foxtail mosaic virus </it>vector system with reduced environmental risk
publisher BMC
series BMC Biotechnology
issn 1472-6750
publishDate 2010-12-01
description <p>Abstract</p> <p>Background</p> <p>Plant viral vectors offer high-yield expression of pharmaceutical and commercially important proteins with a minimum of cost and preparation time. The use of <it>Agrobacterium tumefaciens </it>has been introduced to deliver the viral vector as a transgene to each plant cell via a simple, nonsterile infiltration technique called "agroinoculation". With agroinoculation, a full length, systemically moving virus is no longer necessary for excellent protein yield, since the viral transgene is transcribed and replicates in every infiltrated cell. Viral genes may therefore be deleted to decrease the potential for accidental spread and persistence of the viral vector in the environment.</p> <p>Results</p> <p>In this study, both the coat protein (CP) and triple gene block (TGB) genetic segments were eliminated from <it>Foxtail mosaic virus </it>to create the "FECT" vector series, comprising a deletion of 29% of the genome. This viral vector is highly crippled and expresses little or no marker gene within the inoculated leaf. However, when co-agroinoculated with a silencing suppressor (p19 or HcPro), FECT expressed GFP at 40% total soluble protein in the tobacco host, <it>Nicotiana benthamiana</it>. The modified FoMV vector retained the full-length replicase ORF, the TGB1 subgenomic RNA leader sequence and either 0, 22 or 40 bases of TGB1 ORF (in vectors FECT0, FECT22 and FECT40, respectively). As well as <it>N. benthamiana</it>, infection of legumes was demonstrated. Despite many attempts, expression of GFP via syringe agroinoculation of various grass species was very low, reflecting the low <it>Agrobacterium</it>-mediated transformation rate of monocots.</p> <p>Conclusions</p> <p>The FECT/40 vector expresses foreign genes at a very high level, and yet has a greatly reduced biohazard potential. It can form no virions and can effectively replicate only in a plant with suppressed silencing.</p>
url http://www.biomedcentral.com/1472-6750/10/88
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