Basim Huseyin, Basim Esin, Tombuloglu Huseyin, Unver Turgay
Department of Plant Protection, Faculty of Agriculture, Akdeniz University, 07070 Antalya, Turkey.
Department of Organic Agriculture, Technical Sciences Vocational School, Akdeniz University, 07070 Antalya, Turkey.
Genomics. 2021 Jul;113(4):2455-2467. doi: 10.1016/j.ygeno.2021.05.033. Epub 2021 May 28.
Clavibacter michiganensis subsp. michiganensis (Cmm) is a gram-positive bacterium causing destructive bacterial wilt and canker disease in tomato. Herein, a comparative transcriptome analysis was performed on Cmm-resistant and -susceptible tomato lines. Tomato seedlings were inoculated with Cmm and harvested for transcriptome analysis after 4 and 8 day time-points. Twenty-four transcriptome libraries were profiled by RNA sequencing approach. Total of 545 million clean reads was generated. 1642 and 2715 differentially expressed genes (DEG) were identified in susceptible lines within 4 and 8 days after inoculation (DAI), respectively. In resistant lines, 1731 and 1281 DEGs were found following 4 and 8 DAI, respectively. Gene Ontology analysis resulted in a higher number of genes involved in biological processes and molecular functions in susceptible lines. On the other hand, such biological processes, "defense response", and "response to stress" were distinctly indicated in resistant lines which were not found in susceptible ones upon inoculation, according to the gene set enrichment analyses. Upon Cmm-inoculation, several defense responsive genes were found to be differentially expressed. Of which 26 genes were in the resistant line and three were in the susceptible line. This study helps to understand the transcriptome response of Cmm-resistant and -susceptible tomato lines. The results provide comprehensive data for molecular breeding studies, for the purpose to control of the pathogen in tomato.
密执安棒杆菌密执安亚种(Cmm)是一种革兰氏阳性细菌,可导致番茄毁灭性的青枯病和溃疡病。在此,对番茄抗Cmm和感Cmm品系进行了比较转录组分析。用Cmm接种番茄幼苗,并在4天和8天时间点后收获进行转录组分析。通过RNA测序方法对24个转录组文库进行了分析。共产生了5.45亿条clean reads。在接种后4天和8天内,分别在感病品系中鉴定出1642个和2715个差异表达基因(DEG)。在抗病品系中,接种后4天和8天分别发现1731个和1281个DEG。基因本体分析表明,感病品系中参与生物过程和分子功能的基因数量更多。另一方面,根据基因集富集分析,在抗病品系中明显显示出“防御反应”和“应激反应”等生物过程,而在接种后的感病品系中未发现。接种Cmm后,发现几个防御反应基因差异表达。其中26个基因在抗病品系中,3个基因在感病品系中。本研究有助于了解番茄抗Cmm和感Cmm品系的转录组反应。研究结果为分子育种研究提供了全面的数据,旨在控制番茄中的病原菌。