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Genome Analyses of an Aggressive and Invasive Lineage of the Irish Potato Famine Pathogen

Pest and pathogen losses jeopardise global food security and ever since the 19(th) century Irish famine, potato late blight has exemplified this threat. The causal oomycete pathogen, Phytophthora infestans, undergoes major population shifts in agricultural systems via the successive emergence and mi...

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Autores principales: Cooke, David E. L., Cano, Liliana M., Raffaele, Sylvain, Bain, Ruairidh A., Cooke, Louise R., Etherington, Graham J., Deahl, Kenneth L., Farrer, Rhys A., Gilroy, Eleanor M., Goss, Erica M., Grünwald, Niklaus J., Hein, Ingo, MacLean, Daniel, McNicol, James W., Randall, Eva, Oliva, Ricardo F., Pel, Mathieu A., Shaw, David S., Squires, Julie N., Taylor, Moray C., Vleeshouwers, Vivianne G. A. A., Birch, Paul R. J., Lees, Alison K., Kamoun, Sophien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3464212/
https://www.ncbi.nlm.nih.gov/pubmed/23055926
http://dx.doi.org/10.1371/journal.ppat.1002940
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author Cooke, David E. L.
Cano, Liliana M.
Raffaele, Sylvain
Bain, Ruairidh A.
Cooke, Louise R.
Etherington, Graham J.
Deahl, Kenneth L.
Farrer, Rhys A.
Gilroy, Eleanor M.
Goss, Erica M.
Grünwald, Niklaus J.
Hein, Ingo
MacLean, Daniel
McNicol, James W.
Randall, Eva
Oliva, Ricardo F.
Pel, Mathieu A.
Shaw, David S.
Squires, Julie N.
Taylor, Moray C.
Vleeshouwers, Vivianne G. A. A.
Birch, Paul R. J.
Lees, Alison K.
Kamoun, Sophien
author_facet Cooke, David E. L.
Cano, Liliana M.
Raffaele, Sylvain
Bain, Ruairidh A.
Cooke, Louise R.
Etherington, Graham J.
Deahl, Kenneth L.
Farrer, Rhys A.
Gilroy, Eleanor M.
Goss, Erica M.
Grünwald, Niklaus J.
Hein, Ingo
MacLean, Daniel
McNicol, James W.
Randall, Eva
Oliva, Ricardo F.
Pel, Mathieu A.
Shaw, David S.
Squires, Julie N.
Taylor, Moray C.
Vleeshouwers, Vivianne G. A. A.
Birch, Paul R. J.
Lees, Alison K.
Kamoun, Sophien
author_sort Cooke, David E. L.
collection PubMed
description Pest and pathogen losses jeopardise global food security and ever since the 19(th) century Irish famine, potato late blight has exemplified this threat. The causal oomycete pathogen, Phytophthora infestans, undergoes major population shifts in agricultural systems via the successive emergence and migration of asexual lineages. The phenotypic and genotypic bases of these selective sweeps are largely unknown but management strategies need to adapt to reflect the changing pathogen population. Here, we used molecular markers to document the emergence of a lineage, termed 13_A2, in the European P. infestans population, and its rapid displacement of other lineages to exceed 75% of the pathogen population across Great Britain in less than three years. We show that isolates of the 13_A2 lineage are among the most aggressive on cultivated potatoes, outcompete other aggressive lineages in the field, and overcome previously effective forms of plant host resistance. Genome analyses of a 13_A2 isolate revealed extensive genetic and expression polymorphisms particularly in effector genes. Copy number variations, gene gains and losses, amino-acid replacements and changes in expression patterns of disease effector genes within the 13_A2 isolate likely contribute to enhanced virulence and aggressiveness to drive this population displacement. Importantly, 13_A2 isolates carry intact and in planta induced Avrblb1, Avrblb2 and Avrvnt1 effector genes that trigger resistance in potato lines carrying the corresponding R immune receptor genes Rpi-blb1, Rpi-blb2, and Rpi-vnt1.1. These findings point towards a strategy for deploying genetic resistance to mitigate the impact of the 13_A2 lineage and illustrate how pathogen population monitoring, combined with genome analysis, informs the management of devastating disease epidemics.
