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Strategies for the Construction of Cassava Brown Streak Disease Viral Infectious Clones
Cassava brown streak disease (CBSD) has major impacts on yield and quality of the tuberous roots of cassava in Eastern and Central Arica. At least two Potyviridae species cause the disease: Cassava brown streak virus (CBSV) and Ugandan cassava brown streak virus (UCBSV). Cloned viral genome sequence...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6513833/ https://www.ncbi.nlm.nih.gov/pubmed/30484144 http://dx.doi.org/10.1007/s12033-018-0139-7 |
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author | Duff-Farrier, C. R. A. Mbanzibwa, D. R. Nanyiti, S. Bunawan, H. Pablo-Rodriguez, J. L. Tomlinson, K. R. James, A. M. Alicai, T. Seal, S. E. Bailey, A. M. Foster, G. D. |
author_facet | Duff-Farrier, C. R. A. Mbanzibwa, D. R. Nanyiti, S. Bunawan, H. Pablo-Rodriguez, J. L. Tomlinson, K. R. James, A. M. Alicai, T. Seal, S. E. Bailey, A. M. Foster, G. D. |
author_sort | Duff-Farrier, C. R. A. |
collection | PubMed |
description | Cassava brown streak disease (CBSD) has major impacts on yield and quality of the tuberous roots of cassava in Eastern and Central Arica. At least two Potyviridae species cause the disease: Cassava brown streak virus (CBSV) and Ugandan cassava brown streak virus (UCBSV). Cloned viral genome sequences known as infectious clones (ICs) have been important in the study of other viruses, both as a means of standardising infectious material and characterising viral gene function. IC construction is often technically challenging for Potyviridae due to sequence instability in E. coli. Here, we evaluate three methods for the construction of infectious clones for CBSD. Whilst a simple IC for in vitro transcription was made for UCBSV isolate ‘Kikombe’, such an approach failed to deliver full-length clones for CBSV isolates ‘Nampula’ or ‘Tanza’, necessitating more complex approaches for their construction. The ICs successfully generated symptomatic infection in the model host N. benthamiana and in the natural host cassava. This shows that whilst generating ICs for CBSV is still a technical challenge, a structured approach, evaluating both in vitro and in planta transcription systems should successfully deliver ICs, allowing further study into the symptomology and virulence factors in this important disease complex. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12033-018-0139-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6513833 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-65138332019-05-28 Strategies for the Construction of Cassava Brown Streak Disease Viral Infectious Clones Duff-Farrier, C. R. A. Mbanzibwa, D. R. Nanyiti, S. Bunawan, H. Pablo-Rodriguez, J. L. Tomlinson, K. R. James, A. M. Alicai, T. Seal, S. E. Bailey, A. M. Foster, G. D. Mol Biotechnol Original Paper Cassava brown streak disease (CBSD) has major impacts on yield and quality of the tuberous roots of cassava in Eastern and Central Arica. At least two Potyviridae species cause the disease: Cassava brown streak virus (CBSV) and Ugandan cassava brown streak virus (UCBSV). Cloned viral genome sequences known as infectious clones (ICs) have been important in the study of other viruses, both as a means of standardising infectious material and characterising viral gene function. IC construction is often technically challenging for Potyviridae due to sequence instability in E. coli. Here, we evaluate three methods for the construction of infectious clones for CBSD. Whilst a simple IC for in vitro transcription was made for UCBSV isolate ‘Kikombe’, such an approach failed to deliver full-length clones for CBSV isolates ‘Nampula’ or ‘Tanza’, necessitating more complex approaches for their construction. The ICs successfully generated symptomatic infection in the model host N. benthamiana and in the natural host cassava. This shows that whilst generating ICs for CBSV is still a technical challenge, a structured approach, evaluating both in vitro and in planta transcription systems should successfully deliver ICs, allowing further study into the symptomology and virulence factors in this important disease complex. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12033-018-0139-7) contains supplementary material, which is available to authorized users. Springer US 2018-11-27 2019 /pmc/articles/PMC6513833/ /pubmed/30484144 http://dx.doi.org/10.1007/s12033-018-0139-7 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Paper Duff-Farrier, C. R. A. Mbanzibwa, D. R. Nanyiti, S. Bunawan, H. Pablo-Rodriguez, J. L. Tomlinson, K. R. James, A. M. Alicai, T. Seal, S. E. Bailey, A. M. Foster, G. D. Strategies for the Construction of Cassava Brown Streak Disease Viral Infectious Clones |
title | Strategies for the Construction of Cassava Brown Streak Disease Viral Infectious Clones |
title_full | Strategies for the Construction of Cassava Brown Streak Disease Viral Infectious Clones |
title_fullStr | Strategies for the Construction of Cassava Brown Streak Disease Viral Infectious Clones |
title_full_unstemmed | Strategies for the Construction of Cassava Brown Streak Disease Viral Infectious Clones |
title_short | Strategies for the Construction of Cassava Brown Streak Disease Viral Infectious Clones |
title_sort | strategies for the construction of cassava brown streak disease viral infectious clones |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6513833/ https://www.ncbi.nlm.nih.gov/pubmed/30484144 http://dx.doi.org/10.1007/s12033-018-0139-7 |
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