New Sources Of Resistance Research Articles

Survey of Heterodera glycines Population Abundance and Virulence Phenotypes During 2021 to 2022 in Heilongjiang Province.

Soybean cyst nematode (SCN), Heterodera glycines, poses a significant threat to global soybean production. Heilongjiang, the largest soybean-producing province in China, contributes more than 40% to the country's total yield. This province has much longer history of SCN infestation. To assess the current situation in Heilongjiang, we conducted a survey to determine the SCN population density and virulence phenotypes during 2021 to 2022 and compared the data with a previous study in 2015. A total of 377 soil samples from 48 counties representing 11 major soybean-planting regions were collected. The prevalence of SCN increased from 55.4% in 2015 to 59% in the current survey. The population densities ranged from 80 to 26,700 eggs and juveniles per 100 cm3 of soil. Virulence phenotypes were evaluated for 60 representative SCN populations using the H. glycines (HG) type test, revealing nine different HG types. The most common virulence phenotypes were HG types 7 and 0, accounting for 56.7 and 20% of all SCN populations, respectively. The prevalence of populations with a female index (FI) greater than 10% on PI 548316 increased from 64.5% in 2015 to 71.7%. However, the FI on the commonly used resistance sources PI 548402 (Peking) and PI 437654 remained low at 3.3%. These findings highlight the increasing prevalence and changing virulence phenotypes of SCN in Heilongjiang. They also emphasize the importance of rotating soybean varieties with different resistance sources and urgently identifying new sources of resistance to combat SCN.

Identification of Sources of Resistance to Aphanomyces Root Rot in Pisum.

Aphanomyces root rot (ARR), caused by Aphanomyces euteiches, is one of the most devastating diseases that affect the production of peas. Several control strategies such as crop rotation, biocontrol, and fungicides have been proposed, but none provides a complete solution. Therefore, the deployment of resistant cultivars is fundamental. ARR resistance breeding is hampered by the moderate levels of resistance identified so far. The available screening protocols require post-inoculation root assessment, which is destructive, time-consuming, and tedious. In an attempt to address these limitations, we developed a non-destructive screening protocol based on foliar symptoms and used it to identify new sources of resistance in a Pisum spp. germplasm collection. Accessions were root inoculated separately with two A. euteiches isolates, and leaf symptoms were assessed at 5, 10, 14, 17, and 20 days after inoculation (DAI). Although the majority of accessions exhibited high levels of susceptibility, thirty of them exhibited moderate resistance. These thirty accessions were selected for a second experiment, in which they were inoculated with both A. euteiches isolates at two inoculum doses. The objective of this second trial was to confirm the resistance of these accessions by evaluating root and biomass loss, as well as foliar symptoms, and to compare root and foliar evaluations. As a result, a high correlation (R2 = 0.75) between foliar and root evaluations was observed, validating the foliar evaluation method. Notably, accessions from P.s. subsp. humile exhibited the lowest symptomatology across all evaluation methods, representing valuable genetic resources for breeding programs aimed at developing pea varieties resistant to ARR.

Fine mapping of stem rust resistance derived from soft red winter wheat cultivar AGS2000 to an NLR gene cluster on chromosome 6D

The Puccinia graminis f. sp. tritici (Pgt) Ug99-emerging virulent races present a major challenge to global wheat production. To meet present and future needs, new sources of resistance must be found. Identification of markers that allow tracking of resistance genes is needed for deployment strategies to combat highly virulent pathogen races. Field evaluation of a DH population located a QTL for stem rust (Sr) resistance, QSr.nc-6D from the breeding line MD01W28-08-11 to the distal region of chromosome arm 6DS where Sr resistance genes Sr42, SrCad, and SrTmp have been identified. A locus for seedling resistance to Pgt race TTKSK was identified in a DH population and an RIL population derived from the cross AGS2000 × LA95135. The resistant cultivar AGS2000 is in the pedigree of MD01W28-08-11 and our results suggest that it is the source of Sr resistance in this breeding line. We exploited published markers and exome capture data to enrich marker density in a 10 Mb region flanking QSr.nc-6D. Our fine mapping in heterozygous inbred families identified three markers co-segregating with resistance and delimited QSr.nc-6D to a 1.3 Mb region. We further exploited information from other genome assemblies and identified collinear regions of 6DS harboring clusters of NLR genes. Evaluation of KASP assays corresponding to our co-segregating SNP suggests that they can be used to track this Sr resistance in breeding programs. However, our results also underscore the challenges posed in identifying genes underlying resistance in such complex regions in the absence of genome sequence from the resistant genotypes.

