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Random Plant Viral Variants Attain Temporal Advantages During Systemic Infections and in Turn Resist other Variants of the Same Virus

Infection of plants with viruses containing multiple variants frequently leads to dominance by a few random variants in the systemically infected leaves (SLs), for which a plausible explanation is lacking. We show here that SL dominance by a given viral variant is adequately explained by its fortuit...

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Autores principales: Zhang, Xiao-Feng, Guo, Jiangbo, Zhang, Xiuchun, Meulia, Tea, Paul, Pierce, Madden, Laurence V., Li, Dawei, Qu, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4612314/
https://www.ncbi.nlm.nih.gov/pubmed/26481091
http://dx.doi.org/10.1038/srep15346
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author Zhang, Xiao-Feng
Guo, Jiangbo
Zhang, Xiuchun
Meulia, Tea
Paul, Pierce
Madden, Laurence V.
Li, Dawei
Qu, Feng
author_facet Zhang, Xiao-Feng
Guo, Jiangbo
Zhang, Xiuchun
Meulia, Tea
Paul, Pierce
Madden, Laurence V.
Li, Dawei
Qu, Feng
author_sort Zhang, Xiao-Feng
collection PubMed
description Infection of plants with viruses containing multiple variants frequently leads to dominance by a few random variants in the systemically infected leaves (SLs), for which a plausible explanation is lacking. We show here that SL dominance by a given viral variant is adequately explained by its fortuitous lead in systemic spread, coupled with its resistance to superinfection by other variants. We analyzed the fate of a multi-variant turnip crinkle virus (TCV) population in Arabidopsis and N. benthamiana plants. Both wild-type and RNA silencing-defective plants displayed a similar pattern of random dominance by a few variant genotypes, thus discounting a prominent role for RNA silencing. When introduced to plants sequentially as two subpopulations, a twelve-hour head-start was sufficient for the first set to dominate. Finally, SLs of TCV-infected plants became highly resistant to secondary invasions of another TCV variant. We propose that random distribution of variant foci on inoculated leaves allows different variants to lead systemic movement in different plants. The leading variants then colonize large areas of SLs, and resist the superinfection of lagging variants in the same areas. In conclusion, superinfection resistance is the primary driver of random enrichment of viral variants in systemically infected plants.
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spelling pubmed-46123142015-11-02 Random Plant Viral Variants Attain Temporal Advantages During Systemic Infections and in Turn Resist other Variants of the Same Virus Zhang, Xiao-Feng Guo, Jiangbo Zhang, Xiuchun Meulia, Tea Paul, Pierce Madden, Laurence V. Li, Dawei Qu, Feng Sci Rep Article Infection of plants with viruses containing multiple variants frequently leads to dominance by a few random variants in the systemically infected leaves (SLs), for which a plausible explanation is lacking. We show here that SL dominance by a given viral variant is adequately explained by its fortuitous lead in systemic spread, coupled with its resistance to superinfection by other variants. We analyzed the fate of a multi-variant turnip crinkle virus (TCV) population in Arabidopsis and N. benthamiana plants. Both wild-type and RNA silencing-defective plants displayed a similar pattern of random dominance by a few variant genotypes, thus discounting a prominent role for RNA silencing. When introduced to plants sequentially as two subpopulations, a twelve-hour head-start was sufficient for the first set to dominate. Finally, SLs of TCV-infected plants became highly resistant to secondary invasions of another TCV variant. We propose that random distribution of variant foci on inoculated leaves allows different variants to lead systemic movement in different plants. The leading variants then colonize large areas of SLs, and resist the superinfection of lagging variants in the same areas. In conclusion, superinfection resistance is the primary driver of random enrichment of viral variants in systemically infected plants. Nature Publishing Group 2015-10-20 /pmc/articles/PMC4612314/ /pubmed/26481091 http://dx.doi.org/10.1038/srep15346 Text en Copyright © 2015, Macmillan Publishers Limited 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
Zhang, Xiao-Feng
Guo, Jiangbo
Zhang, Xiuchun
Meulia, Tea
Paul, Pierce
Madden, Laurence V.
Li, Dawei
Qu, Feng
Random Plant Viral Variants Attain Temporal Advantages During Systemic Infections and in Turn Resist other Variants of the Same Virus
title Random Plant Viral Variants Attain Temporal Advantages During Systemic Infections and in Turn Resist other Variants of the Same Virus
title_full Random Plant Viral Variants Attain Temporal Advantages During Systemic Infections and in Turn Resist other Variants of the Same Virus
title_fullStr Random Plant Viral Variants Attain Temporal Advantages During Systemic Infections and in Turn Resist other Variants of the Same Virus
title_full_unstemmed Random Plant Viral Variants Attain Temporal Advantages During Systemic Infections and in Turn Resist other Variants of the Same Virus
title_short Random Plant Viral Variants Attain Temporal Advantages During Systemic Infections and in Turn Resist other Variants of the Same Virus
title_sort random plant viral variants attain temporal advantages during systemic infections and in turn resist other variants of the same virus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4612314/
https://www.ncbi.nlm.nih.gov/pubmed/26481091
http://dx.doi.org/10.1038/srep15346
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