Arbuscular mycorrhizal fungi (AMF) are the basis symbionts in terrestrial ecosystems, profoundly influencing plant development, nutrient acquisition, and resilience to biotic and abiotic stresses. This review synthesizes current systematic understandings of AMF-mediated augmentation of plant growth and disease resistance, with a particular emphasis on their role in sustainable crop production. AMF improves host plant performance through enhanced phosphorus, nitrogen, and water uptake via extensive extraradical hyphal networks. Moreover, AMF colonization modulates phytohormonal signaling pathways, including salicylic acid, jasmonic acid, abscisic acid, and nitric oxide, priming SR and upregulating defense-related gene expression. Increased biosynthesis of secondary metabolites, reinforcement of cell walls, and activation of antioxidant enzyme systems often accompany these responses. AMF also engage in synergistic interactions with rhizosphere microbiota such as Trichoderma, Pseudomonas, and Bacillus, enhancing their collective biocontrol efficacy against a broad spectrum of soil-borne pathogens, including fungi, bacteria, and nematodes. Through modulation of root exudates, glomalin-mediated soil aggregation, and microbiome restructuring, AMF contributes to the establishment of disease-suppressive soils. Genomic and transcriptomic studies have elucidated key components of the common symbiosis-signaling pathway, supporting AMF-host specificity and functional outcomes. AMF is a promising biotechnological tool for integrated pest, disease, and nutrient management. Advancing their application in field settings requires targeted research on strain-host-environment interactions, formulation technologies, and long-term ecosystem impacts, aligning AMF-based strategies with the goals of resilient and sustainable agriculture.

Brassica napus (B. napus) is susceptible to multiple abiotic stresses that can affect plant growth and development, ultimately reducing crop yields. In the past, many genes that provide tolerance to abiotic stresses have been identified and characterized. Peroxidase (POD) proteins, members of the oxidoreductase enzyme family, play a critical role in protecting plants against abiotic stresses. This study demonstrated a comprehensive investigation of the POD gene family in B. napus. As a result, a total of 109 POD genes were identified across the 19 chromosomes and classified into five distinct subgroups. Further, 44 duplicate events were identified; of these, two gene pairs were tandem and 42 were segmental. Synteny analysis revealed that segmental duplication was more prominent than tandem duplication among POD genes. Expression pattern analysis based on the RNA-seq data of B. napus indicated that BnPOD genes were expressed differently in various tissues; most of them were expressed in roots rather than in other tissues. To validate these findings, we performed RT-qPCR analysis on ten genes; these genes showed various expression levels under abiotic stresses. Our findings not only furnish valuable insights into the evolutionary dynamics of the BnPOD gene family but also serve as a foundation for subsequent investigations into the functional roles of POD genes in B. napus.

Editorial: Salinity and drought stress in plants: understanding physiological, biochemical and molecular responses

The primary objectives of the development of salt-resilient crops are to investigate, comprehend, and devise strategies to explore the mechanisms of salinity stress. Soil salinity is a major factor limiting plant growth as it induces ion toxicity and nutrient imbalance. Abscisic acid (ABA) is a crucial phytohormone that plays a central role in abiotic stress tolerance, particularly in response to salinity. In this review, we aimed to provide a comprehensive overview of the mechanisms activated by salinity, such as ABA perception and salinity response genes, to modify salinity stress responses. Furthermore, we sought to understand the synergistic role of salt-ABA and other phytohormones in the development of salt-tolerant crops by integrating various biotechnological approaches.

Sugarcane (Saccharum spp. hybrids) is a worldwide acclaimed important agricultural crop used primarily for sugar production and biofuel. Sugarcane’s genetic complexity, aneuploidy, and extreme heterozygosity make it a challenging crop in developing improved varieties. The molecular breeding programs promise to develop nutritionally improved varieties for both direct consumption and commercial application. Therefore, to address these challenges, the development of simple sequence repeats (SSRs) has been proven to be a powerful molecular tool in sugarcane. This study involved the collection of 285216 expressed sequence tags (ESTs) from sugarcane, resulting in 23666 unigenes, including 4547 contigs. Our analysis identified 4120 unigenes containing a total of 4960 SSRs, with the most abundant repeat types being monomeric (44.33%), dimeric (13.10%), and trimeric (39.68%). We further chose 173 primers to analyze the banding pattern in 10 sugarcane accessions by PAGE analysis. Additionally, functional annotation analysis showed that 71.07%, 53.6%, and 10.3% unigenes were annotated by Uniport, GO, and KEGG, respectively. GO annotations and KEGG pathways were distributed across three functional categories: molecular (46.46%), cellular (33.94%), and biological pathways (19.6%). The cluster analysis indicated the formation of four distinct clusters among selected sugarcane accessions, with maximum genetic distance observed among the varieties. We believe that these EST-SSR markers will serve as valuable references for future genetic characterization, species identification, and breeding efforts in sugarcane.

Soil salinity represents a significant abiotic constraint limiting the productivity and geographical expansion of rapeseed (Brassica napus L.), yet the coordination among the signaling, hormonal, metabolic, and regulatory layers underlying salt tolerance remains incompletely understood. This study elucidates the physiological, biochemical, and transcriptomic responses of B. napus inbred line 383-5 to moderate salt stress (100 mM NaCl at day 10), identifying key lncRNA–mRNA regulatory networks. Salt stress induced pronounced, dose-dependent growth inhibition, oxidative damage, and osmotic adjustment, accompanied by extensive transcriptional reprogramming. Genome-wide analyses identified 6215 differentially expressed protein-coding genes and 941 salt-responsive long non-coding RNAs (lncRNAs), revealing coordinated regulation of ion transport, redox homeostasis, phytohormone signaling, and secondary metabolism. Functional enrichment analyses highlighted the central involvement of abscisic acid and ethylene signaling pathways, MAPK cascades, membrane transporters, and antioxidant systems. Notably, salt stress strongly activated the phenylpropanoid and lignin biosynthesis pathways, suggesting reinforced cell wall remodeling and enhanced oxidative stress mitigation. Integration of lncRNA–mRNA regulatory networks further indicated that non-coding transcripts act as important modulators linking hormone signaling, redox balance, and metabolic adaptation. Collectively, these results reveal a multilayered and tightly synchronized regulatory framework underlying salinity tolerance in B. napus and provide valuable molecular targets for the genetic improvement of salt-resilient rapeseed cultivars.