Search Results (159)

Leymus chinensis (Trin.) Tzvel., a vital native forage grass in northern China for ecological restoration and livestock production, faces severe yield losses and grassland degradation due to rust (Puccinia spp.) infection. Current control strategies, reliant on chemical interventions, are limited by evolving resistance risks and environmental concerns, while rust-resistant breeding remains hindered by insufficient molecular insights. To address this, we systematically evaluated rust resistance in 24 L. chinensis germplasms from diverse geographic origins, identifying six highly resistant (HR) and five extremely susceptible (ES) genotypes. Integrating transcriptomics and metabolomics, we dissected molecular responses to Puccinia infection, focusing on contrasting HR (Lc71) and ES (Lc5) germplasms at 48 h post-inoculation. Transcriptomic analysis revealed 1012 differentially expressed genes (DEGs: 247 upregulated, 765 downregulated), with enrichment in cell wall biosynthesis and photosynthesis pathways but suppression of flavonoid synthesis. Metabolomic profiling identified 287 differentially accumulated metabolites (DAMs: 133 upregulated, 188 downregulated), showing significant downregulation of pterocarpans and flavonoids in HR germplasms, alongside upregulated cutin synthesis-related metabolites. Multi-omics integration uncovered 79 co-enriched pathways, pinpointing critical regulatory networks: (1) In the nucleotide metabolism pathway, genes Lc5Ns011910, Lc1Xm057211, and Lc4Xm043884 exhibited negative cor-relations with metabolites Deoxycytidine and Cytosine. (2) In flavonoid biosynthesis, Lc2Xm054924, Lc4Xm044161, novel.8850, Lc2Ns006303, and Lc7Ns021884 were linked to naringenin and naringenin-7-O-glucoside accumulation. These candidate genes likely orchestrate rust resistance mechanisms in L. chinensis. Our findings advance the molecular understanding of rust resistance and provide actionable targets for breeding resilient germplasms. Full article

Wheat leaf rust (Lr), caused by Puccinia triticina Eriks. (Pt), is one of the most important diseases affecting wheat production worldwide. Using resistant wheat cultivars is the most economic and environmentally friendly way to control leaf rust. The Chinese wheat cultivar Xinong1163-4 has shown good resistance to Lr in field trials. To identify the genetic basis of Lr resistance in Xinong1163-4, 195 recombinant inbred lines (RILs) from the Xinong1163-4/Thatcher cross were phenotyped for Lr severity in three environments: the 2017/2018, 2018/2019, and 2019/2020 growing seasons in Baoding, Hebei Province. Bulked segregant analysis and simple sequence repeat markers were then used to identify the quantitative trait loci (QTLs) for Lr adult plant resistance (APR) in the population. As a result, six QTLs were detected, designated as QLr.hbau-1BL.1, QLr.hbau-1BL.2, and QLr.hbau-1BL.3. These QTLs were predicted to be novel. QLr.hbau-4BL, QLr.hbau-4BL.1, and QLr.hbau-3A were identified at similar physical positions to previously reported QTLs. Based on chromosome positions and molecular marker testing, QLr.hbau-1BL.3 shares similar flanking markers with Lr46. Lr46 is a non-race-specific APR gene for leaf rust, stripe rust, and powdery mildew. Similarly, QLr.hebau-4BL showed resistance to multiple diseases, including leaf rust, stripe rust, Fusarium head blight, and powdery mildew. The QTLs identified in this study, as well as their closely linked markers, can potentially be used for marker-assisted selection in wheat breeding. Full article

