Search Results (107)

Clubroot disease caused by Plasmodiophora brassicae has greatly affected the quality and yield of Chinese cabbage. Excavating the key resistance genes and verifying their function is important for clarifying disease resistance mechanisms. Virus-induced gene silencing (VIGS) technology has been widely used in gene function research. However, the VIGS system specifically designed for the functional analysis of clubroot resistance genes is currently unavailable. In this study, it was found that the vacuum infiltration VIGS method is more effective for gene silencing than the seed soaking method. When seedlings were VIGS-treated using vacuum infiltration for 10 min, genes were effectively silenced on the 6th-35th days (d) after treatment, ensuring high seedling survival rate and plant transformation rate. To investigate the optimal inoculation time with P. brassicae, plants were inoculated 3, 6, 9, and 15 d after VIGS treatment. Results showed that the difference of clubroot resistance between gene-silenced and control plants was most significant when plants were inoculated 6 d after VIGS treatment. This result suggests that, when the target gene began to silence (6 d after VIGS), immediate inoculation with P. brassicae should be suitable for the functional study of clubroot-resistance genes. Full article

Breeding for disease-resistant varieties is a sustainable solution to reduce substantial production losses caused by pathogenic infestations in Brassica vegetables, bypassing environmentally risky disease management practices. Host-resistant genetic mechanisms aid breeders to identify resistance loci and linked markers for the clubroot, Fusarium yellows, downy mildew, black rot, stem rot, soft rot, white rust, and turnip mosaic virus diseases in Brassica vegetables. Introgression of the resistance (R) genes by marker-assisted selection (MAS) breeding strategies allow the development of disease-resilient varieties. Brassica rapa clubroot-resistant genes (CRa, CRc, CRd, CRk, and Crr5) have been introgressed into Chinese cabbage, while CR genes (CRa, CRb, CRc, Crr1, Crr2, and Crr3) from B. rapa were also introgressed into B. oleracea. Beyond MAS, R genes can be precisely engineered by CRISPR-based technologies into precise and durable resistant varieties. The involvement of DNA methylation and histone modifications epigenetically regulate resistance mechanisms, often via ethylene/salicylic acid/jasmonic acid signaling pathways. DNA methylation mediates systemic acquired resistance by the differential expression of genes such as JAZ1, PR3, and NDR1. Future progress will depend on identifying epiQTLs and epi-markers linked to R genes. Epigenetic insights with genetic knowledge will facilitate breeding of biotic stress-resilient Brassica vegetables. This review synthesizes current molecular understanding of biotic stressors and provides future directions for disease resistance breeding of Brassica vegetable plants. Full article

Clubroot disease, caused by Plasmodiophora brassicae, is a major global threat, causing severe yield losses of up to 100% in heavily infested fields. Interspecific hybridization is essential for the transfer of clubroot resistance genes among the Brassica species. This review aimed to describe the sources of clubroot resistance, categorize their types in Brassica crops, and identify the most effective techniques and underutilized sources for both intergeneric and interspecific hybridization. A systematic literature review served as the foundation for expert analysis, encompassing a comprehensive list of known sources of resistance and a detailed description of their characteristics, including monogenic, polygenic, dominant, and recessive traits. In addition, this review specifies techniques suitable for gene transfer, such as markers, embryo rescue, somatic hybridization, and CRISPR/Cas. Based on the literature, underutilized directions for genetic crosses have been proposed. These conclusions suggest that combining biotechnological methods, including markers, CRISPR/Cas, and embryo rescue, with intergeneric crosses offers the potential to transfer resistance genes from previously untapped sources. Full article

