Soni Pooja, Nayak Spurthi N, Kumar Rakesh, Pandey Manish K, Singh Namita, Sudini Hari K, Bajaj Prasad, Fountain Jake C, Singam Prashant, Hong Yanbin, Chen Xiaoping, Zhuang Weijian, Liao Boshou, Guo Baozhu, Varshney Rajeev K
Center of Excellence in Genomics & Systems Biology (CEGSB), International Crops Research Institute for the Semi-Arid Tropics (ICRISAT), Hyderabad 502324, India.
Department of Genetics, Osmania University, Hyderabad 500007, India.
J Fungi (Basel). 2020 Dec 16;6(4):370. doi: 10.3390/jof6040370.
Aflatoxin-affected groundnut or peanut presents a major global health issue to both commercial and subsistence farming. Therefore, understanding the genetic and molecular mechanisms associated with resistance to aflatoxin production during host-pathogen interactions is crucial for breeding groundnut cultivars with minimal level of aflatoxin contamination. Here, we performed gene expression profiling to better understand the mechanisms involved in reduction and prevention of aflatoxin contamination resulting from infection in groundnut seeds. RNA sequencing (RNA-Seq) of 16 samples from different time points during infection (24 h, 48 h, 72 h and the 7th day after inoculation) in U 4-7-5 (resistant) and JL 24 (susceptible) genotypes yielded 840.5 million raw reads with an average of 52.5 million reads per sample. A total of 1779 unique differentially expressed genes (DEGs) were identified. Furthermore, comprehensive analysis revealed several pathways, such as disease resistance, hormone biosynthetic signaling, flavonoid biosynthesis, reactive oxygen species (ROS) detoxifying, cell wall metabolism and catabolizing and seed germination. We also detected several highly upregulated transcription factors, such as ARF, DBB, MYB, NAC and C2H2 in the resistant genotype in comparison to the susceptible genotype after inoculation. Moreover, RNA-Seq analysis suggested the occurrence of coordinated control of key pathways controlling cellular physiology and metabolism upon infection, resulting in reduced aflatoxin production.
受黄曲霉毒素影响的花生对商业种植和自给农业来说都是一个重大的全球健康问题。因此,了解宿主-病原体相互作用过程中与黄曲霉毒素产生抗性相关的遗传和分子机制,对于培育黄曲霉毒素污染水平最低的花生品种至关重要。在此,我们进行了基因表达谱分析,以更好地理解花生种子感染后减少和预防黄曲霉毒素污染所涉及的机制。对U 4-7-5(抗性)和JL 24(敏感)基因型在感染期间(接种后24小时、48小时、72小时和第7天)不同时间点的16个样本进行RNA测序(RNA-Seq),共获得8.405亿条原始读数,平均每个样本5250万条读数。总共鉴定出1779个独特的差异表达基因(DEG)。此外,综合分析揭示了几个途径,如抗病性、激素生物合成信号传导、类黄酮生物合成、活性氧(ROS)解毒、细胞壁代谢和分解以及种子萌发。我们还检测到,与接种后的敏感基因型相比,抗性基因型中有几个转录因子高度上调,如ARF、DBB、MYB、NAC和C2H2。此外,RNA-Seq分析表明,感染后控制细胞生理和代谢的关键途径存在协同调控,从而减少了黄曲霉毒素的产生。