Wheat (Triticum aestivum L.) is the world’s most indispensable staple crop and a vital source of food for human diet. Wheat stripe rust, caused by Puccinia striiformis f. sp. tritici (Pst), constitutes a severe threat to wheat production and in severe cases, the crop fails completely. Anmai1350 (AM1350) is moderately resistant to leaf rust and powdery mildew, and highly susceptible to sheath blight and fusarium head blight. We found that the length and area of mycelium in AM1350 cells varied at different time points of Pst infection. To investigate the molecular mechanism of AM1350 resistance to Pst, we performed transcriptome sequencing (RNA-seq). In this study, we analyzed the transcriptomic changes of the seedling leaves of AM1350 at different stages of Pst infection at 0 h post-infection (hpi), 6 hpi, 24 hpi, 48 hpi, 72 hpi, and 120 hpi through RNA-seq. Quantitative Real-Time Polymerase Chain Reaction (qRT-PCR) was used to validate RNA-seq data. It was determined that there were differences in the differentially expressed genes (DEGs) of AM1350, and the upregulation and downregulation of the DEGs changed with the time of infection. At different time points, there were varying degrees of enrichment in the response pathways of AM1350, such as the ”MAPK signaling pathway–plant”, the “plant–pathogen interaction” pathway and other pathways. After Pst infected AM1350, the reactive oxygen species (ROS) content gradually increases. The ROS is toxic to Pst, promotes the synthesis of phytoalexins, and inhibits the spread of Pst. As a result, AM1350 shows resistance to Pst race CYR34. The main objective of this study is to provide a better understanding for resistance mechanisms of wheat in response to Pst infections and to avoid production loss. Full article

Hybrid necrosis in wheat is caused by an interaction between two genes, Ne1 and Ne2, that triggers the gradual death of plant tissue. This trait affects wheat breeding as the gene Ne2 is the same as the gene Lr13 for leaf rust resistance. We have built a three-marker haplotype that consists of single nucleotide polymorphism (SNP) marker information already available on genotyping arrays for the determination of the presence and absence of Ne2. In this work, test crosses of eight bread wheat varieties with known and unknown Ne1 carriers showed that six of them possessed Ne2. We analyzed a set of wheat varieties which had partial SNPs and phenotypic data, i.e., hybrid necrosis and leaf rust reactions, using Kompetitive Allele-Specific PCR (KASP) markers previously available for Ne2. The observed haplotypes of the SNP markers RAC875_c1226_652, Ra_c4397_542, and AX-110926324 perfectly matched the KASP marker variants for Ne2 and ne2. A prediction, based on these SNP haplotypes, of the distribution of Ne2 in wheat varieties, predominantly from Germany and released between 1900 and 2024, showed that breeding steadily increased the proportion of Ne2 in the German gene pool. Full article

Leaf rust (LR) is a devastating foliar disease that impacts common wheat (Triticum aestivum L.) globally. For optimal disease protection, wheat cultivars should possess adult plant resistance (APR) to leaf rust. In the current study, the objective was to map quantitative trait loci (QTL) related to leaf rust resistance. This was achieved by using 193 recombinant inbred line (RIL) populations which were developed from the cross between N. Strampelli and Huixianhong. Four trials were conducted in China (three in Baoding, Hebei province, and one in Zhoukou, Henan province) to assesses the leaf rust response of the RILs and parental lines. The wheat 660K SNP array and additional SSR markers were used to genotype the RIL populations. Through inclusive composite interval mapping (ICIM), three QTL related to leaf rust (LR) resistance were detected. ICIM was also employed to reevaluate previously published data in order to identify QTL with pleiotropic effects. To determine the physical positions, the flanking sequences of all SNP probes were compared against the Chinese Spring wheat reference sequence through BLAST searches. Three leaf rust resistance loci, two on chromosome 2A and 5B, were contributed by N. Strampelli. QLr.hbau-2AL.1 was detected in three leaf rust environments with phenotypic variance explained (PVE of 12.2–17%); QLr.hbau-2AL.2 was detected in two environments with 12.5–13.2% of the PVE; and QLr.hbau-5BL was detected in all leaf rust environments with phenotypic variance explained (PVE) of 17.8–19.1%. QLr.hbau-5BL exhibited potentially pleiotropic responses to multiple diseases. The QTL and the associated flanking markers discovered in this study could prove valuable for purposes such as fine mapping, the exploration of candidate genes, and marker-assisted selection (MAS). Full article