Modern head cabbage (Brassica oleracea var. capitata L.) breeding is based on the application of molecular markers through marker-assisted selection (MAS). In hybrid breeding, critical markers are deployed to assess cytoplasmic male sterility (CAPS and SSR for orf138), genic male sterility (KASP markers for Ms-cd1, InDel for ms3, and BoCYP704B1), fertility restoration (InDel marker for Rfo), combining ability and genetic diversity (using SSR and KASP marker sets), and to ensure F₁ hybrid seed genetic purity (RAPD and SSR markers sets). Disease resistance, a well-developed category due to frequent monogenic control, includes markers for major pathogens, including those for Fusarium wilt (for Foc-Bo1 gene), black rot (race 1–7 specific SSR and InDel markers), clubroot (Kamogawa, Anno, and Yuki isolates), and downy mildew (BoDMR2 InDel marker). Markers have also been identified for key agronomic and morphological traits, such as those governing petal color (InDel markers for BoCCD4), leaf waxiness (BoGL1, BoGL-3, Cgl1, Cgl2, BoWax1, and BoCER2), and leaf color (ygl-1, BoMYB2, BoMYBL2-1). The review also included markers for resistance to abbioticaly induced negative physiological processes, such as head splitting (QTL SPL-2-1, Bol016058), bolting (resistance loci-associated SSR marker), prolonged flowering time (BoFLC1,2 genes), and high- and low-temperature tolerance (BoTPPI-2, BoCSDP5, BoCCA1). Despite these advancements, the review highlights that the marker repertoire for cabbage remains limited compared with other Brassicaceae species, particularly for complex polygenic traits. This synthesis is a valuable resource for breeders and researchers, facilitating the development of superior head cabbage cultivars and hybrids. Full article

Clubroot, caused by Plasmodiophora brassicae, is a destructive disease of Chinese cabbage (Brassica rapa ssp. pekinensis) at all growing stages. Early detection of the disease is essential to mitigate the impact of clubroot. Here, we established an optimal algorithm for multispectral imaging combined with machine learning to detect leaf responses of highly susceptible cultivar YoulvNo.3 at different day after inoculation (DAI). Spectral data at 19 wavelengths were collected from leaf multispectral images, and key characteristic wavelengths were further extracted. Principal Component Analysis (PCA) revealed a clear separation between healthy and infected samples at 11 DAI. Four classification algorithms, including Random Forest (RF), Partial Least Squares Discriminant Analysis (PLS-DA), Support Vector Machine (SVM) and Extreme Learning Machine (ELM), were employed to construct early detection model for clubroot. SVM achieved over 81% accuracy with full-spectrum data, while ELM based on characteristic wavelengths provided the best performance, accuracy exceeding 84%. Stratified five-fold cross-validation was used to validate the optimal model. An average accuracy of 83.79% (±1.04%) and macro-averaged F1-score of 82.13% (±1.12%) across validation folds were obtained, confirming stable performance. Our findings, for the first time, identified detectable spectral differences between the healthy and infected plants at 11 DAI using leaf multispectral combined with machine learning, providing a potential application for early detection of clubroot and timely control in Chinese cabbage. Full article

Clubroot in cruciferous plants remains a significant threat to growers worldwide. We investigated whether humic acid material (HAM) could control clubroot in Chinese cabbage and broccoli as an alternative to fungicides. Six independent experiments were conducted, and the results were analyzed using a general liner mixed model (GLMM) and a network meta-analysis (NMA). Some HAM treatments significantly controlled clubroot incidence on Chinese cabbage in three experiments, but no significant effects were observed in the others. HAM treatment effects varied across experiments. The GLMM indicated that HAM treatment and the interaction between the HAM amount and planting timing were significantly associated with disease incidence. HAM effectiveness depended on application amount and planting timing after treatment. The NMA estimated a statistically significant risk ratio of 0.85 for planting four weeks after HAM treatment, suggesting low efficacy in suppressing clubroot. Two field trials aligned with the greenhouse results. Full article

