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Genome-wide association of rice response to blast fungus identifies loci for robust resistance under high nitrogen

BACKGROUND: Nitrogen fertilization is known to increase disease susceptibility, a phenomenon called Nitrogen-Induced Susceptibility (NIS). In rice, this phenomenon has been observed in infections with the blast fungus Magnaporthe oryzae. A previous classical genetic study revealed a locus (NIS1) tha...

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Autores principales: Frontini, Mathias, Boisnard, Arnaud, Frouin, Julien, Ouikene, Malika, Morel, Jean Benoit, Ballini, Elsa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7893971/
https://www.ncbi.nlm.nih.gov/pubmed/33602120
http://dx.doi.org/10.1186/s12870-021-02864-3
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author Frontini, Mathias
Boisnard, Arnaud
Frouin, Julien
Ouikene, Malika
Morel, Jean Benoit
Ballini, Elsa
author_facet Frontini, Mathias
Boisnard, Arnaud
Frouin, Julien
Ouikene, Malika
Morel, Jean Benoit
Ballini, Elsa
author_sort Frontini, Mathias
collection PubMed
description BACKGROUND: Nitrogen fertilization is known to increase disease susceptibility, a phenomenon called Nitrogen-Induced Susceptibility (NIS). In rice, this phenomenon has been observed in infections with the blast fungus Magnaporthe oryzae. A previous classical genetic study revealed a locus (NIS1) that enhances susceptibility to rice blast under high nitrogen fertilization. In order to further address the underlying genetics of plasticity in susceptibility to rice blast after fertilization, we analyzed NIS under greenhouse-controlled conditions in a panel of 139 temperate japonica rice strains. A genome-wide association analysis was conducted to identify loci potentially involved in NIS by comparing susceptibility loci identified under high and low nitrogen conditions, an approach allowing for the identification of loci validated across different nitrogen environments. We also used a novel NIS Index to identify loci potentially contributing to plasticity in susceptibility under different nitrogen fertilization regimes. RESULTS: A global NIS effect was observed in the population, with the density of lesions increasing by 8%, on average, under high nitrogen fertilization. Three new QTL, other than NIS1, were identified. A rare allele of the RRobN1 locus on chromosome 6 provides robust resistance in high and low nitrogen environments. A frequent allele of the NIS2 locus, on chromosome 5, exacerbates blast susceptibility under the high nitrogen condition. Finally, an allele of NIS3, on chromosome 10, buffers the increase of susceptibility arising from nitrogen fertilization but increases global levels of susceptibility. This allele is almost fixed in temperate japonicas, as a probable consequence of genetic hitchhiking with a locus involved in cold stress adaptation. CONCLUSIONS: Our results extend to an entire rice subspecies the initial finding that nitrogen increases rice blast susceptibility. We demonstrate the usefulness of estimating plasticity for the identification of novel loci involved in the response of rice to the blast fungus under different nitrogen regimes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12870-021-02864-3.
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spelling pubmed-78939712021-02-22 Genome-wide association of rice response to blast fungus identifies loci for robust resistance under high nitrogen Frontini, Mathias Boisnard, Arnaud Frouin, Julien Ouikene, Malika Morel, Jean Benoit Ballini, Elsa BMC Plant Biol Research Article BACKGROUND: Nitrogen fertilization is known to increase disease susceptibility, a phenomenon called Nitrogen-Induced Susceptibility (NIS). In rice, this phenomenon has been observed in infections with the blast fungus Magnaporthe oryzae. A previous classical genetic study revealed a locus (NIS1) that enhances susceptibility to rice blast under high nitrogen fertilization. In order to further address the underlying genetics of plasticity in susceptibility to rice blast after fertilization, we analyzed NIS under greenhouse-controlled conditions in a panel of 139 temperate japonica rice strains. A genome-wide association analysis was conducted to identify loci potentially involved in NIS by comparing susceptibility loci identified under high and low nitrogen conditions, an approach allowing for the identification of loci validated across different nitrogen environments. We also used a novel NIS Index to identify loci potentially contributing to plasticity in susceptibility under different nitrogen fertilization regimes. RESULTS: A global NIS effect was observed in the population, with the density of lesions increasing by 8%, on average, under high nitrogen fertilization. Three new QTL, other than NIS1, were identified. A rare allele of the RRobN1 locus on chromosome 6 provides robust resistance in high and low nitrogen environments. A frequent allele of the NIS2 locus, on chromosome 5, exacerbates blast susceptibility under the high nitrogen condition. Finally, an allele of NIS3, on chromosome 10, buffers the increase of susceptibility arising from nitrogen fertilization but increases global levels of susceptibility. This allele is almost fixed in temperate japonicas, as a probable consequence of genetic hitchhiking with a locus involved in cold stress adaptation. CONCLUSIONS: Our results extend to an entire rice subspecies the initial finding that nitrogen increases rice blast susceptibility. We demonstrate the usefulness of estimating plasticity for the identification of novel loci involved in the response of rice to the blast fungus under different nitrogen regimes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12870-021-02864-3. BioMed Central 2021-02-18 /pmc/articles/PMC7893971/ /pubmed/33602120 http://dx.doi.org/10.1186/s12870-021-02864-3 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Frontini, Mathias
Boisnard, Arnaud
Frouin, Julien
Ouikene, Malika
Morel, Jean Benoit
Ballini, Elsa
Genome-wide association of rice response to blast fungus identifies loci for robust resistance under high nitrogen
title Genome-wide association of rice response to blast fungus identifies loci for robust resistance under high nitrogen
title_full Genome-wide association of rice response to blast fungus identifies loci for robust resistance under high nitrogen
title_fullStr Genome-wide association of rice response to blast fungus identifies loci for robust resistance under high nitrogen
title_full_unstemmed Genome-wide association of rice response to blast fungus identifies loci for robust resistance under high nitrogen
title_short Genome-wide association of rice response to blast fungus identifies loci for robust resistance under high nitrogen
title_sort genome-wide association of rice response to blast fungus identifies loci for robust resistance under high nitrogen
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7893971/
https://www.ncbi.nlm.nih.gov/pubmed/33602120
http://dx.doi.org/10.1186/s12870-021-02864-3
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