Resistance Of Cabbage Research Articles

Identification and expression profiling analysis of NBS-LRR genes involved in Fusarium oxysporum f.sp. conglutinans resistance in cabbage.

As one of the most important resistance (R) gene families in plants, the NBS-LRR genes, encoding proteins with nucleotide-binding site (NBS) and leucine-rich repeat (LRR) domains, play significant roles in resisting pathogens. The published genomic data for cabbage (Brassica oleracea L.) provide valuable data to identify and characterize the genomic organization of cabbage NBS-LRR genes. Ultimately, we identified 105 TIR (N-terminal Toll/interleukin-1 receptor)-NBS-LRR (TNL) genes and 33 CC (coiled-coil)-NBS-LRR (CNL) genes. Further research indicated that 50.7% of the 138 NBS-LRR genes exist in 27 clusters and there are large differences among the gene structures and protein characteristics. Conserved motif and phylogenetic analysis showed that the structures of TNLs and CNLs were similar, with some differences. These NBS-LRRs are evolved under negative selection and mostly arose from whole-genome duplication events during evolution. Tissue-expression profiling of NBS-LRR genes revealed that 37.1% of the TNL genes are highly or specifically expressed in roots, especially the genes on chromosome 7 (76.5%). Digital gene expression and reverse transcription PCR analyses revealed the expression patterns of the NBS-LRR genes upon challenge by Fusarium oxysporum f.sp. conglutinans: nine genes were upregulated, and five were downregulated. The major resistance gene Foc1 probably works together with the other four genes in the same cluster to resist F. oxysporum infection.

Genome-wide characterization and expression profiling of SWEET genes in cabbage (Brassica oleracea var. capitata L.) reveal their roles in chilling and clubroot disease responses

BackgroundThe SWEET proteins are a group of sugar transporters that play a role in sugar efflux during a range of biological processes, including stress responses. However, there has been no comprehensive analysis of the SWEET family genes in Brassica oleracea (BoSWEET), and the evolutionary pattern, phylogenetic relationship, gene characteristics of BoSWEET genes and their expression patterns under biotic and abiotic stresses remain largely unexplored.ResultsA total of 30 BoSWEET genes were identified and divided into four clades in B. oleracea. Phylogenetic analysis of the BoSWEET proteins indicated that clade II formed first, followed by clade I, clade IV and clade III, successively. Clade III, the newest clade, shows signs of rapid expansion. The Ks values of the orthologous SWEET gene pairs between B. oleracea and Arabidopsis thaliana ranged from 0.30 to 0.45, which estimated that B. oleracea diverged from A. thaliana approximately 10 to 15 million years ago. Prediction of transmembrane regions showed that eight BoSWEET proteins contain one characteristic MtN3_slv domain, twenty-one contain two, and one has four. Quantitative reverse transcription-PCR (qRT-PCR) analysis revealed that five BoSWEET genes from clades III and IV exhibited reduced expression levels under chilling stress. Additionally, the expression levels of six BoSWEET genes were up-regulated in roots of a clubroot-susceptible cabbage cultivar (CS-JF1) at 7 days after inoculation with Plasmodiophora brassicae compared with uninoculated plants, indicating that these genes may play important roles in transporting sugars into sink roots associated with P. brassicae colonization in CS-JF1. Subcellular localization analysis of a subset of BoSWEET proteins indicated that they are localized in the plasma membrane.ConclusionsThis study provides important insights into the evolution of the SWEET gene family in B. oleracea and other species, and represents the first study to characterize phylogenetic relationship, gene structures and expression patterns of the BoSWEET genes. These findings provide new insights into the complex transcriptional regulation of BoSWEET genes, as well as potential candidate BoSWEET genes that promote sugar transport to enhance chilling tolerance and clubroot disease resistance in cabbage.

Comparative transcriptomic analysis reveals gene expression changes during early stages of Plasmodiophora brassicae infection in cabbage (Brassica oleracea var. capitata L.)

