Wang Li, Zhang Weixi, Shen Wanna, Li Min, Fu Yuchen, Li Zheng, Li Jinxin, Liu Huixiang, Su Xiaohua, Zhang Bingyu, Zhao Jiaping
State Key Laboratory of Tree Genetics and Breeding, Research Institute of Forestry, Chinese Academy of Forestry, Beijing, China.
State Key Laboratory of Tree Genetics and Breeding, Institute of Ecological Conservation and Restoration, Chinese Academy of Forestry, Beijing, China.
Front Plant Sci. 2023 Jun 15;14:1163232. doi: 10.3389/fpls.2023.1163232. eCollection 2023.
Recently, a novel poplar mosaic disease caused by bean common mosaic virus (BCMV) was investigated in var. in China. Symptom characteristics, physiological performance of the host, histopathology, genome sequences and vectors, and gene regulation at the transcriptional and posttranscriptional levels were analyzed and RT-qPCR (quantitative reverse transcription PCR) validation of expression was performed in our experiments. In this work, the mechanisms by which the BCMV pathogen impacts physiological performance and the molecular mechanisms of the poplar response to viral infection were reported. The results showed that BCMV infection decreased the chlorophyll content, inhibited the net photosynthesis rate (Pn) and stomatal conductance (Gs), and significantly changed chlorophyll fluorescence parameters in diseased leaves. Transcriptome analysis revealed that the expression of the majority of DEGs (differentially expressed genes) involved in the flavonoid biosynthesis pathway was promoted, but the expression of all or almost all DEGs associated with photosynthesis-antenna proteins and the photosynthesis pathway was inhibited in poplar leaves, suggesting that BCMV infection increased the accumulation of flavonoids but decreased photosynthesis in hosts. Gene set enrichment analysis (GSEA) illustrated that viral infection promoted the expression of genes involved in the defense response or plant-pathogen interaction. MicroRNA-seq analysis illustrated that 10 miRNA families were upregulated while 6 families were downregulated in diseased poplar leaves; moreover, miR156, the largest family with the most miRNA members and target genes, was only differentially upregulated in long-period disease (LD) poplar leaves. Integrated transcriptome and miRNA-seq analyses revealed 29 and 145 candidate miRNA-target gene pairs; however, only 17 and 76 pairs, accounting for 2.2% and 3.2% of all DEGs, were authentically negatively regulated in short-period disease (SD) and LD leaves, respectively. Interestingly, 4 miR156/SPL (squamosa promoter-binding-like protein) miRNA-target gene pairs were identified in LD leaves: the miR156 molecules were upregulated, but SPL genes were downregulated. In conclusion, BCMV infection significantly changed transcriptional and posttranscriptional gene expression in poplar leaves, inhibited photosynthesis, increased the accumulation of flavonoids, induced systematic mosaic symptoms, and decreased physiological performance in diseased poplar leaves. This study elucidated the fine-tuned regulation of poplar gene expression by BCMV; moreover, the results also suggested that miR156/SPL modules played important roles in the virus response and development of viral systematic symptoms in plant virus disease.
最近,在中国对一种由菜豆普通花叶病毒(BCMV)引起的新型杨树花叶病进行了调查。在我们的实验中,分析了症状特征、寄主的生理表现、组织病理学、基因组序列与载体,以及转录和转录后水平的基因调控,并进行了表达的RT-qPCR(定量逆转录PCR)验证。在这项工作中,报道了BCMV病原体影响生理表现的机制以及杨树对病毒感染的分子反应机制。结果表明,BCMV感染降低了叶绿素含量,抑制了净光合速率(Pn)和气孔导度(Gs),并显著改变了病叶中的叶绿素荧光参数。转录组分析显示,参与黄酮类生物合成途径的大多数差异表达基因(DEG)的表达被促进,但杨树叶片中与光合天线蛋白和光合作用途径相关的所有或几乎所有DEG的表达均受到抑制,这表明BCMV感染增加了寄主中黄酮类化合物的积累,但降低了光合作用。基因集富集分析(GSEA)表明,病毒感染促进了参与防御反应或植物-病原体相互作用的基因的表达。微小RNA测序分析表明,病杨树叶中有10个微小RNA家族上调,6个家族下调;此外,miR156是成员和靶基因最多的最大家族,仅在长期病害(LD)杨树叶中差异上调。综合转录组和微小RNA测序分析揭示了29个和145个候选微小RNA-靶基因对;然而,在短期病害(SD)和LD叶片中,分别只有17对和76对,占所有DEG的2.2%和3.2%,受到真正的负调控。有趣的是,在LD叶片中鉴定出4个miR156/SPL(类鳞状启动子结合蛋白)微小RNA-靶基因对:miR156分子上调,但SPL基因下调。总之,BCMV感染显著改变了杨树叶中的转录和转录后基因表达,抑制了光合作用,增加了黄酮类化合物的积累,诱导了系统花叶症状,并降低了病杨树叶的生理表现。本研究阐明了BCMV对杨树基因表达的精细调控;此外,结果还表明miR156/SPL模块在植物病毒病的病毒反应和病毒系统症状发展中发挥了重要作用。