基于比较基因组学的玉米白斑病叶片泛菌菌株的研究

IF 3.7 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Applied and Environmental Microbiology Pub Date : 2025-06-18 Epub Date: 2025-05-19 DOI:10.1128/aem.00329-25
Fenghuan Yang, Miao Li, Hanxiang Wu, Chao Yu, Wende Liu, Huamin Chen
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引用次数: 0

摘要

Pantoea ananatis是肠杆菌科的一员,以其广泛的宿主适应性而闻名。本研究从云南玉米白斑病(MWS)叶片中分离到10株ananatis菌株,并对其功能、基因组多样性和变异进行了分析。接种试验表明,10个分离株均未引起玉米MWS症状。除S47外,9株玉米分离株在烟草中引起过敏反应(hypersensitive response, HR),在洋葱中引起腐烂症状。大多数分离株表现出促进植株生长的特性,其中菌株JCC14、JCY1和S47显著提高了玉米幼苗的生长参数。10个玉米分离株和2个水稻分离株的基因组测序结果显示,12个分离株聚集在3个群体中,并鉴定出一个开放的泛基因组。祖先重建结果表明,A群的基因组大小先增大后减小,在A群和B群的最近共同祖先(MRCA)节点14和7株玉米分离株和其他B群菌株的MRCA节点19上,同源群的基因组大小显著增加。另外,11个单拷贝同源组进行阳性选择。此外,HIVir(高毒力,也称为PASVIL, ananatis特异性毒力位点)集群和VI型分泌系统相关基因在某些ananatis菌株中保守,但与它们的群体差异无关。本研究不仅揭示了mws病玉米褐斑单胞菌分离株的不同功能,而且加深了我们对褐斑单胞菌不同种基因组进化和环境适应的认识。重要意义ananatis是一种常见于各种农用作物的细菌。玉米白斑病是影响玉米最具破坏性的病害之一,造成重大经济损失。本研究明确了P. ananatis菌株在云南玉米叶片定殖,但不是MWS的致病因子。此外,大部分菌株表现出促进植物生长(PGP)活性,诱导烟草过敏反应(HR)活性,并引起洋葱腐烂症状。值得注意的是,在整个进化过程中的差异分析揭示了这些P. ananatis菌株显著的基因组进化和环境适应。这突出了塑造了P. ananatis基因组的基因交换。这些发现提高了我们对ananatis菌株在不同宿主中的功能多样性及其在ananatis物种进化谱系中的位置的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative genomics-based insights into Pantoea ananatis strains, isolated from white spot diseased leaves of maize with plant growth-promoting attributes.

Pantoea ananatis is a member of the Enterobacteriaceae family known for its broad host adaptability. This study isolated 10 P. ananatis strains from white spot (MWS)-diseased leaves of maize (Zea mays) grown in Yunnan Province, China, and analyzed their putative functions, genomic diversity, and variation. The inoculation tests revealed that none of the 10 isolates caused MWS symptoms in maize. Nine maize isolates, except for S47, induced a hypersensitive response (HR) in tobacco and caused rot symptoms in onion. Most isolates exhibited plant growth-promoting characteristics, with strains JCC14, JCY1, and S47 significantly enhancing maize seedling growth parameters. Genomic sequencing of 10 maize isolates and two rice isolates revealed that 12 isolates clustered into three groups, with an open pan-genome identified. Ancestral reconstruction indicated that the genome size increased in Group A and then decreased in Group B, with significant gains in orthologous groups at Node 14, the most recent common ancestor (MRCA) of Group A and Group B, and at Node 19, the MRCA of seven maize-isolated strains and other Group B strains. Additionally, 11 single-copy orthologous groups were under positive selection. Furthermore, the HIVir (high virulence, also known as PASVIL, P. ananatis-specific virulence locus) cluster and type VI secretion system-related genes were conserved in certain P. ananatis strains but were not related to their group divergences. This study not only reveals the diverse functions of MWS-diseased maize P. ananatis isolates, but also enhances our understanding of divergent genome evolution and environmental adaptation across P. ananatis species.IMPORTANCEPantoea ananatis is a bacterium commonly found in various agronomic crops. Maize white spot (MWS) has been one of the most destructive diseases affecting maize, leading to significant economic losses. This study clarified that P. ananatis strains colonized maize leaves but were not the causal agents of MWS in Yunnan Province, China. Moreover, most of these P. ananatis strains exhibited plant growth-promoting (PGP) activities, induced hypersensitive response (HR) activity on tobacco, and caused rot symptoms in onion. Notably, the analysis of divergence throughout the evolutionary process revealed significant genomic evolution and environmental adaptation in these P. ananatis strains. This highlights the genetic exchange that has shaped the genome of P. ananatis. These findings improve our understanding of the functional diversity of P. ananatis strains across different hosts and their positions within the evolutionary lineages of P. ananatis species.

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来源期刊
Applied and Environmental Microbiology
Applied and Environmental Microbiology 生物-生物工程与应用微生物
CiteScore
7.70
自引率
2.30%
发文量
730
审稿时长
1.9 months
期刊介绍: Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.
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