# Genotype-specific responses of maize plants to Funneliformis mosseae under drought stress: phenomic and transcriptomic insights

## TL;DR

This study explores how different maize genotypes respond to a specific fungus under drought stress, revealing distinct strategies for improving drought resilience.

## Contribution

The study identifies genotype-specific molecular mechanisms through which arbuscular mycorrhizal fungi enhance drought tolerance in maize.

## Key findings

- Drought-tolerant maize genotype K1 maintains photosynthetic stability with fungal support, while sensitive genotype K2 benefits from root plasticity.
- Hybrid KH shows biomass stability through selective gene activation, with limited fungal impact on hybrid vigor.
- AMF responses are genotype-dependent, suggesting tailored AMF–genotype combinations can improve drought resilience in maize.

## Abstract

Drought is a major abiotic constraint limiting maize productivity, yet the genotype-specific mechanisms through which arbuscular mycorrhizal fungi (AMF) enhance drought resilience remain poorly understood. This study aimed to elucidate how AMF modulate drought tolerance, root plasticity, and heterosis in maize genotypes with contrasting drought sensitivity.

Two maize inbred lines differing in drought tolerance (K1, tolerant; K2, sensitive) and their hybrid (KH) were grown under controlled pot conditions at either well-watered (60% soil moisture) or drought-stressed (30% soil moisture) levels, with or without inoculation with Funneliformis mosseae (BEG12). Integrated phenomic, biomass, and transcriptomic analyses were performed to characterize genotype-specific AMF responses.

AMF induced distinct, genotype-dependent responses under drought stress. In K1 plants, AMF maintained drought tolerance by stabilizing photosynthetic performance, supported by sustained expression of PSI, PSII, LHCb, and Calvin-cycle genes, alongside the activation of CYP450 71A1 and CONSTANS-like 3, suggesting auxin-associated regulation of stress adaptation. In contrast, drought strongly suppressed photosynthetic gene expression in K2 plants, while AMF promoted pronounced root system expansion accompanied by the induction of indole-3-acetaldehyde oxidase, auxin-binding protein 1, CORONATINE-INSENSITIVE 1, and tasselseed-2, indicating hormone-driven root plasticity and modified reproductive signaling. In the hybrid KH, selective activation of RbcX and heterosis-associated genes supported biomass stability and consistent flowering, although AMF had limited effects on hybrid vigor.

These findings reveal distinct molecular strategies underlying AMF-mediated drought resilience in maize, demonstrating that drought-sensitive genotypes primarily benefit through enhanced root plasticity, whereas drought-tolerant genotypes maintain photosynthetic stability. Overall, the results highlight the potential of targeted AMF–genotype combinations to improve water-use efficiency and promote sustainable maize production under drought stress.