The fungal pathogen Puccinia striiformis f. sp. tritici, which causes yellow rust disease, poses a significant economic threat to wheat production not only in Uzbekistan but also globally, leading to substantial reductions in grain yield. This study aimed to develop yellow rust-resistance wheat lines by introgressing Yr10 and Yr15 genes into high-yielding cultivar Grom using the marker-assisted backcrossing (MABC) method. Grom was crossed with donor genotypes Yr10/6*Avocet S and Yr15/6*Avocet S, resulting in the development of F₁ generations. In the following years, the F₁ hybrids were advanced to the BC₂F₁ and BC₂F₂ generations using the MABC approach. Foreground and background selection using microsatellite markers (Xpsp3000 and Barc008) were employed to identify homozygous Yr10- and Yr15-containing genotypes. The resulting BC₂F₂ lines, designated as Grom-Yr10 and Grom-Yr15, retained key agronomic traits of the recurrent parent cv. Grom, such as spike length (13.0–11.9 cm) and spike weight (3.23–2.92 g). Under artificial infection conditions, the selected lines showed complete resistance to yellow rust (infection type 0). The most promising BC₂F₂ plants were subsequently advanced to homozygous BC₂F₃ lines harboring the introgressed resistance genes through marker-assisted selection. This study demonstrates the effectiveness of integrating molecular marker-assisted selection with conventional breeding methods to enhance disease resistance while preserving high-yielding traits. The newly developed lines offer valuable material for future wheat improvement and contribute to sustainable agriculture and food security.

Enhancing plants’ resistance against FW is crucial for ensuring a sustainable global chickpea production. The present study focuses on the identification of fungal pathogens and the assessment of ninety-six chickpea samples for Fusarium wilt from the International Center for Agricultural Research in the Dry Areas (ICARDA)’s collection. Eight fungal isolates were recovered from the symptomatic chickpeas. Polyphasic identification was conducted by comparing the internal transcribed spacer region (ITS), the elongation factor 1-α (tef1-α), and beta-tubulin (tub2). Among them, Neocosmospora solani, N. nelsonii, N. falciformis, N. brevis, Fusarium brachygibbosum, and F. gossypinum were identified. An analysis of the genetic diversity of chickpeas, using 69 polymorphic simple sequence repeat (SSR) markers, revealed a total of 191 alleles across all markers, with, on average, each SSR marker detecting approximately 2.8 alleles. A STRUCTURE analysis delineated lines into two distinct sub-groups (K = 2). Association mapping, using the generalized linear model (GLM) and mixed linear model (MLM) approaches, identified six and five marker–trait associations (MTAs) for FW resistance, respectively. Notably, these TA42, TA125 (A) and TA125 (B), TA37, and TAASH MTAs, commonly found in both models, emerge as potential candidates for the targeted enhancement of FW resistance in chickpeas. To our knowledge, this study represents an inaugural report on the association mapping of genomic loci governing FW resistance in chickpeas from the ICARDA’s accessions.

Plant-associated bacteria play a crucial role in protecting plants from pathogens, yet the diversity and antagonistic potential of these bacteria across different plant species remain underexplored, especially in central Asia. To investigate the competitive dynamics between phytopathogenic fungi and plant-associated bacteria, we collected stem and root samples from 50 plant species across nine regions of Uzbekistan. A total of 3355 bacterial isolates were obtained (1896 from roots and 1459 from shoots) and screened for antifungal activity against six fungal pathogens, resulting in 432 antagonistic isolates. These were identified through 16S rDNA sequencing, revealing 65 bacterial species across three phyla: Firmicutes, Proteobacteria, and Actinobacteria, predominantly in the respective families Bacillaceae, Pseudomonadaceae, and Caryophanaceae. The plant Salsola vvedenskii hosted the highest diversity of antagonists (26 species), while other species harbored fewer. Plant species showed strong associations with specific bacterial communities, with 14 plant species each hosting unique antagonists. Enzymatic profiling revealed functional diversity, with Bacillus species producing protease, cellulase, and lipase activities, while Pseudomonas species excelled in xylanase, glucanase, and cellobiase production. B. mojavensis 9r-29 stood out by producing all six enzymes. These findings underscore the ecological diversity and biocontrol potential of plant-associated bacteria in natural ecosystems, offering promising candidates for sustainable plant protection strategies.

In this study, molecular markers were employed to determine the resistance of wheat varieties to yellow rust. Resistant isogenic lines of Avocet were crossed with high-yielding varieties, and the resulting backcross generations were evaluated both phenotypically and genotypically. The research findings confirmed that SSR markers Xpsp3000 and Barc008 are closel linked to the resistance genes Yr10 and Yr15, respectively. These results demonstrated that the application of marker-assisted selection (MAS) technology in the breeding process is an effective approach for developing new varieties resistant to yellow rust.

Endophytic fungi were isolated from healthy vegetative organs (leaves, roots and stems) of the invasive plant Xanthium strumarium L. harvested from 3 regions of Uzbekistan. This study aimed to characterise the molecular diversity of endophytic fungi associated with this invasive species. Fungal identification was performed using internal transcribed spacer ribosomal DNA (ITS rDNA) sequencing followed by Basic Local Alignment Search Tool (BLAST) analysis against GenBank and MycoBank databases. A total of 361 isolates were grouped into 36 operational taxonomic units (OTUs), representing 20 fungal genera. Leaves harboured the highest proportion of isolates (53.19 %), followed by roots and stems. The genus Alternaria, particularly Alternaria alstroemeriae, was the dominant taxon, while Fusarium species were also frequently detected. Several OTUs exhibited relatively low sequence similarity to reference sequences, indicating the presence of genetically distinct taxa. This study provides the first molecular insight into the diversity of endophytic fungi associated with X. strumarium populations in Uzbekistan and highlights their potential ecological significance.