Identification of new sources of resistance against late leaf spot disease of groundnut using molecular and field screenings

ABSTRACT Late leaf spot (LLS), caused by the fungus Nothopassalora personata, is an important foliar disease in groundnut (Arachis hypogaea L.) production. The present study used previously reported three single nucleotide polymorphism (SNP) markers to screen a set of groundnut germplasm and compared them with phenotypic values of three hotspot locations. The results indicated that marker-identified genotypes had LLS-resistant or moderately resistant phenotypes. About 56% of the phenotypically confirmed genotypes were confirmed with the SNP genotype. Some of the phenotypically resistant genotypes were not confirmed with marker genotypes, indicating some other quantitative trait locus (QTL) responsible for the LLS resistance might have been involved. The findings in this study are relevant to future LLS resistance breeding programs.

Association mapping of tan spot and septoria nodorum blotch resistance in cultivated emmer wheat.

A total of 65 SNPs associated with resistance to tan spot and septoria nodorum blotch were identified in a panel of 180 cultivated emmer accessions through association mapping Tan spot and septoria nodorum blotch (SNB) are foliar diseases caused by the respective fungal pathogens Pyrenophora tritici-repentis and Parastagonospora nodorum that affect global wheat production. To find new sources of resistance, we evaluated a panel of 180 cultivated emmer wheat (Triticum turgidum ssp. dicoccum) accessions for reactions to four P. tritici-repentis isolates Pti2, 86-124, 331-9 and DW5, two P. nodorum isolate, Sn4 and Sn2000, and four necrotrophic effectors (NEs) produced by the pathogens. About 8-36% of the accessions exhibited resistance to the four P. tritici-repentis isolates, with five accessions demonstrating resistance to all isolates. For SNB, 64% accessions showed resistance to Sn4, 43% to Sn2000 and 36% to both isolates, with Spain (11% accessions) as the most common origin of resistance. To understand the genetic basis of resistance, association mapping was performed using SNP (single nucleotide polymorphism) markers generated by genotype-by-sequencing and the 9K SNP Infinium array. A total of 46 SNPs were significantly associated with tan spot and 19 SNPs with SNB resistance or susceptibility. Six trait loci on chromosome arms 1BL, 3BL, 4AL (2), 6BL and 7AL conferred resistance to two or more isolates. Known NE sensitivity genes for disease development were undetected except Snn5 for Sn2000, suggesting novel genetic factors are controlling host-pathogen interaction in cultivated emmer. The emmer accessions with the highest levels of resistance to the six pathogen isolates (e.g., CItr 14133-1, PI 94634-1 and PI 377672) could serve as donors for tan spot and SNB resistance in wheat breeding programs.

