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Detection of Clubroot Disease Resistance in Brassica juncea Germplasm at the Seedling Stage

Authors :
Wenlong Yang
Jiangping Song
Xiaohui Zhang
Chu Xu
Jiaqi Han
Zhijie Li
Yang Wang
Huixia Jia
Haiping Wang
Source :
Agronomy, Vol 14, Iss 9, p 2042 (2024)
Publication Year :
2024
Publisher :
MDPI AG, 2024.

Abstract

Infection by the mustard clubroot disease pathogen Plasmodiophora brassicae has a significant negative impact on the quality and yield of Chinese mustard (Brassica juncea). At present, screening resistant resources for breeding programs is the most economical and effective method available to control this disease. In this study, we isolated P. brassicae physiological race 4 from Chinese cabbage and examined 483 mustard germplasm resources (193 leaf mustard, 96 stem mustard, and 194 root mustard) from China and abroad to identify resistance to clubroot disease at the seedling stage through irrigation inoculation with the isolated pathogen. The results showed that there were no immune varieties among the tested mustard germplasm, but that there were differences in resistance to clubroot disease among the three mustard types. More than 90% of leaf and stem mustard resources were susceptible to clubroot disease, whereas 38.66% of root mustard resources showed resistance. In total, we detected 4 highly resistant, 9 resistant, and 83 moderately resistant varieties, of which 4 highly resistant, 8 resistant, and 63 moderately resistant varieties were root mustard resources, whereas only 1 resistant and 5 moderately resistant varieties were stem mustard resources, and 15 moderately resistant varieties were leaf mustard resources. In addition, we used seven molecular markers for clubroot disease resistance in Chinese cabbage to detect stem and root mustard resources. The results showed that the marker CRk was detected in 97.87% of stem mustard and 92.49% of root mustard resources. Six markers (Crr1, Crr2, Crr3, CRa, CRb, and CRc) were detected in 18.09%, 7.45%, 2.13%, 6.38%, 12.77%, and 12.77% of stem mustard germplasms, and four markers (Crr1, Crr2, Crr3, and CRc) were detected in 8.09%, 8.67%, 10.40%, and 8.67% of root mustard germplasms, respectively, suggesting that these markers are not suitable for detecting mustard germplasm resistance to clubroot disease. This study provides a technical reference and material support for the breeding of mustard varieties resistant to clubroot disease.

Details

Language :
English
ISSN :
14092042 and 20734395
Volume :
14
Issue :
9
Database :
Directory of Open Access Journals
Journal :
Agronomy
Publication Type :
Academic Journal
Accession number :
edsdoj.43ba61879a420ba3284678f7783a27
Document Type :
article
Full Text :
https://doi.org/10.3390/agronomy14092042