Chen Na, Yu Bingwei, Dong Riyue, Lei Jianjun, Chen Changming, Cao Bihao
College of Horticulture, South Agricultural University, Guangzhou City 510642, PR China; Key Laboratory of Biology and Germplasm Enhancement of Horticultural Crops in South China, Ministry of Agriculture, PR China.
College of Horticulture, South Agricultural University, Guangzhou City 510642, PR China; Key Laboratory of Biology and Germplasm Enhancement of Horticultural Crops in South China, Ministry of Agriculture, PR China.
Gene. 2018 Feb 20;644:137-147. doi: 10.1016/j.gene.2017.11.003. Epub 2017 Nov 3.
Eggplant (Solanum melongena) is a major vegetable crop worldwide. However, it is susceptible to bacterial wilt (BW) caused by Ralstonia solanacearum, which has become an important factor limiting eggplant yield and quality. The underlying mechanism of BW remains unknown. Here, RNA-sequencing was used to characterize the transcriptomes of resistant (R) and susceptible (S) strains before (R0, S0) and after (R1, S1) R. solanacearum inoculation. After the removal of low-quality sequences and assembly, 125,852 contigs, 122,508 transcripts, and 68,792 unigenes were identified, with 51,165 non-redundant unigenes annotated. Functional annotations were provided for 11,039 unigenes using four databases (NCBI Nr, Swissprot, KEGG and COG database). A total of 1137 and 9048 genes were found to be up- and down-regulated, respectively, in R0 relative to R1 samples, with 738 and 217 up- and down-regulated in S0 relative to R0 samples, 6087 and 5832 up- and down-regulated in S0 relative to S1 samples, and 4712 and 12,523 up- and down-regulated in S1 relative to R1 samples, respectively. In conclusion, our results provide useful insights into the potential mechanism of BW and are an important basis for further analysis.
茄子(茄属植物)是全球主要的蔬菜作物。然而,它易受青枯雷尔氏菌引起的青枯病影响,这已成为限制茄子产量和品质的重要因素。青枯病的潜在机制尚不清楚。在此,利用RNA测序来表征抗性(R)和感病(S)品系在接种青枯雷尔氏菌之前(R0、S0)和之后(R1、S1)的转录组。去除低质量序列并进行组装后,鉴定出125,852个重叠群、122,508个转录本和68,792个单基因,其中51,165个非冗余单基因得到注释。使用四个数据库(NCBI Nr、Swissprot、KEGG和COG数据库)为11,039个单基因提供了功能注释。相对于R1样本,R0中分别有1137个和9048个基因上调和下调;相对于R0样本,S0中有738个和217个基因上调和下调;相对于S1样本,S0中有6087个和5832个基因上调和下调;相对于R1样本,S1中有4712个和12,523个基因上调和下调。总之,我们的结果为青枯病的潜在机制提供了有用的见解,是进一步分析的重要基础。