Evidence map›Paper›PMID 33602120›Full record

ArticleBMC plant biology2021

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

Mathias Frontini, Arnaud Boisnard, Julien Frouin, Malika Ouikene, Jean Benoit Morel, Elsa Ballini

Open access · goldAbstract read
In one paragraph

Article in BMC plant biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
4.2field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 21 citations in OpenAlex.

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  5. Identification of significant SNPs and candidate loci for blast disease resistance via GWAS and population structure analysis in ARC panel ofPhysiology and molecular biology of plants : an international journal of functional plant biology · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Mathias FrontiniBGPI, Univ Montpellier, CIRAD, INRAE, Institut Agro, Montpellier, France.
Arnaud BoisnardCentre Français du Riz, Arles, France.
Julien FrouinAGAP, Univ Montpellier, CIRAD, INRAE, Institut Agro, Montpellier, France.
Malika OuikeneGroupe de Valorisation des Produits Agricoles (GVAPRO), Alger, Algeria.
Jean Benoit MorelBGPI, Univ Montpellier, CIRAD, INRAE, Institut Agro, Montpellier, France.ORCID https://orcid.org/0000-0003-1988-956X
Elsa BalliniBGPI, Univ Montpellier, CIRAD, INRAE, Institut Agro, Montpellier, France. elsa.ballini@supagro.fr.ORCID http://orcid.org/0000-0002-2571-2069
Centre de Coopération Internationale en Recherche Agronomique pour le Développement · FRCentre d’Étude et de Valorisation des Algues · FRCentre Français des Fonds et Fondations · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNitrogen 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.

resultsA 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.

conclusionsOur 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.

Indexed as

AllelesAscomycotaDisease ResistanceGenome, PlantGenome-Wide Association StudyNitrogenOryzaPlant DiseasesPlant ProteinsQuantitative Trait LociNitrogenPlant ProteinsGWASMagnaporthe oryzaeNitrogenRiceRobustness, temperate japonica rice, rice blast, induced susceptibility

Identifiers

PMID33602120
PMCPMC7893971
OpenAlexW3131765819

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.