Leaf rust (Puccinia triticina Eriks) is a wheat disease causing substantial yield losses in wheat production globally. The identification of genetic resources with permanently effective resistance genes and the generation of mutant lines showing increased levels of resistance allow the efficient incorporation of these target genes into germplasm pools by marker-assisted breeding. In this study, new mutant (M₃ generation) lines generated from the rust-resistant variety Kazakhstanskaya-19 were developed using gamma-induced mutagenesis through 300-, 350-, and 400-Gy doses. In field trials after leaf rust inoculation, 75 mutant lines showed adult plant resistance. These lines were evaluated for resistance at the seedling stage via microscopy in greenhouse experiments. Most of these lines (89.33%) were characterized as resistant at both developmental stages. Hyperspectral imaging analysis indicated that infected leaves of wheat genotypes showed increased relative reflectance in visible and near-infrared light compared to the non-infected genotypes, with peak means at 462 and 644 nm, and 1936 and 2392 nm, respectively. Five spectral indexes, including red edge normalized difference vegetation index (RNDVI), structure-insensitive pigment index (SIPI), ratio vegetation index (RVSI), water index (WI), and normalized difference water index (NDWI), demonstrated significant potential for determining disease severity at the seedling stage. The most significant differences in reflectance between susceptible and resistant mutant lines appeared at 694.57 and 987.51 nm. The mutant lines developed were also used for the development and validation of KASP markers for leaf rust resistance genes Lr1, Lr2a, Lr3, Lr9, Lr10, and Lr17. The mutant lines had high frequencies of “a” resistance alleles (0.88) in all six Lr genes, which were significantly associated with seedling resistance and suggest the potential of favorable haplotype introgression through functional markers. Nine mutant lines characterized by the presence of “b” alleles in Lr9 and Lr10—except for one line with allele “a” in Lr9 and three mutant lines with allele “a” in Lr10—showed the progressive development of fungal haustorial mother cells 72 h after inoculation. One line from 300-Gy-dosed mutant germplasm with “b” alleles in Lr1, Lr2a, Lr10, and Lr17 and “a” alleles in Lr3 and Lr9 was characterized as resistant based on the low number of haustorial mother cells, suggesting the contribution of the “a” alleles of Lr3 and Lr9.

The increasing environmental challenges facing modern agriculture necessitate development of sustainable, eco-friendly alternatives to chemical inputs. This study aimed to isolate and characterize rhizophilic bacterial strains from the rhizosphere of the maize hybrid Turan 480 SV (Zea mays L.), with a focus on their plant growth-promoting and biocontrol traits. A total of 23 bacterial isolates were obtained, including 15 Gram-negative and 8 Gram-positive strains. Among these, three strains—CR14, CR18 and CR22—were selected for detailed analysis. All three demonstrated significant indole-3-acetic acid (IAA) production, phosphate and zinc solubilization, nitrogen fixation and antifungal activity. CR14 synthesized 56.01 mg L⁻¹ of IAA and demonstrated the highest zinc solubilization, while CR18 exhibited superior phosphate solubilization and protease activity. CR22 produced the highest IAA (61.46 mg L⁻¹) and demonstrated strong cellulase and amylase activity. In antagonism tests, CR14 suppressed Alternaria alternata with an 80 mm inhibition zone, while CR18 and CR22 effectively inhibited both A. alternata and Fusarium graminearum. Phylogenetic analysis based on 16S rRNA sequencing identified CR18 as Serratia quinivorans, CR14 as Pantoea agglomerans and CR22 as Pantoea sp. The functional diversity of rhizobacteria holds promise as bioinoculants for enhancing maize growth and protecting against soil-borne pathogens in sustainable agriculture.

Fusarium head blight, caused mainly by Fusarium graminearum is one of the most damaging diseases of wheat. Breeding durable disease resistance cultivars rely largely on continually introgression new resistance genes, especially the genes with different defense mechanisms, into adapted varieties. The main objective of this research was to evaluate three spring wheat cultivars grown in Kazakhstan and the mutant lines of spring wheat (M3 generations) developed on their genetic background by irradiation treatment (100 and 200 γ rays) for their resistance to Fusarium head blight disease and to use PCR-based DNA markers, such as SSRs markers to investigate genetic diversity in wheat germplasm. Significant differences in tolerance phenotype to Fusarium head blight were found among wheat cultivars and mutant lines. Comparing parent cv “Zhenis” M3 mutant lines, № 6(15), № 6(16) and 22(1) had the highest means of Fusarium resistance at 15-day after the inoculation. M3 mutant lines, №89(4) developed on base of cv. “Almaken” can be identified as FHB-tolerant. Three M3 mutant lines obtained on genetic background of cv. “Erithrospermum-35” №110(1), №129(3) and №150(5) had higher level of Fusarium tolerance then parent cultivar. A total of 21 SSRs loci were used to determine genetic diversity among M3 spring wheat lines and non-mutagenized plants