Search for sources of resistance to leaf diseases among present winter bread wheat varieties in the southern part of the Rostov region

The purpose of the current work was to search for sources of winter wheat varieties’ resistance to the most common pathogens of the area under artificial infectious backgrounds and recommend them for inclusion in the breeding process. The study was carried out on the experimental plots of the laboratory for plant immunity and protection of the FSBSI Agricultural Research Center “Donskoy” in 2021–2023. In order to expand the genetic diversity in immunity of newly developed varieties, it is necessary to use new sources of resistance. The objects of study were 78 winter wheat varieties from interstation variety testing, representing various breeding institutions in Russia and some foreign varieties. The study material was presented by the North Caucasian populations of pathogens of such wheat leaf diseases as powdery mildew, brown and yellow rust, and leaf spot (Septoria). Infectious backgrounds were formed according to generally accepted methods, using spore material of pathogens both stored and collected from crops in the previous year (types of rust) and collected from overwintered plants in the spring (powdery mildew, leaf spot). Weather conditions varied across the years of study (mainly in the autumn), but the damage to susceptible test varieties in the experiments was maximum. As a result of the study of the varieties on their resistance to one pathogen, there have been identified 23 varieties resistant to powdery mildew, 56 ones to leaf rust, 47 ones to yellow rust, 8 varieties to leaf spot. There has been given a characteristic of varieties according to various degree of resistance or susceptibility to each pathogen. On the resistance to two pathogens, there have been identified 17 varieties resistant to brown and yellow rust, 2 varieties resistant to brown rust and powdery mildew, 2 varieties resistant to yellow rust and powdery mildew, 1 variety resistant to brown rust and leaf spot. Ten varieties have shown resistance to no one pathogen, but they have had moderate resistance or moderate susceptibility to several other pathogens. 20 varieties were resistant to three diseases in various combinations, and 16 of them were resistant to brown, yellow rust, and powdery mildew. One variety ‘MV Nador’ from Hungary showed resistance to all 4 pathogens. All resistant varieties identified in the study can replenish the supply of winter wheat sources to the complex of leaf diseases for breeding purposes or be used in integrated crop protection against leaf diseases.

Genome wide association study of seedling and adult plant leaf rust resistance in two subsets of barley genetic resources

Leaf rust (LR) caused by Puccinia hordei is a serious disease of barley worldwide, causing significant yield losses and reduced grain quality. Discovery and incorporation of new sources of resistance from gene bank accessions into barley breeding programs is essential for the development of leaf rust resistant varieties. To identify Quantitative Trait Loci (QTL) conferring LR resistance in the two barley subsets, the Generation Challenge Program (GCP) reference set of 142 accessions and the leaf rust subset constructed using the Focused Identification of Germplasm Strategy (FIGS) of 76 barley accessions, were genotyped to conduct a genome-wide association study (GWAS). The results revealed a total of 59 QTL in the 218 accessions phenotyped against barley leaf rust at the seedling stage using two P. hordei isolates (ISO-SAT and ISO-MRC), and at the adult plant stage in four environments in Morocco. Out of these 59 QTL, 10 QTL were associated with the seedling resistance (SR) and 49 QTL were associated with the adult plant resistance (APR). Four QTL showed stable effects in at least two environments for APR, whereas two common QTL associated with SR and APR were detected on chromosomes 2H and 7H. Furthermore, 39 QTL identified in this study were potentially novel. Interestingly, the sequences of 27 SNP markers encoded the candidate genes (CGs) with predicted protein functions in plant disease resistance. These results will provide new perspectives on the diversity of leaf rust resistance loci for fine mapping, isolation of resistance genes, and for marker-assisted selection for the LR resistance in barley breeding programs worldwide.

Management and breeding for rust resistance in legumes

AbstractRust diseases are a major concern in legume production worldwide causing heavy losses especially in developing countries that depend on grain legumes as staple food. Fungal species from Uromyces, Phakopsora and Puccinia genera are the main causal agents of the various legume rust diseases. They induce up to 100% yield losses on susceptible cultivars and are emerging as a substantial threat to global food security. Developing durable resistance to rust has thus become a critical breeding objective alongside efforts to improve cultural and disease management practices. This review specifically focuses on the recent advances in understanding and enhancing genetic rust resistance across diverse legume crops. Key topics covered include: (i) the diversity and host range of the rust species affecting legumes; (ii) the disease management strategies from cultural practices to chemical control; (iii) the available screening methods for identifying new sources of resistance; (iv) the genetic basis of resistance, encompassing both major resistance genes and quantitative trait loci; (v) insights into gene regulation and effector molecules leading to legume-rust interactions; and (vi) emerging genomic-assisted breeding techniques that can accelerate the development of durable rust resistance in legumes. Overall, this review highlights the progress made to date and the remaining challenges in sustainably managing rust diseases across diverse legume crops through integrated approaches spanning pathogen biology, advanced phenotyping, genetic resistance, and molecular breeding.