Clubroot caused by Plasmodiophora brassicae is an economically important disease of crucifer crops throughout the world and is a major threat to the quality and yield of cabbage (Brassica oleracea var. capitata L.) in China. Host resistance is essential for clubroot management. Although two cabbage lines (clubroot-resistant line CR21 and clubroot-susceptible line CS54) have been identified through screening 80 cabbage accessions, the molecular mechanisms underlying differential responses to clubroot remain elusive. Herein, RNA-seq analysis was performed to characterize the transcriptomic changes in CR21 and CS54 at 3 days after P. brassicae inoculation (DAI). In total, 1057 and 4741 differentially expressed genes (DEGs) were found in CR21 and CS54, respectively. Moreover, 541 genes were up-regulated in CR21, but showed either no significant change or were down-regulated in CS54. Gene Ontology (GO) analysis showed that most DEGs were involved in metabolism, transport, signal transduction and defence. Compared with the identified putative defence response genes in Arabidopsis thaliana, 165 resistance-related DEGs were obtained, including PAMPs-triggered immunity (PTI)-related genes and Effector-triggered-immunity (ETI)-related genes. Interestingly, the co-supported defence response DEGs contained the defence-related genes, wound response genes, RBOHB, WRKY28, TIR-NBS-LRR class (RPS4 etc.), pathogenesis-related (PR) gene (Bo7g005050), lipid transfer protein class (LTP1 etc.), plant hormone-related genes, ethylene signalling transduction (HRE1-like gene and EIN3), ABA signalling (PP2C and PYL13), and cell wall modification related genes (EXP17 and PME44, beta-1,3-glucanase and cytochrome P450 genes). Taken together, this study provided a comprehensive insight into transcriptomic responses to P. brassicae infection in two different cabbage lines, and identified several candidate genes that might contribute to clubroot resistance in cabbage and other Brassica crops.

Glucosinolate Profiling and Expression Analysis of Glucosinolate Biosynthesis Genes Differentiate White Mold Resistant and Susceptible Cabbage Lines.

Sclerotinia stem rot (white mold), caused by the fungus Sclerotinia sclerotiorum, is a serious disease of Brassica crops worldwide. Despite considerable progress in investigating plant defense mechanisms against this pathogen, which have revealed the involvement of glucosinolates, the host–pathogen interaction between cabbage (Brassica oleracea) and S. sclerotiorum has not been fully explored. Here, we investigated glucosinolate profiles and the expression of glucosinolate biosynthesis genes in white-mold-resistant (R) and -susceptible (S) lines of cabbage after infection with S. sclerotiorum. The simultaneous rise in the levels of the aliphatic glucosinate glucoiberverin (GIV) and the indolic glucosinate glucobrassicin (GBS) was linked to white mold resistance in cabbage. Principal component analysis showed close association between fungal treatment and cabbage GIV and GBS contents. The correlation analysis showed significant positive associations between GIV content and expression of the glucosinolate biosynthesis genes ST5b-Bol026202 and ST5c-Bol030757, and between GBS content and the expression of the glucosinolate biosynthesis genes ST5a-Bol026200 and ST5a-Bol039395. Our results revealed that S. sclerotiorum infection of cabbage induces the expression of glucosinolate biosynthesis genes, altering the content of individual glucosinolates. This relationship between the expression of glucosinolate biosynthesis genes and accumulation of the corresponding glucosinolates and resistance to white mold extends the molecular understanding of glucosinolate-negotiated defense against S. sclerotiorum in cabbage.

Combining QTL mapping with transcriptome and metabolome profiling reveals a possible role for ABA signaling in resistance against the cabbage whitefly in cabbage.