The increasing threat posed by wheat rust diseases caused by Puccinia spp. necessitates the development of resistance strategies that extend beyond conventional race-specific mechanisms. Although recent reviews (2023–2025) have emphasized gene discovery and genomic approaches, comparatively less attention has been given to the potential roles of metabolic regulation and micronutrient homeostasis in host–pathogen interactions. Here, we present a narrative synthesis of current evidence and propose a conceptual framework in which induced mutagenesis (ethyl methanesulfonate, EMS, and γ-irradiation) serves as a tool for investigating interactions among redox regulation, iron (Fe) homeostasis, and disease resistance. A key component of this framework is the proposed interplay between reactive oxygen species (ROS) signaling and Fe partitioning. Vacuolar iron transporters (VITs), ferritins, and associated transport networks regulate intracellular Fe distribution and may influence Fe availability at the host–pathogen interface, potentially affecting fungal development and host defense responses. This concept of “iron-withholding immunity” may operate alongside ROS-mediated defense processes, linking metabolism with immune function. Observations from mutant wheat populations are broadly consistent with the hypothesis that these processes may contribute to durable adult-plant resistance (APR), which is characterized by reduced disease development, coordinated defense responses, and relative stability across environments. In some studies, Fe-enriched mutant lines have been associated with enhanced expression of pathogenesis-related genes and the occurrence of combined APR and seedling-resistance phenotypes, suggesting possible links between micronutrient homeostasis and immunity. Integration of high-throughput phenotyping with genotype × environment × time (G × E × T) frameworks may further improve our understanding of quantitative resistance and disease-associated traits. Overall, this review highlights the potential importance of nutrient homeostasis, redox regulation, and susceptibility modulation as components of future research aimed at developing climate-resilient and nutritionally improved wheat cultivars.

Improving grain nutritional quality without reducing yield remains a major challenge in wheat breeding. This study aimed to identify advanced mutant lines of spring wheat with enhanced grain protein, iron (Fe), and zinc (Zn) contents combined with reduced phytate levels to improve mineral bioavailability. Mutant lines were developed from the spring wheat cultivar Zhenis using gamma irradiation (100 and 200 Gry) and evaluated for yield-related traits, grain morphometry, and nutritional parameters. Significant phenotypic and genetic variation was observed among the M₅ mutant lines. Grain protein content ranged from 13.23% to 15.63%, and 46.7% of the lines showed significantly higher protein levels than the parent cultivar. Likewise, 43.3% of the mutant lines showed increases in grain iron and zinc contents of up to 3.4- and 2.94-fold, respectively, compared to the control. Phytate-to-mineral molar ratios were significantly reduced, indicating improved mineral bioavailability. Correlation analysis revealed positive associations between micronutrient accumulation and grain morphometric traits, particularly grain area. No strong negative relationship between nutritional quality and yield-related traits was detected in the selected lines. These results demonstrate that gamma-induced mutagenesis is an effective approach for developing biofortified wheat genotypes with improved nutritional quality and stable agronomic performance.

In the context of global restrictions on the use of antibiotics in poultry farming, alternative approaches to disease prevention and productivity enhancement are of particular importance, among which probiotics occupy a leading place. The present study is aimed at screening and comprehensive characterization of Bacillusstrains with antagonistic and enzymatic activity for their further use as probiotic additives in poultry feed. As a result of isolation from samples of chicken manure, soil and gastric contents of chickens, isolates of spore-forming bacteria were obtained. Primary phenotypic selection included assessment of colony morphology and Gram staining. Antagonistic activity was assessed against 13 pathogenic microorganisms, including Escherichia coli, Salmonellaspp., Staphylococcus aureus, Proteusspp., Pseudomonas aeruginosaand Candida albicans. Based on the results of tests using the perpendicular streak and agar diffusion method, three most active strains were selected: P-1, Zh-2 and A-12. Strain A-12 also showed high proteolytic and cellulolytic activity. A Python script was used to quantitatively assess the enzymatic activity, allowing for a comparison of lysis zones and cellulose degradation levels. The safety of the strains was confirmed in vitro. Genotypic identification revealed a high degree of similarity with Bacillus subtilis. Due to the combination of antimicrobial and enzymatic properties, strain A-12 is a promising candidate for the development of a probiotic feed additive in poultry farming