Clubroot disease, caused by Plasmodiophora brassicae, is a threat to Brassica crops; therefore, understanding of host-resistance is important for developing clubroot-resistant cultivars. Using multi-omics analysis of clubroot-resistant (CR) and -susceptible (CS) near-isogenic lines (NILs) of B. napus, carrying the resistance of turnip (B. rapa var. rapifera), we characterized the host resistance mechanisms. Through proteome analysis, we identified 6626 differentially abundant proteins (DAPs) (2353 in CR-NILs, 4273 in CS-NILs) (q < 0.05), of which 50 in CR- and 62 in CS-NILs were detected across the disease developmental stages. Notable proteins included those involved in reactive oxygen species scavenging (BnaA09T0647200WE)], cell-wall modifications (BnaA04T0244300WE) and glucosinolate biosynthesis (BnaA01T0266700WE) in the CR-NILs. Additionally, disease-resistance proteins like ENHANCED DISEASE RESISTANCE 2-like (BnaA03T0055600WE) and hairpin-induced family protein YLS9 (BnaA08T0237900WE) showed increased abundance in CR-NILs. In contrast, CS-NILs exhibited decreased abundance of defense-related proteins, including proteins containing CUPIN domain (BnaA09T0578800WE) and LACCASE (BnaA02T0019200WE). Integration of proteome data with transcriptome data revealed 33 genes in CR- and 32 in CS-NILs showing a consistent pattern, including the genes related to PLANT INVERTASE/PECTIN METHYLESTERASE INHIBITOR (BnaC04T0003100WE), KELCH MOTIF (BnaC02T0374800WE), LACCASE (BnaA02T0019200WE), and antioxidant-related transcripts [GLUTATHIONE S-TRANSFERASES (BnaA03T0280900WE) and 4-HYDROXYPHENYLPYRUVATE DIOXYGENASE (BnaA09T0641500WE)]. Our findings offer valuable new targets for breeding clubroot-resistant B. napus. Full article

Clubroot, caused by the obligate parasite Plasmodiophora brassicae, is a soilborne disease affecting canola (Brassica napus) and other crucifers. Although planting resistant cultivars remains the primary strategy for managing clubroot, the emergence of resistance-breaking P. brassicae pathotypes continues to threaten canola production. In this context, soil and root microorganisms may play a role in suppressing the disease. This study investigated the impact of P. brassicae infection on the microbial communities of soil, seeds, roots, and the rhizosphere in susceptible and resistant canola lines, with the aim of analyzing host–pathogen–microbiome interactions and identifying microbial taxa potentially associated with disease resistance. Our findings showed that resistant canola lines inoculated with P. brassicae (pathotype 3A) exhibited reduced disease severity compared to their susceptible counterparts. Diversity analyses of microbial communities revealed that clubroot-resistant canola lines tended to maintain more stable and diverse fungal communities, with a higher Shannon index than susceptible lines. Inoculation with P. brassicae induced more pronounced changes in the root microbiome than in the rhizosphere. Additionally, the seed microbiomes of resistant and susceptible lines displayed distinct bacterial and fungal profiles, suggesting that clubroot susceptibility may influence seed-associated microbial community composition. Differential abundance analysis of root and rhizosphere microbiomes indicated that certain microbial taxa, including bacterial genera such as Acidovorax, Bacillus, Cupriavidus, Cytophaga, Duganella, Flavobacterium, Fluviicola, Luteimonas, Methylotenera, Pedobacter, and Peredibacter, as well as fungal genera such as Aspergillus, Candida, Fusicolla, Paecilomyces, and Rhizophlyctis, may be recruited or enriched in resistant canola lines following P. brassicae inoculation, potentially contributing to reduced clubroot severity. Full article

Clubroot disease, caused by Plasmodiophora brassicae, poses a serious threat to global Brassica crop production. Orphan genes (OGs), which are species or lineage-specific and lack detectable homologs in other taxa, have been implicated in various biotic stress responses. Here, we identified a novel Brassica rapa-specific orphan gene, designated CROG1, that confers resistance to clubroot. Heterologous overexpression of CROG1 in Arabidopsis thaliana significantly enhanced resistance to P. brassicae. Transcriptomic profiling of CROG1-overexpressing lines highlighted the essential role of the phenylpropanoid biosynthesis pathway, showing upregulation of key lignin synthesis genes (including CCoAMT, CAD6, PER4, and AZI1) and defense-related regulators (RBOHC and WAKs). Weighted co-expression network analysis further corroborated the link between CROG1-mediated resistance and enhanced lignin deposition and cell wall reinforcement. Our findings establish CROG1 as a Brassica-specific orphan gene that enhances clubroot resistance via phenylpropanoid pathway activation. These results highlight the potential of orphan genes as novel genetic resources for breeding clubroot-resistant Brassica varieties, offering a sustainable strategy to mitigate yield losses caused by this devastating disease. Full article