Whiteflies are among the world’s most significant agricultural pests and chemical insecticides are extensively used to reduce crop damage to acceptable levels. However, nearly all insecticides pose a threat to the environment and alternative control methods, such as breeding of crop varieties that are inherently insect-resistant, are needed. Previously, a strong source of plant-age dependent resistance to the cabbage whitefly (Aleyrodes proletella) has been identified in the modern white cabbage (Brassica oleracea var. capitata) variety Rivera. However, nothing is known about the molecular mechanisms or the genes involved in this resistance. In the present study, a multidisciplinary approach combining transcriptome and metabolome profiling with genetic mapping was used to identify the molecular players of whitefly resistance in cabbage. Transcriptome profiles of young (susceptible) and older (resistant) Rivera plants were analyzed using RNA sequencing. While many genes involved in general processes were differentially expressed between both ages, several defense-related processes were overrepresented in the transcriptome profile of older plants. Hormone measurements revealed that jasmonic acid (JA) levels decreased upon whitefly infestation at both plant ages. Interestingly, abscisic acid (ABA) levels showed contrasting effects in response to whitefly infestation: ABA levels were reduced in young plants but induced in older plants upon whitefly feeding. Auxin levels were significantly lower in older plants compared with young plants, independent of whitefly presence, while glucosinolate levels were higher. Additionally, whitefly performance was monitored in an F2 population derived from a cross between Rivera and the susceptible white cabbage variety Christmas Drumhead. Significant QTL intervals were mapped on chromosome 2 and 9 for oviposition rate and whitefly adult survival, respectively. Several genes that were higher expressed in older plants and located in the identified QTL intervals were orthologous to Arabidopsis genes that have been related to ABA signaling, suggesting a role for ABA in the regulation of resistance towards whiteflies. Our results show that combining different omics approaches is a useful strategy to identify candidate genes underlying insect resistance.

Altered Glucosinolate Profiles and Expression of Glucosinolate Biosynthesis Genes in Ringspot-Resistant and Susceptible Cabbage Lines.

Ringspot, caused by the fungus Mycosphaerella brassicicola, is a serious disease of Brassica crops worldwide. Despite noteworthy progress to reveal the role of glucosinolates in pathogen defense, the host–pathogen interaction between cabbage (Brassica oleracea) and M. brassicicola has not been fully explored. Here, we investigated the glucosinolate profiles and expression of glucosinolate biosynthesis genes in the ringspot-resistant (R) and susceptible (S) lines of cabbage after infection with M. brassicicola. The concomitant rise of aliphatic glucoiberverin (GIV) and indolic glucobrassicin (GBS) and methoxyglucobrassicin (MGBS) was linked with ringspot resistance in cabbage. Pearson’s correlation and principle component analysis showed a significant positive association between GIV contents and the expression of the glucosinolate biosynthesis gene ST5b-Bol026202 and between GBS contents and the expression of the glucosinolate biosynthesis gene MYB34-Bol017062. Our results confirmed that M. brassicicola infection induces the expression of glucosinolate biosynthesis genes in cabbage, which alters the content of individual glucosinolates. This link between the expression of glucosinolate biosynthesis genes and the accumulation of their respective glucosinolates with the resistance to ringspot extends our molecular sense of glucosinolate-negotiated defense against M. brassicicola in cabbage.

Optimization of nanofibrillation degree of chitin for induction of plant disease resistance: Elicitor activity and systemic resistance induced by chitin nanofiber in cabbage and strawberry

Chitin has not been extensively used in agriculture owing to its handling difficulties despite its utilizable functions such as induction of disease resistance and growth promotion in plants. Chitin nanofiber (CNF), which has an elicitor activity to induce plant disease resistance, can be handled like a water-soluble material, because of its high dispersibility. To determine the potential use of CNF in agriculture, the nanofibrillation degree of chitin for elicitor activity and its effect on the disease resistance against pathogens were examined in cabbage and strawberry plants. The similarity in thickness and length of CNF to that of polymeric chitin was sufficient to induce elicitor activity in both plants. Cabbage and strawberry plants, which were grown in a mixture of soil and CNF with optimized specification, challenged with fungal pathogens showed a reduction in the number of spots caused by Alternaria brassicicola and lesion size by Colletotrichum fructicola, respectively. Gene expression analysis revealed that the defense-related genes in cabbage plant grown in CNF-containing soil were significantly upregulated before and after pathogen infection. These results indicate that CNF can systemically induce disease resistance in cabbage and strawberry plants and is a promising natural-based material to control diseases in cultivated plants.