Lesion mimic phenotypes, characterized by leaf spots formed in the absence of pathogens or pests, are often associated with reactive oxygen species (ROS) accumulation and cell necrosis. This study identified a novel and stable homozygous spotted phenotype (HSP) from the F₈ population of common wheat (XN509 × N07216). The yellow spots that appeared at the booting stage were light-sensitive, and accompanied by cell necrosis and H₂O₂ accumulation. Compared with homozygous normal plants (HNPs), HSPs exhibited enhanced resistance to stripe rust and powdery mildew without compromising yield. RNA-Seq analysis at three stages revealed that differentially expressed genes (DEGs) between HSPs and HNPs were significantly enriched in KEGG pathways related to photosynthesis and photosynthesis-antenna proteins. GO analysis highlighted chloroplast and light stimulus-related down-regulated DEGs. Fine mapping identified TaSpl1 within a 0.91 Mb interval on chromosome 3DS, flanked by the markers KASP188 and KASP229, using two segregating populations comprising 1117 individuals. The candidate region contained 42 annotated genes, including 14 DEGs based on previous BSR-Seq data. PCR amplification and qRT-PCR verification identified the expression of TraesCS3D02G022100 was consistent with RNA-Seq data. Gene homology analysis and silencing experiments confirmed that TraesCS3D02G022100 was associated with stay-green traits. These findings provide new insights into the genetic regulation of lesion mimics, photosynthesis, and disease resistance in wheat. Full article

Sugarcane rust diseases are caused by Puccinia melanocephala (brown rust) and Puccinia kuehnii (orange rust), and significantly threaten the sustainable and stable development of the global sugarcane industry. Erianthus arundinaceus within the Saccharum complex is a potential germplasm resource for sugarcane breeding and is characterized by its tolerance of infertile land, drought, and diseases. However, the research on resistance to rust in E. arundinaceus clones and their offspring (F1 and backcross with modern sugarcane varieties) is limited. In this study, a total of 201 leaf samples from Saccharum spp. hybrids with rust symptoms were collected and screened for disease occurrence. PCR detection revealed that 17.9% and 34.8% of the samples were infected by P. melanocephala and P. kuehnii, respectively. Additionally, 12.9% of the samples were infected by both pathogens. A total of 88 clones of E. arundinaceus offspring and the parents plus 3 additional E. arundinaceus were selected for the identification of brown rust resistance by an artificial inoculation method. Among them, 61 clones displayed high resistance to brown rust. Molecular detection showed that 13 offspring of E. arundinaceus and 6 backcross parents of the “ROC” series exhibited the major resistance gene (Bru1) for brown rust. Unexpectedly, the Bru1 gene was absent in 42 clones that were resistant to brown rust, suggesting that other resistance genes for brown rust likely exist in E. arundinaceus and their offspring. Our results offer some significant genetic resources for developing sugarcane cultivars with resistance against rust. Full article

Peanut rust, caused by Puccinia arachidis Speg., is one of the most significant leaf diseases globally, and has a severe impact on peanut yield and quality. The development of disease-resistant varieties is recognized as an effective strategy to mitigate the damage caused by peanut rust. However, the research foundation for understanding peanut rust remains relatively limited. In this study, we identified significant single nucleotide polymorphisms (SNPs) associated with peanut rust resistance using a natural population consisting of 353 peanut germplasm accessions. These accessions were analyzed based on resequencing data and rust disease phenotypes across one laboratory test and three field trials. A total of 18 significant SNPs were identified on chromosomes A05 (5 SNPs), A08 (7 SNPs), and A12 (6 SNPs). Notably, three SNPs—Arahy.05_93085395, Arahy.05_93114354, and Arahy.12_4097252—were consistently detected across multiple environments. Within their confidence intervals, 48 genes were annotated, including 9 NLR domain-containing genes functionally related to plant disease resistance, which may serve as candidate genes for peanut rust resistance. This study provides insights into the regulatory mechanisms underlying peanut rust resistance. Full article