Clubroot, caused by Plasmodiophora brassicae Woronin, poses a major threat to Chinese cabbage (Brassica rapa subsp. pekinensis) production worldwide, significantly impacting crop yield, quality, and economic value. Biological control represents a promising approach since it is non-toxic and eco-friendly, and it reduces the risk of pathogen resistance development. In this study, our objective was to screen for actinomycetes that can effectively inhibit clubroot. We screened 13 actinomycete strains, identifying 2, XDS3-6 and CD1-1, with substantial in vivo inhibitory effects, achieving infection suppression rates above 64% against P. brassicae. Phylogenetic analysis classified XDS3-6 and CD1-1 as Streptomyces virginiae and Streptomyces cinnamonensis, respectively. Both strains exhibited protease and glucanase production capabilities, essential for pathogenic suppression. Additionally, these strains induced host defense responses, as evidenced by increased jasmonic acid (JA) and salicylic acid (SA) accumulation and elevated activities of defense-related enzymes. Colonization studies of XDS3-6 and CD1-1 mutant strains in cabbage roots indicated sustained root colonization, with peak colony-forming units (CFUs) at 20 days post-inoculation, reaching 11.0 × 10⁴ CFU/g and 8.5 × 10⁴ CFU/g, respectively, and persisting for at least 30 days. Overall, these findings underscore the potential of Streptomyces strains XDS3-6 and CD1-1 as effective biocontrol agents, providing a theoretical foundation for their application in managing clubroot in Chinese cabbage. Full article

Clubroot is a destructive soilborne disease caused by Plasmodiophora brassicae that threatens the production of Chinese cabbage. The molecular mechanisms underlying the resistance of Chinese cabbage to clubroot remains unclear, making the identification and analysis of resistance genes crucial for developing resistant varieties. Comparative transcriptome analysis of roots from the resistant line “JJ S5-1” and the susceptible line “SYY10-1” revealed significant differences in gene expression profiles at various stages after inoculation. Weighted gene coexpression network analysis revealed midnight blue and green modules as substantially associated with disease response, with each showing positive regulatory patterns. Several defense-related genes and transcription factors important for resistance to Plasmodiophora brassicae were identified, including disease resistance proteins, PR1, PBS1, and TGA, and WRKY transcription factors, most of which were upregulated following inoculation. Key genes associated with trait-related expression patterns were analyzed and a working model was proposed to explain the mechanism of clubroot disease resistance to Plasmodiophora brassicae infection in Chinese cabbage. These findings offer a valuable resource for further investigation of the immune response in the resistance of “JJ S5-1” to clubroot disease. Full article

Clubroot disease, caused by the soil-borne pathogen Plasmodiophora brassicae, poses a severe threat to the global production of Brassicaceae crops, including radish (Raphanus sativus L.). Although resistance breeding is an important method for sustainable disease management, the molecular mechanism underlying clubroot resistance remains elusive in radish compared to other Brassicaceae species. In this study, 52 radish inbred lines were screened for disease responses following P. brassicae inoculation, with the resistant line T6 and the susceptible line T14 selected for transcriptome analysis. RNA-Seq was performed at 10, 20, and 30 days post inoculation (DPI) to elucidate transcriptional responses. The susceptible line T14 exhibited a higher number of differentially expressed genes (DEGs) and persistent upregulation across all time points, indicating ineffective defense responses and metabolic hijacking by the pathogen. In contrast, the resistant line T6 displayed temporally coordinated defense activation marked by rapid induction of core immune mechanisms: enhanced plant–pathogen interaction recognition, MAPK cascade signaling, and phytohormone transduction pathways, consistent with effector-triggered immunity priming and multilayered defense orchestration. These findings indicate that resistance in T6 could be mediated by the rapid activation of multilayered defense mechanisms, including R gene-mediated recognition, MAPK-Ca²⁺-ROS signaling, and jasmonic acid (JA) pathway modulation. The outcomes of this study would not only facilitate clarifying the molecular mechanism underlying clubroot resistance, but also provide valuable resources for genetic improvement of clubroot resistance in radish. Full article