Assessment of DNA markers for seed contamination testing and selection of disease resistance in cabbage

Cabbage (Brassica oleracea L. var. capitata) is an important vegetable worldwide. Most Japanese commercial cultivars of cabbage use an F1 hybrid seed production system. The purity of F1 hybrid seeds is important and the assessment of purity based on DNA markers can be highly accurate. In addition, selection of agronomically important traits such as disease resistance based on DNA markers is useful for breeding of cabbage. The aim of this study is to demonstrate the effectiveness of DNA marker-assisted selection in cabbage. In this study we distinguished the parental S haplotypes in 35 F1 hybrid cultivars by combining several linked DNA markers. Thirty-one highly polymorphic simple sequence repeats (SSR) markers were screened from 175 reported SSR markers, which are useful for assessment of the purity of F1 hybrid seeds. We examined the relationship between the DNA marker based genotype and the phenotype by an inoculation test of clubroot disease. A co-dominant PCR–RFLP marker was developed for selection of Fusarium yellows resistance and the genotypes using this marker were consistent with inoculation test in all tested samples.

Chrysophanol is involved in the biofertilization and biocontrol activities of Trichoderma

The effect of chrysophanol, a secondary metabolite of Trichoderma harzianum, on the growth and disease resistance of cabbage against Botrytis cinerea was investigated. Chrysophanol assisted cabbage growth and promoted resistance against B. cinerea. Proteins related to photosynthesis were expressed in T. harzianum- and chrysophanol-treated cabbages. The transcription levels of photosynthesis- and sucrose transport-related genes increased in chrysophanol-treated cabbages. The transcription levels of chitinase increased in T. harzianum-treated cabbages and those of ascorbate peroxidase in T. harzianum- and chrysophanol-treated cabbages. Chrysophanol is involved in stimulating plant growth and photosynthesis and in eliciting host defense responses during the colonization of T. harzianum.

Transcriptome Profiling of Resistance to Fusarium oxysporum f. sp. conglutinans in Cabbage (Brassica oleracea) Roots.

Fusarium wilt caused by Fusarium oxysporum f. sp. conglutinans (FOC) is a destructive disease of Brassica crops, which results in severe yield losses. There is little information available about the mechanism of disease resistance. To obtain an overview of the transcriptome profiles in roots of R4P1, a Brassica oleracea variety that is highly resistant to fusarium wilt, we compared the transcriptomes of samples inoculated with FOC and samples inoculated with distilled water. RNA-seq analysis generated more than 136 million 100-bp clean reads, which were assembled into 62,506 unigenes (mean size = 741 bp). Among them, 49,959 (79.92%) genes were identified based on sequence similarity searches, including SwissProt (29,050, 46.47%), Gene Ontology (GO) (33,767, 54.02%), Clusters of Orthologous Groups (KOG) (14,721, 23.55%) and Kyoto Encyclopedia of Genes and Genomes Pathway database (KEGG) (12,974, 20.76%) searches; digital gene expression analysis revealed 885 differentially expressed genes (DEGs) between infected and control samples at 4, 12, 24 and 48 hours after inoculation. The DEGs were assigned to 31 KEGG pathways. Early defense systems, including the MAPK signaling pathway, calcium signaling and salicylic acid-mediated hypersensitive response (SA-mediated HR) were activated after pathogen infection. SA-dependent systemic acquired resistance (SAR), ethylene (ET)- and jasmonic (JA)-mediated pathways and the lignin biosynthesis pathway play important roles in plant resistance. We also analyzed the expression of defense-related genes, such as genes encoding pathogenesis-related (PR) proteins, UDP-glycosyltransferase (UDPG), pleiotropic drug resistance, ATP-binding cassette transporters (PDR-ABC transporters), myrosinase, transcription factors and kinases, which were differentially expressed. The results of this study may contribute to efforts to identify and clone candidate genes associated with disease resistance and to uncover the molecular mechanism underlying FOC resistance in cabbage.

Identification of genes associated with black rot resistance in cabbage through suppression subtractive hybridization.