In an effort to enhance wheat’s resilience against rust diseases, our research explores the genetic underpinnings of resistance in a diverse collection of winter bread wheat accessions. Leaf rust (Puccinia triticina), yellow rust (Puccinia striiformis f. sp. tritici), and stem rust (Puccinia graminis f. sp. tritici) are significant threats to global wheat production. By leveraging host genetic resistance, we can improve disease management strategies. Our study evaluated 55 wheat accessions, including germplasm from Kazakhstan, from Uzbekistan, from Russia, from Kyrgyzstan, France, and CIMMYT under field conditions in southern Kazakhstan from 2022 to 2024. The results showed a robust resistance profile: 49.1% of accessions exhibited high to moderate resistance to leaf rust, 12.7% to yellow rust, and 30.9% to stem rust. Notably, ten accessions demonstrated resistance to multiple rust species, while seven showed resistance to two rusts. Twenty accessions were selected for further seedling resistance and molecular analysis. Three accessions proved resistant to six isolates of P. triticina, two to four isolates of P. striiformis, and four to five isolates of P. graminis. Although no genotypes were found to be universally resistant to all rust species at the seedling stage, two accessions—Bezostaya 100 (Russia) and KIZ 90 (Kazakhstan)—displayed consistent resistance to leaf and stem rust in both seedling and field evaluations. Molecular analysis revealed the presence of key resistance genes, including Lr1, Lr3, Lr26, Lr34, Yr9, Yr18, Sr31, Sr57, and the 1AL.1RS translocation. This work provides valuable insights into the genetic landscape of wheat rust resistance and contributes to the development of new wheat cultivars that can withstand these diseases, enhancing global food security. Full article

Climate change is driving the spread of transboundary wheat diseases, necessitating the development of resilient wheat varieties for sustainable agriculture. Wheat rusts, including leaf rust (LR), yellow rust (YR), and stem rust (SR), remain among the most economically significant diseases, causing substantial yield losses worldwide. Enhancing genetic diversity by identifying and deploying rust resistance genes is crucial for durable resistance in wheat breeding programs. This study aimed to identify quantitative trait loci (QTL) associated with rust resistance in the CIMMYT wheat line Kasuku, released in Kenya in 2018. A recombinant inbred line (RIL) population (181 lines) derived from Kasuku (triple rust-resistant) and Apav#1 (triple rust-susceptible) was evaluated under artificial LR and YR epidemics in Mexico and YR and SR in Kenya. QTL mapping using genotyping-by-sequencing (DArTSeq) and phenotypic data identified four major loci: QLrYrSr.cim-1BL (Lr46/Yr29/Sr58) on 1BL, conferring resistance to LR, YR, and SR; QLrYr.cim-2AS (Yr17/Lr37) on 2AS, providing LR and YR resistance; QLrYr.cim-3AL on 3AL; and QLrYrSr.cim-6AL on 6AL, representing novel loci associated with multiple rust resistances. Additionally, minor QTL were also identified: for LR (QLr.cim-2DS on 2DS, QLr.cim-6DS on 6DS), for YR (QYrKen.cim-3DS on 3DS, QYrKen.cim-6BS on 6BS), and for SR (QSr.cim-2BS on 2BS, QSr.cim-5AL on 5AL, QSr.cim-6AS on 6AS). RILs carrying these QTL combinations exhibited significant reductions in rust severity. Flanking markers for these loci are being used to develop Kompetitive Allele-Specific PCR (KASP) markers for fine mapping and marker-assisted selection (MAS). These findings contribute to the strategic deployment of rust resistance genes in wheat breeding programs, facilitating durable resistance to multiple rust pathogens. Full article