Exploring the source of TYLCV resistance in Nicotiana benthamiana.

Tomato Yellow Leaf Curl Virus (TYLCV) is one of the most devastating pathogens of tomato, worldwide. It is vectored by the globally prevalent whitefly, Bemisia tabaci, and is asymptomatic in a wide range of plant species that act as a virus reservoir. The most successful crop protection for tomato in the field has been from resistance genes, of which five loci have been introgressed fromwild relatives. Of these, the Ty-1/Ty-3 locus, which encodes an RNA-dependent RNA polymerase 3 (RDR3), has been the most effective. Nevertheless, several TYLCV strains that break this resistance are beginning to emerge, increasing the need for new sources of resistance. Here we use segregation analysis and CRISPR-mediated gene dysfunctionalisation to dissect the differential response of two isolates of Nicotiana benthamiana to TYLCV infection. Our study indicates the presence of a novel non-RDR3, but yet to be identified, TYLCV resistance gene in a wild accession of N. benthamiana. This gene has the potential to be incorporated into tomatoes.

Characterisation and mapping of a Globodera pallida resistance derived from the wild potato species Solanum spegazzinii

Key messageA new resistance locus acting against the potato cyst nematode Globodera pallida was mapped to chromosome VI in the diploid wild potato species Solanum spegazzinii CPC 7195.The potato cyst nematodes (PCN) Globodera pallida and Globodera rostochiensis are economically important potato pests in almost all regions where potato is grown. One important management strategy involves deployment through introgression breeding into modern cultivars of new sources of naturally occurring resistance from wild potato species. We describe a new source of resistance to G. pallida from wild potato germplasm. The diploid species Solanum spegazzinii Bitter accession CPC 7195 shows resistance to G. pallida pathotypes Pa1 and Pa2/3. A cross and first backcross of S. spegazzinii with Solanum tuberosum Group Phureja cultivar Mayan Gold were performed, and the level of resistance to G. pallida Pa2/3 was determined in progeny clones. Bulk-segregant analysis (BSA) using generic mapping enrichment sequencing (GenSeq) and genotyping-by-sequencing were performed to identify single-nucleotide polymorphisms (SNPs) that are genetically linked to the resistance, using S. tuberosum Group Phureja clone DM1-3 516 R44 as a reference genome. These SNPs were converted into allele-specific PCR assays, and the resistance was mapped to an interval of roughly 118 kb on chromosome VI. This newly identified resistance, which we call Gpa VIlspg, can be used in future efforts to produce modern cultivars with enhanced and broad-spectrum resistances to the major pests and pathogens of potato.

Mutagenesis-Derived Resistance to Black Point in Wheat.