The suppression subtractive hybridization was employed to elucidate the resistance mechanism in Brassica oleracea var. capitata upon infection with Xanthomonas campestris pv. campestris. A cDNA library was constructed enriched in differentially expressed transcripts in the resistant cultivar Pusa mukta. A total of 150 unigenes were classified into five functional categories. The present study indicates that the defense-related unigenes accounted for the 35 % of the total unigenes studied. Confirmation of defense-specific representation genes through semiquantitative RT-PCR revealed their increased expression in the resistant cultivar which was validated by qPCR. The resistant cultivar elicited a strong hypersensitive response upon attack by black rot pathogen. The study is first of its kind where the resistant cultivar Pusa mukta in India has been assessed for its resistance to the bacterial pathogen.

Genome-wide SNP identification and QTL mapping for black rot resistance in cabbage.

BackgroundBlack rot is a destructive bacterial disease causing large yield and quality losses in Brassica oleracea. To detect quantitative trait loci (QTL) for black rot resistance, we performed whole-genome resequencing of two cabbage parental lines and genome-wide SNP identification using the recently published B. oleracea genome sequences as reference.ResultsApproximately 11.5 Gb of sequencing data was produced from each parental line. Reference genome-guided mapping and SNP calling revealed 674,521 SNPs between the two cabbage lines, with an average of one SNP per 662.5 bp. Among 167 dCAPS markers derived from candidate SNPs, 117 (70.1%) were validated as bona fide SNPs showing polymorphism between the parental lines. We then improved the resolution of a previous genetic map by adding 103 markers including 87 SNP-based dCAPS markers. The new map composed of 368 markers and covers 1467.3 cM with an average interval of 3.88 cM between adjacent markers. We evaluated black rot resistance in the mapping population in three independent inoculation tests using F2:3 progenies and identified one major QTL and three minor QTLs.ConclusionWe report successful utilization of whole-genome resequencing for large-scale SNP identification and development of molecular markers for genetic map construction. In addition, we identified novel QTLs for black rot resistance. The high-density genetic map will promote QTL analysis for other important agricultural traits and marker-assisted breeding of B. oleracea.Electronic supplementary materialThe online version of this article (doi:10.1186/s12870-015-0424-6) contains supplementary material, which is available to authorized users.

Identification of Differentially Expressed Genes During Pseudomonas fluorescens Mediated Systemic Resistance in Cabbage

The study of microbial ecology and the microbial interactions with plants provides an insight into the biocontrol of plant diseases using antagonistic microbes. Pseudomonas fluorescens was used as a biological control agent against black rot disease caused by Xanthomonas campestris pv. campestris. The Suppression subtractive hybridization (SSH) was used to elucidate the differentially expressed genes in cabbage (Brassica oleracea var. capitata) upon the application of Pseudomonas fluorescens. A total of 140 expressed sequence tags (EST) were obtained. The analyses of these ESTs showed that many defense related genes like peroxidase, heat shock proteins, were upregulated. Many transcripts related to signalling pathways and pathogen recognition were identified. The important finding of the study is the identification of the unigene belonging to the SWEET protein family in cabbage. The study also resulted in the identification of 10 unigenes which possibly depict the interaction of Pseudomonas fluorescens in combating disease. These unigenes have been submitted to dbEST. The results show that those genes which are upregulated during pathogen attack are also induced upon application of Pseudomonas fluorescens indicating the possible mechanism of systemic resistance induced by P. fluorescens to combat disease.

Host plant resistance towards the cabbage whitefly in Brassica oleracea and its wild relatives

The cabbage whitefly (Aleyrodes proletella) is a phloem-feeding insect that is a serious problem in Brassica oleracea crops like Brussels sprouts, kale and savoy cabbage. In order to develop whitefly-resistant varieties it is essential to identify effective sources of resistance. In this study, we screened a large collection of 432 accessions, including wild material and landraces of Brassica oleracea as well as crop wild relatives, to determine whitefly performance in a no-choice field experiment. Putatively resistant accessions were further tested under greenhouse conditions. Resistant accessions were identified among B. oleracea var. capitata (cabbage) landraces and in the species B. villosa, B. incana and B. montana. Whereas resistance in cabbage is only expressed in plants of at least 12 weeks old, some wild relatives were already starting to express resistance at 6 weeks. This could open up possibilities for breeding cabbages that are resistant at a young(er) plant age. Our research also shows again the importance of crop wild relatives for finding pest resistances.