The application of marker-assisted selection in coffee breeding programs accelerates the identification and concentration of target alleles, being essential for developing cultivars resistant to multiple diseases. In this study, a population was developed from artificial crossings between Timor Hybrid and Tupi Amarelo, with the aim of promoting the pyramiding of resistance genes to the main diseases and pests of Coffea arabica: coffee leaf rust (CLR), coffee berry disease (CBD), cercospora, and leaf miner. Resistance was confirmed by nine molecular markers at loci associated with CLR (genes SH3, CC-NBS-LRR, RLK, QTL-GL2, and GL5) and with CBD (gene Ck-1). The resistance to CLR, cercospora, and leaf miner was evaluated using phenotypic diagrammatic scales. Mixed models estimated population superiority in 16 morphoagronomic traits over four agricultural years. The introgression of resistance alleles to CLR and CBD was identified in 98.6% of the population, with 29% showing pyramiding of five resistance genes. These pyramiding genotypes showed 100% resistance to the leaf miner and 90% to cercospora. The traits were grouped into univariate, bivariate, and trivariate repeatability models, with 11 significant ones. These results are indicative of genetic variability to be explored in the development of cultivars with multiple resistances and high agronomic potential. Full article

Wheat leaf rust caused by Puccinia triticina (Pt) is a prevalent disease worldwide, seriously threatening wheat production. Pt acquires nutrients from host cells via haustoria and secretes effector proteins to modify and regulate the expression of host disease resistance genes, thereby facilitating pathogen growth and reproduction. The study of effector proteins is of great significance for clarifying the pathogenic mechanisms of Pt and effective control of leaf rust. Herein, we report a wheat leaf rust candidate effector protein Pt48115 that is highly expressed in the late stages of infection during wheat–Pt interaction. Pt48115 contains a signal peptide with a secretory function and a transit peptide that can translocate Pt48115 to the host chloroplasts. The amino acid sequence polymorphism analysis of Pt48115 in seven different leaf rust races showed that it was highly conserved. Pt48115 inhibited cell death induced by Bcl-2-associated X protein (BAX) from mice or infestans 1 (INF1) from Phytophthora infestans in Nicotiana benthamiana and by DC3000 in wheat, and its 145–175 amino acids of the C-terminal are critical for its function. Furthermore, Pt48115 inhibited callose deposition and reactive oxygen species accumulation in the wheat cultivar Thatcher, demonstrating that it is an effector that enhances Pt virulence by suppressing wheat defense responses. Our findings lay a foundation for future studies on the pathogenesis of Pt during wheat–fungus interaction. Full article

The main diseases that affect coffee production worldwide are coffee leaf rust (CLR) and coffee berry disease (CBD), caused by fungi Hemileia vastatrix and Colletotrichum kahawae, respectively. The identification of cultivars with stacking resistance genes is of paramount importance for the control of these diseases. This work aimed to profile the phenotypic and genetic resistance of 160 genotypes belonging to 36 commercial coffee cultivars from five Central American countries regarding resistance to races II and XXXIII of H. vastatrix through phenotypic evaluation and evaluations associated with the genetic loci of resistance to CLR and CBD by molecular markers. Of the 160 genotypes from Central America evaluated, 26.25% presented genes stacked to the three loci of resistance to CLR and the locus of resistance to CBD, and resistance to races II and XXXIII when inoculated with urediniospores. In addition, 14 genotypes were identified with the presence of the S_H3 gene, whose resistance has not yet been broken. This work revealed errors in passport data or hybridizations in cultivars and even possible resistance breakdown in the Catimor genetic group. These results are essential to the search for strategies in coffee genetic breeding programs. Full article

