Arbuscular mycorrhizal fungi (AMF) establish symbiotic interaction with 80% of known land plants. It has a pronounced impact on plant growth, water absorption, mineral nutrition, and protection from abiotic stresses. Plants are very dynamic systems having great adaptability under continuously changing drying conditions. In this regard, the function of AMF as a biological tool for improving plant drought stress tolerance and phenotypic plasticity, in terms of establishing mutualistic associations, seems an innovative approach towards sustainable agriculture. However, a better understanding of these complex interconnected signaling pathways and AMF-mediated mechanisms that regulate the drought tolerance in plants will enhance its potential application as an innovative approach in environmentally friendly agriculture. This paper reviews the underlying mechanisms that are confidently linked with plant–AMF interaction in alleviating drought stress, constructing emphasis on phytohormones and signaling molecules and their interaction with biochemical, and physiological processes to maintain the homeostasis of nutrient and water cycling and plant growth performance. Likewise, the paper will analyze how the AMF symbiosis helps the plant to overcome the deleterious effects of stress is also evaluated. Finally, we review how interactions between various signaling mechanisms governed by AMF symbiosis modulate different physiological responses to improve drought tolerance. Understanding the AMF-mediated mechanisms that are important for regulating the establishment of the mycorrhizal association and the plant protective responses towards unfavorable conditions will open new approaches to exploit AMF as a bioprotective tool against drought.

Arbuscular mycorrhizal fungi (AMF) and rhizobia play a pivotal role in enhancing crop productivity, shaping microbial community structure, and improving soil quality, making them key components for sustainable ecosystem development. The symbiotic relationship between AMF and rhizobia is crucial for facilitating efficient biological nitrogen fixation and nutrient absorption, thereby reducing the dependence on chemical fertilizers and promoting sustainable agricultural practices. The findings of various studies, however, indicate that soil environment can impede the symbiotic relationship between AMF and rhizobia. We conducted a comprehensive meta-analysis of 158 articles from 1980 to 2022 to explore the synergistic interactions in legume–AMF–rhizobium systems and the potential mechanisms underlying this synergism. Our findings revealed that the inoculation with AMF and/or rhizobia significantly (p < 0.001) increased legume plant nitrogen content, phosphorus content, shoot biomass, yield, AMF colonization rate, and the number and weight of nodules compared to uninoculated controls (effect size d > 0). Moreover, there was a substantial synergistic effect between AMF and rhizobia (p < 0.001). Nevertheless, soil salinity stress, drought stress, and pH stress could hinder the positive effects of inoculation treatments, possibly due to the plant trade-off strategies under abiotic stress conditions. This research may potentially lead to new solutions for sustainable agricultural systems amidst the challenges posed by global climate change.

Around 85% of all land plants have symbiotic relationships with arbuscular mycorrhizal (AM) fungi, microscopic soil fungi that build extensive filamentous network in and around the roots. These links strongly influence plant development, water uptake, mineral nutrition, and defense against abiotic stresses. In this context, the use of AMF as a biological instrument to enhance plant drought resistance and phenotypic plasticity, through the formation of mutualistic associations, seems like a novel strategy for sustainable agriculture. This review synthesizes current understanding on the mechanisms through which AMF alleviates drought stress in agriculture. We focus on how AMF help maintain nutrient and water homeostasis by modulating phytohormones and signaling molecules, and by orchestrating associated biochemical and physiological responses. Particular emphasis is placed on aquaporins (AQPs) as key water-and stress-related channels whose expression and activity are modulated by AMF to maintain ion, nutrient, and water balance. AMF-mediated host AQP responses exhibit three unique patterns under stressful conditions: either no changes, downregulation to limit water loss, or upregulation to promote water and nutrient uptake. Nevertheless, little is known about cellular and molecular underpinnings of AMF effect on host AQPs. We also summarize evidence that AMF enhance antioxidant defenses, osmotic adjustment, soil structure, and water retention, thereby jointly improving plant drought tolerance. This review concludes by outlining the potential of AMF to support sustainable agriculture, offering critical research gaps, such as mechanistic studies on fungal AQPs, hormonal crosstalk, and field-scale performance, which propose future directions for deploying AMF in drought-prone agroecosystems.

Arbuscular mycorrhizal fungi (AMF) and rhizobia are crucial for plant productivity, microbial community structure, and soil quality, making them key components for sustainable ecosystem development. The symbiotic relationship between AMF and rhizobia is essential for effective biological nitrogen fixation and nutrient absorption, reducing reliance on chemical fertilizers and promoting sustainable agricultural practices. However, studies have shown that soil environment can hinder the symbiotic relationship between AMF and rhizobia. We conducted a meta-analysis of 158 articles from 1980 to 2022 to explore the synergistic interactions in legume-AMF-rhizobium systems and the potential mechanisms underlying synergism. Our findings revealed that the inoculation with AMF and/or rhizobia significantly (P < 0.001) increased legume plant nitrogen content, phosphorus content, shoot biomass, yield, AMF colonization rate, nodule number, and nodule weight compared to uninoculated controls (effect size d >0). There was a substantial synergistic effect between AMF and rhizobia (P < 0.001). However, soil salt, drought and pH stress inhibited the positive effects of inoculation treatments, possibly due to the plant trade off strategies under adverse stress conditions. Under well-watered condition, the d values of plant yield in the rhizobia, AMF and co-inoculation treatments were 2.047, 1.661, and 3.412 (QM = 246, P < 0.001), respectively, which were higher than that of 1.196, 0.765, and 1.828 (QM = 195, P < 0.001) in the drought stress treatment. This research may potentially lead to new solutions for sustainable agricultural systems in the face of global climate change.

Purple acid phosphatases (PAPs) play a key role in phosphorus (P) assimilation and redistribution in plants, catalyzing the hydrolysis of phosphate esters to produce inorganic phosphate (Pi). In this study, a total of 77 PAP genes were identified in B. napus. The candidate genes were divided into three groups and ten subgroups based on the phylogenetic analyses and exon-intron organization. Among these 77 BnaPAP proteins, 35 exhibit typical metal-ligating residues characteristic of known PAPs, whereas certain unaltered amino acid residues were absent or displaced in other BnaPAPs. A computational prediction was conducted, revealing that the majority of PAPs contain signal peptide motifs and display a range of N-glycosylation levels, as well as transmembrane helix motifs. An analysis of previously obtained RNA-seq data revealed that 55.84% (43 of 77) of the BnaPAPs responded to Pi deficiency. Moreover, we conducted a preliminary examination of the expression profiles of BnaPAP genes in response to salt stress, and discovered that 42.86% (33 of 77) of these genes were induced under salt stress, either in the shoots or in the roots. Further qRT-PCR and GUS analyses revealed that BnaC9.PAP10 and BnaA7.PAP10, two paralogs of BnaPAP10s, were induced by Pi deficiency. Notably, BnaC9.PAP10 exhibits robust induction, compared to the relatively mild induction observed in BnaA7.PAP10. Our research shows that BnaA7.PAP10 uniquely responds to Pi stress via the W-box, while BnaA7.PAP10 predominantly responds via the P1BS element, and the differences in cis-regulatory elements (CREs) within their promoter regions specifically contribute to their distinct expression levels under Pi stress. Our findings provide valuable insights and establish a foundation for future functional studies of BnaPAPs.