Leaf epicuticular wax as a factor of antixenotic resistance of cabbage to cabbage flea beetles and cabbage stink bugs attack

The aim of present research was to establish the role of epicuticular wax content in eight cabbage genotypes (four white hybrids and one red hybrid, two red varieties and one white variety) in the context of its natural resistance to attack cabbage flea beetles (Phyllotreta spp.) and cabbage stink bugs (Eurydema spp.), which are among the most important cabbage pests in southern Europe. For this reason and for the purpose of diminishing the use of synthetic insecticides against the cabbage pests the field experiments in 2006 and 2008 were conducted. We found out that individual cabbage genotypes – they had different epicuticular wax content – differ in regard to their susceptibility to attacks by the studied groups of harmful insect pests. The highest susceptibility to attacks by Phyllotreta spp. was confirmed for the hybrid ‘Cheers F1’, in the first year (1.68 ± 0.05), as well as in the second year of the experiment (2.87 ± 0.13). Cabbage stink bugs in both years of the experiment caused the highest extent of injuries on the hybrids ‘Destiny F1’, ‘Cheers F1’, and ‘Vestri F1’. In both years we found higher epicuticular wax content in red cabbage genotypes. In almost all studied genotypes we found a pronounced negative correlation between the content of epicuticular wax and the extent of injuries done by both groups of harmful pests. We have established that epicuticular wax is an important factor of cabbage's antixenotic resistance to attacks by cabbage flea beetles and cabbage stink bugs, and that the cabbage genotypes with higher content of this substance are consequently more suitable for environmentally acceptable manners of cabbage production.

Quantity of glucosinolates in 10 cabbage genotypes and their impact on the feeding of Mamestra brassicae caterpillars

In 2011, we studied the glucosinolate content in 5 cultivars and 5 cabbage hybrids grown outdoors in order to study their influence on the feeding of cabbage moth caterpillars (Mamestra brassicae). The selected genotypes were categorized into three groups, early (the growth period from 55 to 70 days), mid-early (80-90 days) and mid-late (110-140 days), while the samples of cabbage for glucosinolate analysis were taken at five intervals, during which we also assessed genotypes for the extent of damage caused by caterpillars. We found that the feeding of caterpillars affected primarily the mid-early and mid-late genotypes of cabbage, and that the glucosinolate content among the different cabbage genotypes varies. The highest content of the analyzed glucosinolates was established in mid-late genotypes. Glucobrassicin was the only glucosinolate found in all cabbage genotypes, yet its antixenotic effect (r=0.20) was very low. We found that sinalbin negatively affects the feeding of cabbage moth caterpillars in mid-early cabbage genotypes (r=-0.34), while the same effect of sinigrin on the extent of damage can be observed in mid-late genotypes (r=-0.27). We have established a strong or moderate correlation between the gluconapin (r=0.87) and progoitrin (r=0.66) contents in mid-late genotypes and the extent of damage caused by caterpillars. Our research proves that different cabbage genotypes are responsible for different susceptibilities to damage by the cabbage moth, and that one of the factors of natural resistance of cabbage are also glucosinolates. Despite this, due to their variability in cabbage we cannot precisely determine the set of genotypes that would ensure a higher cabbage yield as a result of less damage caused by the cabbage moth. Thus, we need to identify in more detail the reasons for the time and quantum variability of glucosinolates in Brassicaceae.

Infection of Plasmodiophora brassicae in Chinese cabbage.

Brassica crops infected by Plasmodiophora brassicae can produce root galls (clubroots) and be prevented from growing normally. To understand the series of changes that occur in the host root during root gall production, the resistance character of 21 Chinese cabbage lines were identified and then resistant and susceptible lines were used for infection observation. Hydroponic technology system was used for plants growing, and the infection process of P. brassicae in the roots of resistant and susceptible Chinese cabbage was examined based on morphology and microscopic characteristics using micoscope. In susceptible Chinese cabbage, the root hair infection stage occurred over approximately 7 days after inoculation, the cortical infection happened over approximatly 14 days after inoculation, and clubroots formed in approximately 30 days after inoculation. However, in resistant Chinese cabbage, the pathogen could be prevented and maintained in the root hair infection stage. This research provides a foundation for the subsequent studies of cabbage resistance of P. brassicae.

