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Seeding And Adult-Plant Resistance To Pomdery Mildew In Bread Wheat And QTL Analysis Of Pomdery Mildew Resistance In Bainong 64

Posted on:2006-10-26Degree:DoctorType:Dissertation
Country:ChinaCandidate:Z L WangFull Text:PDF
GTID:1103360155455844Subject:Crop Genetics and Breeding
Abstract/Summary:PDF Full Text Request
Powdery mildew is one of the major diseases in wheat. Resistant cultivars offer an effective, economical, and environmentally safe way to control powdery mildew. The adult-plant resistance (APR) shows moderately resistant to powdery mildew at adult plant stage by retarding infection, growth and reproduction of the pathogen, and more durable than race-specific resistance. The objectives of this study were to evaluate the effectiveness of some Pm-genes in China, identify genes that confer seedling resistance to powdery mildew in 35 Chinese bread wheat cultivars and 85 introductions used by breeding programs in China, and evaluate APR of 76 cultivars in the field. A genetic linkage map was constructed by using 218 F2:3 lines derived from the cross between a APR cultivar Bainong 64 and a powdery mildew susceptible cultivar Jingshuang16 and QTL analysis was performed. The results were presented below: 1. Genotypes carrying Pm12 and Pm16 were highly resistant to all powdery mildew isolates tested. Genotypes carrying Pm20, Pm2+6, Pm2+mld, Pm2+Ta, Pm4a, Pm4b and Pm4+8 were also effective to powdery mildew, whereas, those carrying Pm1, Pm3e, Pm5, Pm7, Pm3a, Pm3d, Pm3f, Pm6, Pm8 and Pm17 were susceptible to most powdery mildew isolates tested. 2. Totally, 42 out of 120 tested wheat cultivars and lines carried one or more resistance genes to powdery mildew. Thirty cultivars contained unknown Pm genes. There were 26 cultivars carrying Pm8 and its complex. Pm8 was the most common resistance gene, followed by Pm3d, Pm6, Pm4b and Pm2. 3. The frequency of 1B/1R translocation was 48% in the cultivars tested. All genotypes carrying Pm8 were 1B/1R translocation. However, only 29.4% and 51.2 of 1B/1R translocation lines showed the Pm8 reaction pattern in Chinese cultivars and introduction lines, respectively. 4. Twenty-five cultivars and lines showed APR to powdery mildew according to cluster analysis based on R1 (rate of ID), R2 (rate of severity on penultimate leaves), AUDPC (area under the disease progress curve), DI (disease index) and MDS(maximum disease severity on penultimate) and LSD analysis, in combination with the postulation of Pm genes at seedling stage. Thirteen lines were typical of APR that were susceptible to all powdery mildew isolates tested at seeding stage but moderately resistant to powdery mildew in adult plants. Twelve lines in which major-gene resistance has been overcome and showed moderately resistant to powdery mildew in adult plant. 5. APR lines were characterized with lower AUDPC and MSD (between 11.9 to 99.7 and 1.0% to 8.0%, respectively) in comparsion with highly susceptible check cultivar Jingshuang 16 (AUDPC and MDS was 913.5 and 95.0%, respectively). They showed little conidia production, small colony size, and low disease severity. Results for APR identification based on MDS were siminar to the combined cluster analysis based on R1, R2, AUDPC, DI and MDS. Therefore, MDS was a simple parameter for APR identification. 6. A total of 158 markers including 100 SSRs and 58 AFLPs were mapped on 20 linkage groups covering 3114 cM, with an average distance of 19.7 cM. Twelve SSR markers unmapped previously were placed onto the genetic linkage map. 7. Five QTL named QPm-2B, QPm-2D, QPm-5A, QPm-7A and QPm-7D, respectively were associated with APR. The QTL QPm-2B, QPm-2D and QPm-7D explained 20%~21.3%, 15.5%~18% and 27.7%~28% of phenotypic variance, respectively. Two minor QTL QPm-5A and QPm-7A accounted for 7.5%~10.7% and 5.4%~6% of phenotypic variance, respectively. QTL associated with APR showed mainly additive effect. The negative additive value indicated that the QTL was from Bainong 64 conferring resistance to powdery mildew.
Keywords/Search Tags:Bread Wheat (Triticum aestivum L.), Powdery mildew, Pm gene, Adult plant resistance, QTL analysis
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