Black point, a severe global wheat disease, necessitates deploying resistant cultivars for effective control. However, susceptibility remains prevalent among most wheat cultivars. Identifying new sources of resistance and understanding their mechanisms are crucial for breeding resistant cultivars. This study pinpointed black point resistance in an ethyl methane sulfonate (EMS)-mutagenized wheat population of Wanyuanbai 1 (WYB) and analyzed resistant mutants using RNA-Seq. The findings revealed the following: (i) wyb-18, among 10,008 EMS-mutagenized lines, exhibited robust resistance with significantly lower black point incidence under artificial Bipolaris sorokiniana inoculation in 2020 and 2021 (average incidence of 5.2% over 2 years), markedly reduced compared with WYB (50.9%). (ii) wyb-18 kernels displayed black point symptoms at 12 days after inoculation (dai), 3 days later than WYB. At 15 dai, wyb-18 kernels had isolated black spots, unlike WYB kernels, where the entire embryo turned black. (iii) wyb-18 showed heightened antioxidant enzyme activity, including peroxidase, catalase, and superoxide dismutase. (iv) Analysis of 543 differentially expressed genes between wyb-18 and WYB at 9 dai identified enrichment in the MAPK signaling pathway through KEGG analysis. Ten genes in this pathway exhibited upregulated expression, while one was downregulated in wyb-18. Among these genes, PR1, WRKY11, SAPK5, and TraesCS1A02G326800 (chitin recognition protein) consistently showed upregulation in wyb-18, making them potential candidates for black point resistance. These results offer valuable germplasm resources for breeding and novel insights into the mechanisms of black point resistance.

Genetic diversity and heritability of tomato parental lines assembled for Ralstonia solanacearum resistance

Bacterial wilt is a disease caused by Ralstonia solanacearum, which affects over 450 plant species and causes significant reduction in crop yields including of tomato (Solanum lycopersicum) worldwide. Developing and identifying tomato genotypes with Ralstonia solanacearum tolerance and high yield potential, presents an opportunity for improvement of crop productivity. The objective of this study was to explore the heritability of tomato resistance against bacterial wilt and the genetic variation within the population for breeding purposes. A breeding population was created by crossing two bacterial wilt-resistant (MT56 and BL333) and three commercially desirable susceptible (Assila, Rambo and Heinz) tomato varieties, using North Carolina Design II, in a screen house at the Makerere University Agricultural Research Institute, Kabanyolo (MUARIK). Results showed that the Area Under Disease Progress Curve was significant (P<0.001), indicating that cumulative disease progress was less in resistant genotypes of segregating generations. Disease severity increased with days after inoculation (DAI), with Heinz showing the highest level of susceptibility. The General Combining Ability for male parent (GCAm) was significant (P< 0.01), and Specific Combining Ability (SCAf×m) and GCAf were significant (P<0.01) for the F2 generation. Broad-sense heritability was higher than the narrow-sense heritability in both F1 and F2 generations, suggesting that non-additive gene action predominately controlled tomato resistance to bacterial wilt infestation. The genetic diversity ranged from 0.5 to 0.6759, with a mean value of 0.5787. Polymorphism Information Content (PIC) varied from 0.375 to 0.6357, with a mean of 0.4888, indicating a high degree of variation. SLM 12-2 was the most polymorphic marker, with a PIC of 0.6357. The Unweighted Pair-Group Method with Arithmetic Average (UPGMA) classified all tomato genotypes into six clusters, namely Clusters 1 and 2 (Susceptible parents), Cluster 3 (Resistant parents), Clusters 4 and 5 (New source of resistance), and Cluster 6 (F1P1×P5).

Identification of sources of resistance among potato breeding material against stem nematode

Goal. To identify new sources of resistance against stem nematode among potato breeding material and provide recommendations for the involvement of the most promising genotypes in breeding practice.
 Methods. The research was conducted in the breeding laboratory of the Polissia Research Department of the Institute for Potato Research, during 2018—2022, with promising source material of its own potato breeding, interspecific hybrids of the laboratory of genetic resources of the Institute for Potato Research and potato varieties and studied their resistance to stem nematode on an infectious background.
 Results. It was found that among the studied hybrid potato material, up to 9% of highly resistant forms, about 15—29% with relatively high and 41—62% of genotypes with moderate resistance were distinguished. Among the evaluated potato varieties, only a small number demonstrate high resistance, while the majority exhibit moderate resistance to the nematode. Sources with high, relatively high and moderate resistance to the nematode among promising potato hybrids were identified. Selected genotypes are the following: G.10.7/13, P.14.17-14, P.15.5/27, G.09.8-14, Z.14.64/3, P.13.26/13, G.08.194/122, Z.14.64-2, G.15.1-3, Z.14.49-7 and P.14.43-18 combine resistance to stem nematode with high expression of the main economically valuable traits. It was found that the breeding material that showed moderate resistance to the nematode was created with the participation of potato varieties: Santarka, Radomysl, Irbytskyi, Podoliia, Bellarossa, Satina, Tyras, Vektar and Hurman. As a result of targeted breeding work, three new potato varieties have been created: Fanatka, Rostavytsia and Dzhavelina, characterised by high productivity, drought tolerance, and resistance to stem nematode and quarantine microorganisms.
 Conclusions. We recommend using the selected stem nematode-resistant hybrids in breeding work to develop resistant potato varieties. To limit the spread and development of the nematode, we recommend cultivating the suggested resistant potato varieties.