Does Epidermal Thickness Influence White Cabbage Resistance against Onion Thrips (<i>Thrips tabaci</i>)?

Present studies were made to investigate the association between epidermal thickness and resistance of white cabbage against onion thrips, Thrips tabaci Lindeman, 1889 (Thysanoptera: Thripidae). Six white cabbage varieties including three susceptible (‘Green Gem’, ‘Hurricane’ and ‘Quisor’) and three resistant to onion thrips (‘Balashi’, ‘Bloktor’ and ‘Riana’) were involved in the studies. Additionally, the extent of antixenotic resistance during head formation and the level of thrips damage at harvest were also assessed and compared between varieties. A higher density of onion thrips was observed on susceptible than on resistant varieties. The results indicate that the epidermis is of the same thickness in susceptible white cabbage varieties as in resistant ones; therefore, we conclude that the thicknesses of either the adaxial or the abaxial part of the epidermis of head-forming leaves is not responsible for cabbage resistance to thrips. The study thus confirms that antixenotic resistance of white cabbage to thrips is not determined by epidermal thickness.

Antixenotic Resistance of Cabbage to Onion Thrips (Thysanoptera: Thripidae). I. Light Reflectance

Onion thrips (Thrips tabaci Lindeman) has become a significant pest of cabbage (Brasssica oleracea L.) in regions with a dry continental climate. Thrips-resistant cabbage varieties have been developed in breeding programs, but the mechanisms ofresistance remain largely unknown. Antixenosis, one of the three resistance mechanisms, may play a role but no plant trait has been identified as a source of antixenosis. A series of studies were conducted to identify resistance mechanisms in this insect- crop interaction and to seek plant traits that were correlated to resistance. In this first article of the series, the result of studying antixenosis and overall resistance of cabbage and the correlation between antixenosis and light reflectance characteristics are reported. There were distinct differences in the overall resistance to thrips between the six cabbage varieties studied. There were more pronounced differences between varieties based on the number of damaged head leaves compared with the use of damage ratings as a measure of overall resistance. Varieties also differed in their level of antixenosis; proportional abundance of thrips adults on head-forming leaves was more closely correlated to overall resistance of cabbage than actual thrips numbers. Some of the variables computed from the recorded reflectance spectra of cabbage were correlated to thrips abundance on head-forming leaves only in the first but not in the second year of this study, suggesting that either spectral characteristics do not affect antixenosis or other variables may affect thrips' responses to spectral cues. Furthermore, multiple spray applications of a kaolin particle-based product significantly changed the light reflectance characteristics of cabbage, but it did not reduce the actual thrips abundance on head-forming leaves.

Development of InDel markers linked to Fusarium wilt resistance in cabbage

Cabbage Fusarium wilt (CFW) is a destructive disease causing great losses to cabbage (Brassica oleracea L. var. capitata L.) production worldwide. At present, there are few reports concerning molecular marker research on cabbage resistance to CFW. In this study, 160 double haploid (DH) lines were obtained from the F1 population of a 99–77 (highly resistant to CFW) × 99–91 (highly susceptible to CFW) cross. Insertion–deletion (InDel) markers were designed according to the reference genome sequence of cabbage and the whole-genome re-sequencing data of the two parents. A genetic map of chromosome C06 including seven InDel markers was constructed based on the DH population. Thus, FOC (resistance gene to Fusarium oxysporum f. sp. conglutinans) was located on chromosome C06 and two InDel markers out of the seven, M10 and A1, flanked the gene at 1.2 and 0.6 cM, respectively. Marker A1 revealed a significant consistency with the phenotype assay in the F2 population as well as in 40 inbred lines (96 and 82 %, respectively). This study lays the foundation for fine mapping and cloning of the FOC gene and for marker-assisted selection in cabbage resistance breeding.