Wang Zheng, Ma Lu-Yue, Cao Jun, Li Yu-Long, Ding Li-Na, Zhu Ke-Ming, Yang Yan-Hua, Tan Xiao-Li
Institute of Life Sciences, Jiangsu University, Zhenjiang, China.
Front Plant Sci. 2019 Oct 18;10:1314. doi: 10.3389/fpls.2019.01314. eCollection 2019.
(Lib.) de Bary is an unusual pathogen which has the broad host range, diverse infection modes, and potential double feeding lifestyles of both biotroph and necrotroph. It is capable of infecting over 400 plant species found worldwide and more than 60 names have agriculturally been used to refer to diseases caused by this pathogen. Plant defense to is a complex biological process and exhibits a typical quantitative disease resistance (QDR) response. Recent studies using and crop plants have obtained new advances in mechanisms used by plants to cope with infection. In this review, we focused on our current understanding on plant defense mechanisms against this pathogen, and set up a model for the defense process including three stages: recognition of this pathogen, signal transduction and defense response. We also have a particular interest in defense signaling mediated by diverse signaling molecules. We highlight the current challenges and unanswered questions in both the defense process and defense signaling. Essentially, we discussed candidate resistance genes newly mapped by using high-throughput experiments in important crops, and classified these potential gene targets into different stages of the defense process, which will broaden our understanding of the genetic architecture underlying quantitative resistance to . We proposed that more powerful mapping population(s) will be required for accurate and reliable QDR gene identification.
(里氏)德巴利氏菌是一种不寻常的病原体,具有广泛的宿主范围、多样的感染模式以及兼具活体营养型和死体营养型的潜在双重取食生活方式。它能够感染全球范围内发现的400多种植物物种,在农业上有60多个名称用于指代由这种病原体引起的疾病。植物对其的防御是一个复杂的生物学过程,并表现出典型的数量抗病性(QDR)反应。最近使用该菌和农作物进行的研究在植物应对该菌感染所采用的机制方面取得了新进展。在本综述中,我们聚焦于目前对植物针对这种病原体的防御机制的理解,并建立了一个防御过程模型,包括三个阶段:对这种病原体的识别、信号转导和防御反应。我们还特别关注由多种信号分子介导的防御信号传导。我们强调了防御过程和防御信号传导中当前面临的挑战和未解决的问题。本质上,我们讨论了通过在重要作物中使用高通量实验新定位的候选抗性基因,并将这些潜在的基因靶点分类到防御过程的不同阶段,这将拓宽我们对数量抗该菌性潜在遗传结构的理解。我们提出需要更强大的作图群体来准确可靠地鉴定QDR基因。