Screening of wild Ipomoea genotypes for resistance against sweet potato weevil Cylas formicarius F. based on multiple choice bioassay and phytochemical constituents

Screening of wild Ipomoea sp. and identification of new sources of resistance to the sweet potato weevil (Cylas formicarius Fabricius) with I. palmata, I. mauritiana, I. obscura, I. triloba were carried out. The leaves, vines and tubers of the different Ipomoea sp. were screened using multiple choice bioassay. The insect feeding holes on I. mauritiana leaves (1.67+1.528), vines (7.67±2.96) and tubers (12.67+2.309) was significantly less compared with other Ipomoea sp. Further, the two-choice bioassay was done, using I. batatas and I. mauritiana for comparison. Based on the morphological screening different phytochemical constituents was identified using GC-MS analysis of the methanolic extract of roots of selected Ipomoea sp. (I. mauritiana, I. palmata and I. batatas). The results indicated that the phytochemical constituent of I. mauritiana viz., undecane, quinic acid which is to have insecticidal activity. The major constituent of I. batatas comprises of melezitose (38.53%) and alpha-I-rhamnopyranose (21.26%). It can be concluded that the phytochemical constituents of I. mauritiana was responsible for the antibiosis.

Rapid and High Throughput Hydroponics Phenotyping Method for Evaluating Chickpea Resistance to Phytophthora Root Rot

Phytophthora root rot (PRR) is a major constraint to chickpea production in Australia. Management options for controlling the disease are limited to crop rotation and avoiding high risk paddocks for planting. Current Australian cultivars have partial PRR resistance, and new sources of resistance are needed to breed cultivars with improved resistance. Field- and glasshouse-based PRR resistance phenotyping methods are labour intensive, time consuming, and provide seasonally variable results; hence, these methods limit breeding programs’ abilities to screen large numbers of genotypes. In this study, we developed a new space saving (400 plants/m2), rapid (<12 days), and simplified hydroponics-based PRR phenotyping method, which eliminated seedling transplant requirements following germination and preparation of zoospore inoculum. The method also provided post-phenotyping propagation all the way through to seed production for selected high-resistance lines. A test of 11 diverse chickpea genotypes provided both qualitative (PRR symptoms) and quantitative (amount of pathogen DNA in roots) results demonstrating that the method successfully differentiated between genotypes with differing PRR resistance. Furthermore, PRR resistance hydroponic assessment results for 180 recombinant inbred lines (RILs) were correlated strongly with the field-based phenotyping, indicating the field phenotype relevance of this method. Finally, post-phenotyping high-resistance genotypes were selected. These were successfully transplanted and propagated all the way through to seed production; this demonstrated the utility of the rapid hydroponics method (RHM) for selection of individuals from segregating populations. The RHM will facilitate the rapid identification and propagation of new PRR resistance sources, especially in large breeding populations at early evaluation stages.

