Transcriptome analysis of Brassica juncea var. tumida Tsen responses to Plasmodiophora brassicae primed by the biocontrol strain Zhihengliuella aestuarii
文献类型: 外文期刊
作者:
Luo, Yuanli
1
;
Dong, Daiwen
2
;
Su, Yu
2
;
Wang, Xuyi
2
;
Peng, Yumei
2
;
Peng, Jiang
2
;
Zhou, Changyong
1
;
作者机构: 1.Southwest Univ, Chinese Acad Agr Sci, Citrus Res Inst, Chongqing 400712, Peoples R China
2.Southeast Chongqing Acad Agr Sci, Chongqing 408000, Peoples R China
3.Chongqing Univ, Key Lab Gene Funct & Regulat Chongqing, Bioengn Coll, Chongqing 40030, Peoples R China
关键词: Brassica juncea var. tumida Tsen; Transcriptome; Differentially expressed genes; Plasmodiophora brassicae; Resistant genes; Zhihengliuella aestuarii
期刊名称:FUNCTIONAL & INTEGRATIVE GENOMICS ( 影响因子:3.41; 五年影响因子:3.616 )
ISSN: 1438-793X
年卷期: 2018 年 18 卷 3 期
页码:
收录情况: SCI
摘要:
Mustard clubroot, caused by Plasmodiophora brassicae, is a serious disease that affects Brassica juncea var. tumida Tsen, a mustard plant that is the raw material for a traditional fermented food manufactured in Chongqing, China. In our laboratory, we screened the antagonistic bacteria Zhihengliuella aestuarii against P. brassicae. To better understand the biocontrol mechanism, three transcriptome analyses of B. juncea var. tumida Tsen were conducted using Illumina HiSeq 4000, one from B. juncea only inoculated with P. brassicae (P), one inoculated with P. brassica and the biocontrol agent Z. aestuarii at the same time (P + B), and the other was the control (H), in which P. brassicae was replaced by sterile water. A total of 19.94 Gb was generated by Illumina HiSeq sequencing. The sequence data were de novo assembled, and 107,617 unigenes were obtained. In total, 5629 differentially expressed genes between biocontrol-treated (P + B) and infected (P) samples were assigned to 126 KEGG pathways. Using multiple testing corrections, 20 pathways were significantly enriched with Qvalue ae
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