Cargando…
Improving initial infectivity of the Turnip mosaic virus (TuMV) infectious clone by an mini binary vector via agro-infiltration
BACKGROUND: The in vivo infectious clone of Turnip mosaic virus (TuMV), p35S-TuMV, was used on plant pathology research for many years. To activate p35S-TuMV, the plasmid was mechanically introduced to the local lesion host Chenopodium quinoa. However, low infectivity occurred when the TuMV from C....
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432745/ https://www.ncbi.nlm.nih.gov/pubmed/28510872 http://dx.doi.org/10.1186/1999-3110-54-22 |
_version_ | 1783236700705652736 |
---|---|
author | Lin, Yen-Yu Fang, Meng-Mei Lin, Pin-Chun Chiu, Ming-Tzu Liu, Li-Yu Lin, Chan-Pin Lin, Shih-Shun |
author_facet | Lin, Yen-Yu Fang, Meng-Mei Lin, Pin-Chun Chiu, Ming-Tzu Liu, Li-Yu Lin, Chan-Pin Lin, Shih-Shun |
author_sort | Lin, Yen-Yu |
collection | PubMed |
description | BACKGROUND: The in vivo infectious clone of Turnip mosaic virus (TuMV), p35S-TuMV, was used on plant pathology research for many years. To activate p35S-TuMV, the plasmid was mechanically introduced to the local lesion host Chenopodium quinoa. However, low infectivity occurred when the TuMV from C. quinoa was transferred to the systemic host Nicotiana benthamiana. RESULTS: To increase the efficiency of initial infectivity on N. benthamiana, the expression of the TuMV infectious clone by a binary vector that directly activates viral RNA through agro-infiltration is considered to be a good alternative. The size of the binary vector by agro-infiltration is usually large and its backbone has numerous restriction sites that increase difficulty for construction. In this study, we attempted to construct a mini binary vector (pBD003) with less restriction sites. The full-length cDNA of TuMV genome, with or without green fluorescence protein, was inserted in pBD003 to generate pBD-TuMV constructs, which were then individually introduced to N. benthamiana plants by agro-infiltration. Symptom development and ELISA positivity with TuMV antiserum indicated that the pBD-TuMV constructs are infectious. Moreover, the initial infectivity of a mild strain TuMV-GK, which contains an R(182)K mutation on HC-Pro, constructed in the pBD003 vector was significantly increased by agro-infiltration. CONCLUSION: Thus, we concluded that the newly constructed mini binary vector provides a more feasible tool for TuMV researches in areas, such as creating a mild strain for cross-protection, or a viral vector for foreign gene expression. In addition, the multiple cloning sites will be further cloned in pBD003 for convenience in constructing other viral infectious clones. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1999-3110-54-22) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5432745 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-54327452017-05-30 Improving initial infectivity of the Turnip mosaic virus (TuMV) infectious clone by an mini binary vector via agro-infiltration Lin, Yen-Yu Fang, Meng-Mei Lin, Pin-Chun Chiu, Ming-Tzu Liu, Li-Yu Lin, Chan-Pin Lin, Shih-Shun Bot Stud Research BACKGROUND: The in vivo infectious clone of Turnip mosaic virus (TuMV), p35S-TuMV, was used on plant pathology research for many years. To activate p35S-TuMV, the plasmid was mechanically introduced to the local lesion host Chenopodium quinoa. However, low infectivity occurred when the TuMV from C. quinoa was transferred to the systemic host Nicotiana benthamiana. RESULTS: To increase the efficiency of initial infectivity on N. benthamiana, the expression of the TuMV infectious clone by a binary vector that directly activates viral RNA through agro-infiltration is considered to be a good alternative. The size of the binary vector by agro-infiltration is usually large and its backbone has numerous restriction sites that increase difficulty for construction. In this study, we attempted to construct a mini binary vector (pBD003) with less restriction sites. The full-length cDNA of TuMV genome, with or without green fluorescence protein, was inserted in pBD003 to generate pBD-TuMV constructs, which were then individually introduced to N. benthamiana plants by agro-infiltration. Symptom development and ELISA positivity with TuMV antiserum indicated that the pBD-TuMV constructs are infectious. Moreover, the initial infectivity of a mild strain TuMV-GK, which contains an R(182)K mutation on HC-Pro, constructed in the pBD003 vector was significantly increased by agro-infiltration. CONCLUSION: Thus, we concluded that the newly constructed mini binary vector provides a more feasible tool for TuMV researches in areas, such as creating a mild strain for cross-protection, or a viral vector for foreign gene expression. In addition, the multiple cloning sites will be further cloned in pBD003 for convenience in constructing other viral infectious clones. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1999-3110-54-22) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2013-08-28 /pmc/articles/PMC5432745/ /pubmed/28510872 http://dx.doi.org/10.1186/1999-3110-54-22 Text en © Lin et al.; licensee Springer. 2013 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Lin, Yen-Yu Fang, Meng-Mei Lin, Pin-Chun Chiu, Ming-Tzu Liu, Li-Yu Lin, Chan-Pin Lin, Shih-Shun Improving initial infectivity of the Turnip mosaic virus (TuMV) infectious clone by an mini binary vector via agro-infiltration |
title | Improving initial infectivity of the Turnip mosaic virus (TuMV) infectious clone by an mini binary vector via agro-infiltration |
title_full | Improving initial infectivity of the Turnip mosaic virus (TuMV) infectious clone by an mini binary vector via agro-infiltration |
title_fullStr | Improving initial infectivity of the Turnip mosaic virus (TuMV) infectious clone by an mini binary vector via agro-infiltration |
title_full_unstemmed | Improving initial infectivity of the Turnip mosaic virus (TuMV) infectious clone by an mini binary vector via agro-infiltration |
title_short | Improving initial infectivity of the Turnip mosaic virus (TuMV) infectious clone by an mini binary vector via agro-infiltration |
title_sort | improving initial infectivity of the turnip mosaic virus (tumv) infectious clone by an mini binary vector via agro-infiltration |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432745/ https://www.ncbi.nlm.nih.gov/pubmed/28510872 http://dx.doi.org/10.1186/1999-3110-54-22 |
work_keys_str_mv | AT linyenyu improvinginitialinfectivityoftheturnipmosaicvirustumvinfectiousclonebyanminibinaryvectorviaagroinfiltration AT fangmengmei improvinginitialinfectivityoftheturnipmosaicvirustumvinfectiousclonebyanminibinaryvectorviaagroinfiltration AT linpinchun improvinginitialinfectivityoftheturnipmosaicvirustumvinfectiousclonebyanminibinaryvectorviaagroinfiltration AT chiumingtzu improvinginitialinfectivityoftheturnipmosaicvirustumvinfectiousclonebyanminibinaryvectorviaagroinfiltration AT liuliyu improvinginitialinfectivityoftheturnipmosaicvirustumvinfectiousclonebyanminibinaryvectorviaagroinfiltration AT linchanpin improvinginitialinfectivityoftheturnipmosaicvirustumvinfectiousclonebyanminibinaryvectorviaagroinfiltration AT linshihshun improvinginitialinfectivityoftheturnipmosaicvirustumvinfectiousclonebyanminibinaryvectorviaagroinfiltration |