Wu Guichun, Zhang Yuqiang, Wang Bo, Li Kaihuai, Lou Yuanlai, Zhao Yancun, Liu Fengquan
Jiangsu Key Laboratory for Food Quality and Safety-State Key Laboratory Cultivation Base of Ministry of Science and Technology, Institute of Plant Protection, Jiangsu Academy of Agricultural Sciences, No. 50 Zhongling Street, Nanjing, Jiangsu, 210014, P. R. China.
State Key Laboratory of Microbial Technology, Marine Biotechnology Research Center, Shandong University, Qingdao, 266237, P. R. China.
Rice (N Y). 2021 Jun 26;14(1):57. doi: 10.1186/s12284-021-00503-x.
Xanthomonas oryzae pv. oryzae (Xoo) causes bacterial leaf blight, a devastating rice disease. The Xoo-rice interaction, wherein wide ranging host- and pathogen-derived proteins and genes wage molecular arms race, is a research hotspot. Hence, the identification of novel rice-induced Xoo virulence factors and characterization of their roles affecting rice global gene expression profiles will provide an integrated and better understanding of Xoo-rice interactions from the molecular perspective.
Using comparative proteomics and an in vitro interaction system, we revealed that 5 protein spots from Xoo exhibited significantly different expression patterns (|fold change| > 1.5) at 3, 6, 12 h after susceptible rice leaf extract (RLX) treatment. MALDI-TOF MS analysis and pathogenicity tests showed that 4 host-induced proteins, including phosphohexose mutase, inositol monophosphatase, arginase and septum site-determining protein, affected Xoo virulence. Among them, mutants of two host-induced carbohydrate metabolism enzyme-encoding genes, ΔxanA and Δimp, elicited enhanced defense responses and nearly abolished Xoo virulence in rice. To decipher rice differentially expressed genes (DEGs) associated with xanA and imp, transcriptomic responses of ΔxanA-treated and Δimp-treated susceptible rice were compared to those in rice treated with PXO99 at 1 and 3 dpi. A total of 1521 and 227 DEGs were identified for PXO99 vs Δimp at 1 and 3 dpi, while for PXO99 vs ΔxanA, there were 131 and 106 DEGs, respectively. GO, KEGG and MapMan analyses revealed that the DEGs for PXO99 vs Δimp were mainly involved in photosynthesis, signal transduction, transcription, oxidation-reduction, hydrogen peroxide catabolism, ion transport, phenylpropanoid biosynthesis and metabolism of carbohydrates, lipids, amino acids, secondary metabolites, hormones, and nucleotides, while the DEGs from PXO99 vs ΔxanA were predominantly associated with photosynthesis, signal transduction, oxidation-reduction, phenylpropanoid biosynthesis, cytochrome P450 and metabolism of carbohydrates, lipids, amino acids, secondary metabolites and hormones. Although most pathways were associated with both the Δimp and ΔxanA treatments, the underlying genes were not the same.
Our study identified two novel host-induced virulence factors XanA and Imp in Xoo, and revealed their roles in global gene expression in susceptible rice. These results provide valuable insights into the molecular mechanisms of pathogen infection strategies and plant immunity.
水稻白叶枯病菌(Xanthomonas oryzae pv. oryzae,Xoo)引起细菌性条斑病,这是一种毁灭性的水稻病害。Xoo与水稻的相互作用是一个研究热点,在这种相互作用中,宿主和病原体来源的多种蛋白质和基因展开了分子军备竞赛。因此,鉴定新的水稻诱导的Xoo毒力因子并表征它们对水稻全局基因表达谱的影响,将从分子角度为Xoo与水稻的相互作用提供更全面和深入的理解。
利用比较蛋白质组学和体外相互作用系统,我们发现,在感病水稻叶片提取物(RLX)处理后3、6、12小时,Xoo的5个蛋白点表现出显著不同的表达模式(|倍数变化|>1.5)。基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)分析和致病性测试表明,4种宿主诱导蛋白,包括磷酸己糖异构酶、肌醇单磷酸酶、精氨酸酶和隔膜位点决定蛋白,影响Xoo的毒力。其中,两个宿主诱导的碳水化合物代谢酶编码基因ΔxanA和Δimp的突变体引发了增强的防御反应,并几乎消除了Xoo在水稻中的毒力。为了解析与xanA和imp相关的水稻差异表达基因(DEG),将ΔxanA处理和Δimp处理的感病水稻在接种后1天和3天的转录组反应与PXO99处理的水稻进行了比较。在接种后1天和3天,PXO99与Δimp相比分别鉴定出1521个和227个DEG,而PXO99与ΔxanA相比分别有131个和106个DEG。基因本体(GO)、京都基因与基因组百科全书(KEGG)和MapMan分析表明,PXO99与Δimp的DEG主要参与光合作用、信号转导、转录、氧化还原、过氧化氢分解代谢、离子运输、苯丙烷生物合成以及碳水化合物、脂质、氨基酸、次生代谢物、激素和核苷酸的代谢,而PXO99与ΔxanA的DEG主要与光合作用、信号转导、氧化还原、苯丙烷生物合成、细胞色素P450以及碳水化合物、脂质、氨基酸、次生代谢物和激素的代谢相关。虽然大多数途径与Δimp和ΔxanA处理都有关,但相关基因并不相同。
我们的研究在Xoo中鉴定出两种新的宿主诱导毒力因子XanA和Imp,并揭示了它们在感病水稻全局基因表达中的作用。这些结果为病原体感染策略和植物免疫的分子机制提供了有价值的见解。