Identification of sources of resistance to scald (Rhynchosporium commune) and of related genomic regions using genome-wide association in a mapping panel of spring barley

Barley is an important crop worldwide known for its adaptation to harsh environments and used in multiple forms as feed, food and beverages. Its productivity is affected by major abiotic and biotic stresses. Scald caused by hemibiotrophic fungus Rhynchosporium commune is a major foliar disease in many parts of the world. Host plant resistance is targeted by breeders to efficiently control this disease. An association mapping panel of 316 spring barley genotypes (AM2017) was screened for seedling resistance in greenhouse against three R. commune isolates and for adult plant resistance in three field locations in Morocco. The phenotyping results showed different numbers of entries with resistant and moderately resistant reactions at both seedling and adult plant stages. The reactions differed between the isolates with the highest percentage of resistant genotypes observed for isolate SC-S611 (49.4%) and highest percentage of susceptible genotypes (73.8%) for isolate SC-1122. At adult plant stage, the highest percentage of scald resistant genotypes (64.5%) was observed at Rommani site compared to 56% at Guich site and only 28.8% at Marchouch site. Seven genotypes were resistant at the seedling and adult plant stages. Genome wide association study (GWAS) revealed 102 MTA (15 QTL) at the seedling stage, and 25 MTA (12 QTL) associated with scald resistance at the adult plant stage. In addition, the sequences of 92 out of 102 at SRT, and 24 out of 25 significant SNP markers at APR were located in genomic regions enriched with functional proteins involved in diverse cellular processes including disease resistance. These markers span over all chromosomes with the majority of SNPs located on 3H and 7H. This study has verified 18 QTL reported in previous studies. In addition, it was successful in identifying new sources of resistance and novel genomic regions which could help in enhancing scald resistance in barley breeding programs.

Phenotypic response of a core collection of Aegilops triuncialis accessions to wheat leaf rust and expression pattern of genes involved in resistance

AbstractLeaf rust caused by Puccinia triticina Eriks. is a serious threat to wheat production worldwide. Exploiting wild relatives can effectively help to improve the genetic resistance of wheat against rust. This study aimed to evaluate the responses of 34 Aegilops triuncialis accessions to seven Pt pathotypes and to analyse expression of genes associated with resistance at the seedling stage. Following multipathotype testing, two accessions with contrasting resistance were analysed at 0, 6, 12 and 24 h post‐inoculation for the expression profile of genes related to PR1, PR2, PR4, PR9, phenylalanine ammonia‐lyase and ATP‐binding cassette transporter. Of the accessions tested, eight showed high infection types of “3” to at least one Pt pathotype, while the remaining accessions had low ITs (“0;=” to “2+”) against all pathotypes. The relative expressions of all candidate genes increased at all‐time points, but the expression level in the incompatible interaction was significantly higher than that of the compatible. The close relationship between PR proteins, PAL, salicylic acid‐ and jasmonic acid‐responsive proteins, as well as the proteins involved in the production of reactive oxygen species and lignin, could point to the specific recognition of the pathogen followed by the timely and intense induction of the expression of PR genes as the main reasons for resistance in incompatible interaction. In conclusion, the present study identified potentially new sources of resistance in this Ae. triuncialis population, which can be exploited in wheat breeding programs.

Multi-Environment Testing Based G × E Interactions Reveal Stable Host-Plant Resistance against Sterility Mosaic Disease in Pigeonpea

Sterility mosaic disease (SMD) is a serious biotic restraint in pigeonpea-growing regions of the Indian subcontinent. Disease control using chemicals like acaricides is not economical or sustainable, pointing towards host plant resistance as the ideal strategy for its management. In this study, from preliminary screening of 75 pigeonpea germplasm accessions and breeding lines, 21 pigeonpea genotypes showing moderate resistance to SMD were selected and again assessed at two multi-environment locations during Kharif 2021/2022 and 2022/2023. Analysis of variance partitioned the variation between the main effects of genotype and genotype × environment (GGE). The results revealed a significant variation (p ˂ 0.05) in the SMD incidence between the tested genotypes, environment, and their interactions. Genotype variance contributed the greatest effect (63.56%) to the total variation and it represents the maximum disease variation. Furthermore, a significant positive correlation was found for the levels of SMD incidence between the test environments. We observed that SMD incidence had a high negative correlation with the maximum temperature (r = −0.933), and positively correlated with the rainfall (r = 0.502). Analysis of principal components 1 and 2 of the GGE explained 95.33% of the total variation and identified 10 genotypes (G1, G3, G4, G8, G10, G12, G13, G15, G20, and G21) showing moderate resistance stability across the environments. As new sources of resistance to SMD, these genotypes should be incorporated in pigeonpea breeding trials for further release. This research broadens the area of phenotyping and identifies stable resistance sources that can be used in future SMD resistance breeding projects.