The fungus Puccinia triticina Eriks (Pt) is the cause of leaf rust, one of the most damaging diseases, which significantly reduces common wheat yields. In Pt-resistant adult plants, an APR-type resistance is observed, which protects the plant against multiple pathogen races and is distinguished by its persistence under production conditions. With a more complete understanding of the molecular mechanisms underlying the function of APR genes, it will be possible to develop new strategies for resistance breeding in wheat. Currently, mainly APR genes, such as Lr34, Lr46, and Lr67, are principally involved in resistance breeding as they confer durable resistance to multiple fungal races occurring under different climatic and environmental conditions. However, the mechanisms underlying the defence against pathogens mediated by APR genes remain largely unknown. Our research aimed to shed light on the molecular mechanisms related to resistance genes and miRNAs expression, underlying APR resistance to leaf rust caused by Pt. Furthermore, the present study aimed to identify and functionally characterize the investigated miRNAs and their target genes in wheat in response to leaf rust inoculation. The plant material included hybrid forms of wheat from the F₂ and BC₁F₁ generations, obtained by crossing the resistance cultivar Glenlea (CItr 17272) with agriculturally important Polish wheat cultivars. Biotic stress was induced in adult plants via inoculation with Pt fungal spores under controlled conditions. The RT-qPCR method was used to analyze the expression profiles of selected APR genes at five time points (0, 6, 12, 24, and 48 hpi). The results presented here demonstrate the differential expression of APR genes and miRNAs at stages of leaf rust development at selected timepoints after inoculation. We analyzed the expression of three leaf rust resistance genes, using different genetic backgrounds in F₂ and BC₁F₁ segregation materials, in leaf tissues after Pt infection. Our goal was to investigate potential differences resulting from the genetic background found in different generations of hybrid forms of the same parental forms. Gene ontology analysis predicted 190 target genes for tae-miR5384-3p and 167 target genes for tae-miR9653b. Our findings revealed distinct expression profiles for genes, with the highest expression levels observed mainly at 6, 24, and 48 hpi. The candidate gene Lr46-Glu2 displayed an upregulation, suggesting its potential involvement in the immune response against Pt infection. Full article

Soybean (Glycine max (L.) Merr.) is one of the most profitable crops among the legumes grown worldwide. The occurrence of rust epidemics, caused by Phakopsora pachyrhizi, has greatly contributed to yield losses and an abusive use of fungicides. Within this context, this study investigated the potential of using a phosphite of nickel (Ni) and potassium (K) [referred to as induced resistance (IR) stimulus] to induce soybean resistance against infection by P. pachyrhizi. Plants were sprayed with water (control) or with IR stimulus and non-inoculated or inoculated with P. pachyrhizi. The germination of urediniospores was greatly reduced in vitro by 99% using IR stimulus rates ranging from 2 to 15 mL/L. Rust severity was significantly reduced from 68 to 78% from 7 to 15 days after inoculation (dai). The area under the disease progress curve significantly decreased by 74% for IR stimulus-sprayed plants compared to water-sprayed plants. For inoculated plants, foliar concentrations of K and Ni were significantly higher for IR stimulus treatment than for the control treatment. Infected and IR stimulus-sprayed plants had their photosynthetic apparatus (a great pool of photosynthetic pigments, and lower values for some chlorophyll a fluorescence parameters) preserved, associated with less cellular damage (lower concentrations of malondialdehyde, hydrogen peroxide, and anion superoxide) and a greater production of phenolics and lignin than plants from the control treatment. In response to infection by P. pachyrhizi, defense-related genes (PAL2.1, PAL3.1, CHIB1, LOX7, PR-1A, PR10, ICS1, ICS2, JAR, ETR1, ACS, ACO, and OPR3) were up-regulated from 7 to 15 dai for IR stimulus-sprayed plants in contrast to plants from the control treatment. Collectively, these findings provide a global picture of the enhanced capacity of IR stimulus-sprayed plants to efficiently cope with fungal infection at both biochemical and physiological levels. The direct effect of this IR stimulus against urediniospores’ germination over the leaf surface needs to be considered with the aim of reducing rust severity. Full article