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Cassava brown streak virus has a rapidly evolving genome: implications for virus speciation, variability, diagnosis and host resistance
Cassava is a major staple food for about 800 million people in the tropics and sub-tropical regions of the world. Production of cassava is significantly hampered by cassava brown streak disease (CBSD), caused by Cassava brown streak virus (CBSV) and Ugandan cassava brown streak virus (UCBSV). The di...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5093738/ https://www.ncbi.nlm.nih.gov/pubmed/27808114 http://dx.doi.org/10.1038/srep36164 |
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author | Alicai, Titus Ndunguru, Joseph Sseruwagi, Peter Tairo, Fred Okao-Okuja, Geoffrey Nanvubya, Resty Kiiza, Lilliane Kubatko, Laura Kehoe, Monica A. Boykin, Laura M. |
author_facet | Alicai, Titus Ndunguru, Joseph Sseruwagi, Peter Tairo, Fred Okao-Okuja, Geoffrey Nanvubya, Resty Kiiza, Lilliane Kubatko, Laura Kehoe, Monica A. Boykin, Laura M. |
author_sort | Alicai, Titus |
collection | PubMed |
description | Cassava is a major staple food for about 800 million people in the tropics and sub-tropical regions of the world. Production of cassava is significantly hampered by cassava brown streak disease (CBSD), caused by Cassava brown streak virus (CBSV) and Ugandan cassava brown streak virus (UCBSV). The disease is suppressing cassava yields in eastern Africa at an alarming rate. Previous studies have documented that CBSV is more devastating than UCBSV because it more readily infects both susceptible and tolerant cassava cultivars, resulting in greater yield losses. Using whole genome sequences from NGS data, we produced the first coalescent-based species tree estimate for CBSV and UCBSV. This species framework led to the finding that CBSV has a faster rate of evolution when compared with UCBSV. Furthermore, we have discovered that in CBSV, nonsynonymous substitutions are more predominant than synonymous substitution and occur across the entire genome. All comparative analyses between CBSV and UCBSV presented here suggest that CBSV may be outsmarting the cassava immune system, thus making it more devastating and harder to control. |
format | Online Article Text |
id | pubmed-5093738 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50937382016-11-10 Cassava brown streak virus has a rapidly evolving genome: implications for virus speciation, variability, diagnosis and host resistance Alicai, Titus Ndunguru, Joseph Sseruwagi, Peter Tairo, Fred Okao-Okuja, Geoffrey Nanvubya, Resty Kiiza, Lilliane Kubatko, Laura Kehoe, Monica A. Boykin, Laura M. Sci Rep Article Cassava is a major staple food for about 800 million people in the tropics and sub-tropical regions of the world. Production of cassava is significantly hampered by cassava brown streak disease (CBSD), caused by Cassava brown streak virus (CBSV) and Ugandan cassava brown streak virus (UCBSV). The disease is suppressing cassava yields in eastern Africa at an alarming rate. Previous studies have documented that CBSV is more devastating than UCBSV because it more readily infects both susceptible and tolerant cassava cultivars, resulting in greater yield losses. Using whole genome sequences from NGS data, we produced the first coalescent-based species tree estimate for CBSV and UCBSV. This species framework led to the finding that CBSV has a faster rate of evolution when compared with UCBSV. Furthermore, we have discovered that in CBSV, nonsynonymous substitutions are more predominant than synonymous substitution and occur across the entire genome. All comparative analyses between CBSV and UCBSV presented here suggest that CBSV may be outsmarting the cassava immune system, thus making it more devastating and harder to control. Nature Publishing Group 2016-11-03 /pmc/articles/PMC5093738/ /pubmed/27808114 http://dx.doi.org/10.1038/srep36164 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Alicai, Titus Ndunguru, Joseph Sseruwagi, Peter Tairo, Fred Okao-Okuja, Geoffrey Nanvubya, Resty Kiiza, Lilliane Kubatko, Laura Kehoe, Monica A. Boykin, Laura M. Cassava brown streak virus has a rapidly evolving genome: implications for virus speciation, variability, diagnosis and host resistance |
title | Cassava brown streak virus has a rapidly evolving genome: implications for virus speciation, variability, diagnosis and host resistance |
title_full | Cassava brown streak virus has a rapidly evolving genome: implications for virus speciation, variability, diagnosis and host resistance |
title_fullStr | Cassava brown streak virus has a rapidly evolving genome: implications for virus speciation, variability, diagnosis and host resistance |
title_full_unstemmed | Cassava brown streak virus has a rapidly evolving genome: implications for virus speciation, variability, diagnosis and host resistance |
title_short | Cassava brown streak virus has a rapidly evolving genome: implications for virus speciation, variability, diagnosis and host resistance |
title_sort | cassava brown streak virus has a rapidly evolving genome: implications for virus speciation, variability, diagnosis and host resistance |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5093738/ https://www.ncbi.nlm.nih.gov/pubmed/27808114 http://dx.doi.org/10.1038/srep36164 |
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