Estimation of Genetic Parameters and Identification of Leaf Blast-Resistant Rice RILs Using Cluster Analysis and MGIDI

Rice blast disease, caused by the fungus Magnaporthe oryzae, poses a significant threat to rice cultivation. One effective way to deal with this disease is to identify and introduce resistant varieties using different breeding methods. This study utilized a population of 153 recombinant inbred lines (RILs) derived from the crossing of the Shahpasand (SH) and IR28 varieties, characterized by susceptibility and resistance to leaf blast, respectively. In combination with 12 control varieties, these genotypes were subjected to an extensive evaluation of disease severity (5 stages), the area under the disease progress curve (AUDPC), type, and the infection rate in 2021 and 2022. Analysis of variance revealed significant genetic variation, highlighting the potential of the RIL population for identifying and selecting resistant lines. Employing cluster analysis and the multi-trait genotype-ideotype distance index (MGIDI), 17 lines were identified as the most resistant over a two-year evaluation period. The average AUDPC for these resistant lines was estimated at 2.435 ± 0.114, and lines 17 and 111 had the lowest AUDPC (1.526 and 1.630, respectively) and showed the least infection in two years. Conversely, lines 42 and 43 showed the highest AUDPC values (255.312 and 248.209) along with heightened sensitivity. The use of MGIDI yielded a substantial selection differential (SD) of −59.12% for traits related to leaf blast disease resistance, demonstrating the effectiveness of this method. Furthermore, new recombinant populations are expected to be developed in future plant breeding projects by crossing the most susceptible and resistant lines, which will be new sources of resistance to this disease.

Identification of resistance to Sugarcane mosaic virus, Sugarcane streak mosaic virus, and Sugarcane bacilliform virus in new elite sugarcane accessions in India.

Sugarcane mosaic and leaf fleck diseases are significant viral diseases affecting sugarcane crops in India. The use of resistant sugarcane varieties is considered the most economical and effective approach to manage viral diseases, especially in vegetatively propagated crops such as sugarcane. Sugarcane mosaic virus (SCMV) and Sugarcane streak mosaic virus (SCSMV) are the primary pathogens responsible for mosaic disease in sugarcane-growing regions of India. Sugarcane bacilliform virus (SCBV), causing leaf fleck disease, is also often found in mixed infections with mosaic symptoms. The study aimed to identify new sources of resistance by screening sugarcane germplasm for resistance to SCMV, SCSMV, and SCBV. The screening was carried out under high inoculum using the infector row method in both plant and ratoon crops. Out of 129 genotypes tested, only 8 were found to be free of mosaic viruses, indicating a rare occurrence of resistant sources. The study revealed that mosaic disease is widespread, with nearly 95% of tested varieties/genotypes being infected with mosaic viruses. SCMV, SCSMV, and SCBV were detected in 121 out of 129 genotypes using the RT-PCR and PCR assays. Based on their response to the viruses, the tested genotypes were categorized into different resistance grades: highly resistant (grade 1), resistant (grade 2), moderately resistant (grade 3), susceptible (grade 4), and highly susceptible (grade 5). The results of the study provide valuable information about elite resistance resources that can be used for the prevention and control of mosaic disease. These resistant genotypes could also serve as potential donors for mosaic and leaf fleck disease resistance in breeding programs.