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spelling pubmed-34642122012-10-09 Genome Analyses of an Aggressive and Invasive Lineage of the Irish Potato Famine Pathogen Cooke, David E. L. Cano, Liliana M. Raffaele, Sylvain Bain, Ruairidh A. Cooke, Louise R. Etherington, Graham J. Deahl, Kenneth L. Farrer, Rhys A. Gilroy, Eleanor M. Goss, Erica M. Grünwald, Niklaus J. Hein, Ingo MacLean, Daniel McNicol, James W. Randall, Eva Oliva, Ricardo F. Pel, Mathieu A. Shaw, David S. Squires, Julie N. Taylor, Moray C. Vleeshouwers, Vivianne G. A. A. Birch, Paul R. J. Lees, Alison K. Kamoun, Sophien PLoS Pathog Research Article Pest and pathogen losses jeopardise global food security and ever since the 19(th) century Irish famine, potato late blight has exemplified this threat. The causal oomycete pathogen, Phytophthora infestans, undergoes major population shifts in agricultural systems via the successive emergence and migration of asexual lineages. The phenotypic and genotypic bases of these selective sweeps are largely unknown but management strategies need to adapt to reflect the changing pathogen population. Here, we used molecular markers to document the emergence of a lineage, termed 13_A2, in the European P. infestans population, and its rapid displacement of other lineages to exceed 75% of the pathogen population across Great Britain in less than three years. We show that isolates of the 13_A2 lineage are among the most aggressive on cultivated potatoes, outcompete other aggressive lineages in the field, and overcome previously effective forms of plant host resistance. Genome analyses of a 13_A2 isolate revealed extensive genetic and expression polymorphisms particularly in effector genes. Copy number variations, gene gains and losses, amino-acid replacements and changes in expression patterns of disease effector genes within the 13_A2 isolate likely contribute to enhanced virulence and aggressiveness to drive this population displacement. Importantly, 13_A2 isolates carry intact and in planta induced Avrblb1, Avrblb2 and Avrvnt1 effector genes that trigger resistance in potato lines carrying the corresponding R immune receptor genes Rpi-blb1, Rpi-blb2, and Rpi-vnt1.1. These findings point towards a strategy for deploying genetic resistance to mitigate the impact of the 13_A2 lineage and illustrate how pathogen population monitoring, combined with genome analysis, informs the management of devastating disease epidemics. Public Library of Science 2012-10-04 /pmc/articles/PMC3464212/ /pubmed/23055926 http://dx.doi.org/10.1371/journal.ppat.1002940 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Cooke, David E. L.
Cano, Liliana M.
Raffaele, Sylvain
Bain, Ruairidh A.
Cooke, Louise R.
Etherington, Graham J.
Deahl, Kenneth L.
Farrer, Rhys A.
Gilroy, Eleanor M.
Goss, Erica M.
Grünwald, Niklaus J.
Hein, Ingo
MacLean, Daniel
McNicol, James W.
Randall, Eva
Oliva, Ricardo F.
Pel, Mathieu A.
Shaw, David S.
Squires, Julie N.
Taylor, Moray C.
Vleeshouwers, Vivianne G. A. A.
Birch, Paul R. J.
Lees, Alison K.
Kamoun, Sophien
Genome Analyses of an Aggressive and Invasive Lineage of the Irish Potato Famine Pathogen
title Genome Analyses of an Aggressive and Invasive Lineage of the Irish Potato Famine Pathogen
title_full Genome Analyses of an Aggressive and Invasive Lineage of the Irish Potato Famine Pathogen
title_fullStr Genome Analyses of an Aggressive and Invasive Lineage of the Irish Potato Famine Pathogen
title_full_unstemmed Genome Analyses of an Aggressive and Invasive Lineage of the Irish Potato Famine Pathogen
title_short Genome Analyses of an Aggressive and Invasive Lineage of the Irish Potato Famine Pathogen
title_sort genome analyses of an aggressive and invasive lineage of the irish potato famine pathogen
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3464212/
https://www.ncbi.nlm.nih.gov/pubmed/23055926
http://dx.doi.org/10.1371/journal.ppat.1002940
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