# Genome-wide association studies unravel genomic regions and candidate genes associated with Aspergillus flavus resistance in peanut kernels

**Authors:** Mengjie Cui, Jingkun Guo, Feiyan Qi, Ziqi Sun, Linjie Chen, Zheng Wu, Xiangru Xu, Xiaobo Wang, Meng Zhang, Bingyan Huang, Wenzhao Dong, Xinyou Zhang, Suoyi Han

PMC · DOI: 10.1007/s00122-026-05207-8 · TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik · 2026-03-24

## TL;DR

This study identifies genetic markers and candidate genes in peanuts that help resist Aspergillus flavus infection and aflatoxin production, aiding in breeding safer peanut varieties.

## Contribution

The study discovers 10 SNPs, 3 QTLs, and 3 candidate genes linked to peanut resistance to A. flavus and aflatoxin production.

## Key findings

- Three stable QTLs were identified on chromosomes A03 and A05 associated with resistance to A. flavus and aflatoxin production.
- Three candidate genes with favorable haplotypes were validated for their role in resistance and are suitable for marker-assisted breeding.
- Thirteen resistant peanut accessions were identified across three environments, providing valuable germplasm resources.

## Abstract

In the present study, we identified 10 significant single nucleotide polymorphisms (SNPs), 3 stable quantitative trait loci (QTLs) and 3 potential candidate genes associated with peanut kernel resistance to Aspergillus flavus stress.

Peanut (Arachis hypogaea L.) is highly susceptible to A. flavus infection, producing highly carcinogenic aflatoxins. Breeding resistant varieties is an effective and sustainable approach to address this issue, and identifying novel genetic sources and loci underlying resistance is crucial. In this study, 353 A. hypogaea accessions were evaluated for resistance to A. flavus infection and aflatoxin production across three environments, leading to the identification of 13 accessions with stable resistance to both infection and aflatoxin production. A genome-wide association study (GWAS) was performed by integrating phenotypic data from multiple environments with 935,231 SNP markers, resulting in the detection of 10 significant marker-trait associations (MTAs). Of these, one showed consistent association with infection resistance in at least two out of three environments, and two were associated with resistance to both aflatoxin B1 (AFB1) and aflatoxin B2 (AFB2) production. Based on linkage disequilibrium (LD) decay estimates (70 kb upstream and downstream of significant SNPs), three novel stable QTLs were identified on chromosomes A03 and A05, designated qII_A05, qAF_A03, and qAF_A05, and 13 candidate genes were initially selected within these QTL regions. Haplotype analysis further validated 3 key candidate genes: Arahy.7046BI.1 (encoding a PH/START domain-containing protein), Arahy.TX2FLU.1 (encoding a receptor-like kinase), and Arahy.ASR4JM.1 (encoding a TIR-NBS-LRR class disease resistance protein). These genes exhibited significant haplotype-trait associations, with favorable haplotypes showing high frequencies (85.43%–94.12%) in the germplasm pool, facilitating their direct utilization in breeding. Overall, this study uncovers key genetic loci and candidate genes governing peanut resistance to A. flavus infection and aflatoxin production, provides elite resistant germplasm resources, and offers practical insights for marker-assisted selection. The findings lay a solid foundation for accelerating the development of A. flavus-resistant peanut varieties and provide valuable genetic information for peanut breeding programs.

The online version contains supplementary material available at 10.1007/s00122-026-05207-8.

## Linked entities

- **Proteins:** RLK (receptor-like kinase)
- **Chemicals:** aflatoxin B1 (PubChem CID 186907), aflatoxin B2 (PubChem CID 2724360)
- **Species:** Arachis hypogaea (taxon 3818), Aspergillus flavus (taxon 5059)

## Full-text entities

- **Diseases:** carcinogens (MESH:D011230), toxicity (MESH:D064420), A. flavus infection (MESH:D007239), fungal (MESH:D009181)
- **Chemicals:** Tween-80 (MESH:D011136), aflatoxin B2 (MESH:C029753), N2 (MESH:D009584), ammonium acetate (MESH:C018824), water (MESH:D014867), SA (MESH:D020156), acetonitrile (MESH:C032159), AFB1 (MESH:D016604), oil (MESH:D009821), methanol (MESH:D000432), salt (MESH:D012492), lipid (MESH:D008055), agar (MESH:D000362), Aflatoxin (MESH:D000348), AFB2 (-), ethanol (MESH:D000431)
- **Species:** Cicer arietinum (chickpea, species) [taxon 3827], Arachis hypogaea subsp. hypogaea (subspecies) [taxon 226205], A. flavus [taxon 315677], Homo sapiens (human, species) [taxon 9606], Arachis hypogaea (goober, species) [taxon 3818], Oryza sativa (Asian cultivated rice, species) [taxon 4530], Aspergillus flavus (species) [taxon 5059], Arabidopsis thaliana (mouse-ear cress, species) [taxon 3702]
- **Cell lines:** As3.4408 — Homo sapiens (Human), Bloom syndrome, Transformed cell line (CVCL_7408)

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC13013137