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. 2024 May 2:15:1348168.
doi: 10.3389/fpls.2024.1348168. eCollection 2024.

Discovering new genes for alfalfa (Medicago sativa) growth and biomass resilience in combined salinity and Phoma medicaginis infection through GWAS

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Discovering new genes for alfalfa (Medicago sativa) growth and biomass resilience in combined salinity and Phoma medicaginis infection through GWAS

Wiem Mnafgui et al. Front Plant Sci. .

Abstract

Salinity and Phoma medicaginis infection represent significant challenges for alfalfa cultivation in South Africa, Europe, Australia, and, particularly, Tunisia. These constraints have a severe impact on both yield and quality. The primary aim of this study was to establish the genetic basis of traits associated with biomass and growth of 129 Medicago sativa genotypes through genome-wide association studies (GWAS) under combined salt and P. medicaginis infection stresses. The results of the analysis of variance (ANOVA) indicated that the variation in these traits could be primarily attributed to genotype effects. Among the test genotypes, the length of the main stem, the number of ramifications, the number of chlorotic leaves, and the aerial fresh weight exhibited the most significant variation. The broad-sense heritability (H²) was relatively high for most of the assessed traits, primarily due to genetic factors. Cluster analysis, applied to morpho-physiological traits under the combined stresses, revealed three major groups of accessions. Subsequently, a GWAS analysis was conducted to validate significant associations between 54,866 SNP-filtered single-nucleotide polymorphisms (SNPs) and seven traits. The study identified 27 SNPs that were significantly associated with the following traits: number of healthy leaves (two SNPs), number of chlorotic leaves (five SNPs), number of infected necrotic leaves (three SNPs), aerial fresh weight (six SNPs), aerial dry weight (nine SNPs), number of ramifications (one SNP), and length of the main stem (one SNP). Some of these markers are related to the ionic transporters, cell membrane rigidity (related to salinity tolerance), and the NBS_LRR gene family (associated with disease resistance). These findings underscore the potential for selecting alfalfa genotypes with tolerance to the combined constraints of salinity and P. medicaginis infection.

Keywords: GWAS; Phoma medicaginis; alfalfa; biomass traits; genetic resources; salinity; stress tolerance.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
Two-dimensional PCA plot showing the relationships among measured traits (A) for the accessions (B) and Biplot (genotype, trait) (C) representing alfalfa (Medicago sativa) under a combination of salinity and Phoma medicaginis (Strain Pm8) infection. Length of medium stem (LMS, cm), number of ramifications (NR), number of healthy leaves (NHL), number of chlorotic leaves (NCL), number of chlorotic necrotic leaves (NCNL), aerial fresh weight (AFW, g), and aerial dry weight (ADW, g).
Figure 2
Figure 2
Manhattan plots of marker–trait associations for tolerance traits of alfalfa (M. sativa) to a combination of salinity and Phoma medicaginis (strain Pm8) infection. Significant markers that passed a cutoff log (p-value) of 4. The X-axis represents the physical location of SNPs on chromosomes (color-coded) and the Y-axis represents the −log10 p-value of SNP phenotype associations. (A) length of the main stem (LMS, cm); (B) number of ramifications (NR), (C) aerial fresh weight (AFW, g) and (D) aerial dry weight (ADW, g).
Figure 3
Figure 3
Manhattan plots of marker–trait associations for tolerance traits of alfalfa (M. sativa) to a combination of salinity and Phoma medicaginis (Strain Pm8) infection. Significant markers that passed a cutoff log (p-value) of 4. The X-axis represents the physical location of SNPs on chromosomes (color-coded) and the Y-axis represents the −log10 p-value of SNP phenotype associations. (A) number of chlorotic leaves (NCL); (B) number of chlorotic necrotic leaves (NCNL); (C) number of healthy leaves (NHL).

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Grants and funding

The authors declare financial support was received for the research, authorship, and/or publication of this article. This research was funded by the Tunisian-South African project (2019-2024) and the Tunisian Ministry of Higher Education and Scientific Research (LR15 CBBC02). The plant material was generated by the FP7-ArimNet project REFORMA funded by the Governments of Italy, Algeria, Morocco and Tunisia.
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