Ahmed Reshma, Dey Kuntal Kumar, Senthil-Kumar Muthappa, Modi Mahendra Kumar, Sarmah Bidyut Kumar, Bhorali Priyadarshini
Department of Agricultural Biotechnology, Assam Agricultural University, Jorhat, Assam, India.
National Institute of Plant Genome Research, New Delhi, India.
Front Plant Sci. 2024 Jan 18;14:1251349. doi: 10.3389/fpls.2023.1251349. eCollection 2023.
Alternaria blight is a devastating disease that causes significant crop losses in oilseed Brassicas every year. Adoption of conventional breeding to generate disease-resistant varieties has so far been unsuccessful due to the lack of suitable resistant source germplasms of cultivated spp. A thorough understanding of the molecular basis of resistance, as well as the identification of defense-related genes involved in resistance responses in closely related wild germplasms, would substantially aid in disease management. In the current study, a comparative transcriptome profiling was performed using Illumina based RNA-seq to detect differentially expressed genes (DEGs) specifically modulated in response to infection in resistant , a close relative of Brassicas, and the highly susceptible . The analysis revealed that, at 48 hpi (hours post inoculation), 3396 genes were upregulated and 23239 were downregulated, whereas at 72 hpi, 4023 genes were upregulated and 21116 were downregulated. Furthermore, a large number of defense response genes were detected to be specifically regulated as a result of Alternaria infection. The transcriptome data was validated using qPCR-based expression profiling for selected defense-related DEGs, that revealed significantly higher fold change in gene expression in when compared to . Expression of most of the selected genes was elevated across all the time points under study with significantly higher expression towards the later time point of 72 hpi in the resistant germplasm. activates a stronger defense response reaction against the disease by deploying an array of genes and transcription factors involved in a wide range of biological processes such as pathogen recognition, signal transduction, cell wall modification, antioxidation, transcription regulation, etc. Overall, the study provides new insights on resistance of against , which will aid in devising strategies for breeding resistant varieties of oilseed Brassica.
链格孢叶枯病是一种毁灭性病害,每年都会给油菜籽作物造成重大损失。由于缺乏栽培种合适的抗病源种质,采用常规育种培育抗病品种至今尚未成功。深入了解抗性的分子基础,以及鉴定密切相关野生种质中参与抗性反应的防御相关基因,将极大地有助于病害管理。在本研究中,利用基于Illumina的RNA测序进行了比较转录组分析,以检测在油菜近缘种抗性材料和高感材料中因感染链格孢而特异性调控的差异表达基因(DEG)。分析表明,在接种后48小时(hpi),3396个基因上调,23239个基因下调;而在72 hpi时,4023个基因上调,21116个基因下调。此外,检测到大量防御反应基因因链格孢感染而受到特异性调控。利用基于qPCR的选定防御相关DEG表达谱对转录组数据进行了验证,结果显示与相比,基因表达的倍数变化显著更高。在研究的所有时间点,大多数选定基因的表达均有所升高,在抗性种质中72 hpi的后期时间点表达显著更高。通过部署一系列参与广泛生物过程(如病原体识别、信号转导、细胞壁修饰、抗氧化、转录调控等)的基因和转录因子,激活了针对该病害更强的防御反应。总体而言,该研究为油菜对链格孢的抗性提供了新的见解,这将有助于制定培育油菜抗病品种的策略。