The proline-rich extensin-like receptor kinase (PERK) gene family is crucial to various molecular and cellular processes in plants. We identified 50 PERK genes in Brassica napus to explore their evolutionary dynamics, structural diversity, and functional roles. These genes were grouped into four classes and unevenly distributed across 18 chromosomes. Phylogenetic studies and Ka/Ks ratios revealed purifying selection during the evolution process. They exhibited significant diversification in gene length, molecular weight, and isoelectric points, suggesting specialized function. Gene structure and motif analyses revealed variations among the BnPERK family members, with conserved tyrosine kinase domains suggesting functional importance. Cis-element analysis predicted the involvement in hormone signaling and stress responses. Expression profiling showed diverse patterns across tissues and hormone treatments, highlighting potential roles in growth regulation and hormone signaling. Protein–protein interaction networks suggested BnPERK proteins interact with a wide array of proteins, implicating them in multiple biological processes. The transcriptional downregulation of four BnPERK genes upon Plasmodiophora brassicae infection implied a role in clubroot disease response. Furthermore, the Arabidopsis perk9 mutant displayed relieved disease severity and enhanced basal immune response, suggesting the negative role of PERK9 in plant immunity. The study highlighted the potential role of BnPERKs in crop improvement strategies against clubroot disease. Full article

Elemental sulfur, commonly known for its wide range of biological activities, has a long history of use in protecting all garden and vegetable crops from a range of pests and diseases, including powdery mildew, ascochyta blight, clubroot, plant mites, oidium, anthracnose, and scab. In the present study, a quick and environmentally friendly approach has been developed for the synthesis of sulfur nanoparticles with antibacterial activity. Fine sulfur particles (FSPs) were prepared by modifying the surface of elemental sulfur using various polyelectrolyte–surfactant mixtures (PSMs) including sodium carboxymethyl cellulose–sodium dodecylbenzene sulfonate (NaCMC-SDBS) and polyhexamethylene guanidine hydrochloride–cetyltrimethylammonium bromide (PHMG-CTAB). The FSPs were characterized by UV–visible spectrophotometry, X-ray diffraction (XRD), thermogravimetric/differential scanning calorimetry analysis (TG/DSC), and scanning electron microscopy (SEM), with the FSPs showing an almost spherical shape with an average size in the range of 150–200 nm. The antibacterial activity of the FSPs was tested against Gram-positive Staphylococcus aureus and Enterococcus faecium and Gram-negative Escherichia coli and Pseudomonas aeruginosa bacteria and one fungus (Aspergillus brasiliensis ATCC 95 16404). Based on this, it could be seen that FSPs exhibited significant antimicrobial activity against Gram-positive bacteria, i.e., S. aureus and E. faecium. The in vitro cytotoxicity of the FSPs-1 and FSPs-2 studied in normal (MeT-5A) and tumorous (MCF-7) human cell lines was assessed in the concentration range from 500 μg/mL to 0.12 mg/mL, from which it was determined as being non-cytotoxic. The received products can be considered for potential application in agriculture and medicine. Full article

The effect of crop rotation on soil-borne diseases is a representative case of plant–soil feedback in the sense that plant disease resistance is influenced by soils with different cultivation histories. This study examined the microbial mechanisms inducing the differences in the clubroot (caused by Plasmodiophora brassicae pathogen) damage of Chinese cabbage (Brassica rapa subsp. pekinensis) after the cultivation of different preceding crops. It addresses two key questions in crop rotation: changes in the soil bacterial community induced by the cultivation of different plants and the microbial mechanisms responsible for the disease-suppressive capacity of Chinese cabbage. Twenty preceding crops from different plant families showed significant differences in the disease damage, pathogen density, and bacterial community composition of the host plant. Structural equation modelling revealed that the relative abundance of four key bacterial orders in Chinese cabbage roots can explain 85% and 70% of the total variation in pathogen density and disease damage, respectively. Notably, the relative dominance of Bacillales and Rhizobiales, which have a trade-off relationship, exhibited predominant effects on pathogen density and disease damage. The disease-suppressive soil legacy effects of preceding crops are reflected in compositional changes in key bacterial orders, which are intensified by the bacterial community network. Full article