Dynamic mini-chromosomes: mechanisms of exchange, stability and causation of fungal pathogen adaptation
Dynamic mini-chromosomes: mechanisms of exchange, stability and causation of fungal pathogen adaptation
批准号:
2011500
负责人:
Sanzhen Liu
金额:
$60.0万
依托单位:
依托单位国家:
美国
项目类别:
Continuing Grant
财政年份:
2021
资助国家:
美国
项目状态:
未结题
起止时间:
2021-07-01 至 2025-06-30
中文摘要
粮食作物不断受到既有病原体的新变种和新出现的病原体的威胁。稻瘟病真菌Magnaporthe oryzae有很长的变异历史,以克服水稻作物中的抗性,1985年出现了一种新的M. oryzae变体,对巴西的小麦造成了毁灭性的疾病。小麦稻瘟病被证明比水稻稻瘟病更难控制,因为利用20世纪80年代的菌株鉴定出的潜在抗性基因不再有效地控制最近的侵袭性分离株。该疾病的全球传播和缺乏控制措施加剧了人们对全球粮食安全的担忧。最近的研究表明,从爆炸场分离物中分离出的多余染色体可能加速了真菌的适应性进化,并有助于增强其毒力。据推测,多余染色体在病原菌基因的进化中发挥着重要作用,这些基因对寄主植物的抗性至关重要,包括寄主在植物种/属和作物品种水平上的特异性。该项目将研究多余染色体,以了解它们的流行、菌株之间的移动、与核心染色体的DNA交换、稳定性以及对致病性和毒力的贡献。结果将有助于理解爆炸病原体的基因组动力学,并有助于揭示多余染色体在许多植物、动物和其他真菌中的作用。研究生和本科生将接受基因组学、生物信息学、分子植物-微生物相互作用和植物生物安全方面的广泛培训。本科生将参加为期8周的夏季植物疾病诊断研究经验,包括在野外收集和使用尖端测序技术鉴定疾病生物体。稻瘟病菌在50多种禾草上引起稻瘟病,其中包括古老的水稻稻瘟病和新出现的小麦稻瘟病。由爆炸病和进化的病原体构成的全球农业威胁使得了解爆炸病原体的基因组动力学变得重要。爆炸真菌基因组包括数百个假定的效应基因,这些基因在宿主入侵期间特异性表达,通常编码促进疾病的小分泌蛋白。这些效应物的一个子集被宿主抗性基因产物识别,从而触发抗性并阻止宿主的感染。在宿主种/属水平和作物品种水平上,这些效应物在确定宿主对瘟病真菌病原体的特异性方面发挥着重要作用。最近对小麦稻瘟病地分离物的基因组数据表明,这些多余染色体中含有许多在其他菌株中经常发现的核心染色体上的效应基因,以及其他可能在病原体侵袭性中起作用的基因。本项目旨在进一步了解多余染色体的流行、菌株间运动、与核心染色体的DNA交换、稳定性以及对致病性和毒力的贡献。多余染色体作为从核心染色体上删除的效应基因的储存库,并在介导其在核心染色体上的重新定位中发挥作用,从而在效应迁移中发挥作用,这一假设将得到验证。该项目将结合blast疾病生物学的方法,包括适应性进化策略、真菌菌株之间的拟性转移、分子生物学、基因组学和细胞学。该奖项反映了美国国家科学基金会的法定使命,并通过使用基金会的知识价值和更广泛的影响审查标准进行评估,被认为值得支持。
英文摘要
Food crops are constantly threatened by new variants of established pathogens and by newly-emerged pathogens. The rice blast fungus Magnaporthe oryzae has a long history of variation to overcome resistance deployed in rice crops, and a new M. oryzae variant emerged in 1985 to cause devastating disease on wheat in Brazil. Wheat blast disease is proving even harder to control than rice blast because potential resistance genes identified using strains from the 1980s are no longer effective in controlling recent aggressive isolates. Global spread of the disease and lack of control measures enhance fears about global food security. Recent studies indicated that dispensable supernumerary chromosomes from blast field isolates might accelerate adaptive evolution and contribute to virulence of the fungus. Supernumerary chromosomes are hypothesized to play roles in the evolution of pathogen genes that are critical for resistance in host plants, including host specificity at the plant species/genus and the crop cultivar levels. The project will study supernumerary chromosomes to understand their prevalence, movement between strains, DNA exchange with core-chromosomes, stability, and contributions to pathogenicity and virulence. Outcomes will be valuable for understanding genomic dynamics of the blast pathogen and help reveal roles of supernumerary chromosomes in many plants, animals and other fungi. Graduate students and undergraduates will receive broad training in genomics, bioinformatics, molecular plant-microbe interactions, and plant biosecurity. Undergraduates will participate in an 8-week summer research experience in plant disease diagnostics involving collections in the field and identification of disease organisms using cutting edge sequencing technologies. The fungus Magnaporthe oryzae causes blast diseases on more than 50 grass species, which include the ancient rice blast and the newly emerged wheat blast. Global agricultural threats posed by blast diseases and evolving pathogens make it important to understand genome dynamics of blast pathogens. The blast fungal genome includes hundreds of putative effector genes that are specifically expressed during host invasion and that generally encode small secreted proteins involved promoting disease. A subset of these effectors is recognized by host resistance gene products, which triggers resistance and blocks infection of that host. Such effectors play a major role in determining host specificity in blast fungal pathogens, both at the host species/genus level, and at the crop cultivar level. The recent genomic data of dispensable supernumerary chromosomes from the wheat blast field isolates showed that the supernumerary chromosomes contain many effector genes that are often found on indispensable core-chromosomes in other strains, as well as other genes that may play a role in pathogen aggressiveness. This project proposes to further understand supernumerary chromosomes with respect to their prevalence, inter-strain movement, DNA exchange with core-chromosomes, stability, and contributions to pathogenicity and virulence. The hypothesis will be tested that supernumerary chromosomes play roles in effector mobility by serving as a repository for effector genes that are deleted from core-chromosomes, and a role in mediating their relocation on core-chromosomes. The project will combine methodologies in blast disease biology, including adaptive evolution strategies, parasexual transfer between fungal strains, molecular biology, genomics, and cytology.This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.
期刊论文(5)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1016/j.pmpp.2023.102006
发表时间:
2023-03
期刊:
Physiological and Molecular Plant Pathology
影响因子:
2.7
作者:
[Jun Huang;Sanzhen Liu;D. Cook]
通讯作者:
Jun Huang;Sanzhen Liu;D. Cook
Collaborative Research: RESEARCH-PGR: PlantTransform: The Genetic Basis of Maize Regeneration and Applications to Plant Transformation
-
批准号:2311738
-
项目类别:Standard Grant
-
资助金额:$192.07万
-
财政年份:2023
-
负责人:Sanzhen Liu
-
依托单位:
ECA-PGR: Under the Hood: The Genetic Components of Maize Transformation
-
批准号:1741090
-
项目类别:Continuing Grant
-
资助金额:$239.86万
-
财政年份:2018
-
负责人:Sanzhen Liu
-
依托单位:
Collaborative Research: The role of host nutrient carriers in pathogen susceptibility
-
批准号:1258028
-
项目类别:Standard Grant
-
资助金额:$37.49万
-
财政年份:2013
-
负责人:Sanzhen Liu
-
依托单位:
国内基金
海外基金
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