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柑橘致病变种核心基因组多位点序列分型用于流行病学和进化分析。

Core-Genome Multilocus Sequence Typing for Epidemiological and Evolutionary Analyses of Phytopathogenic Xanthomonas citri.

机构信息

Department of Life Sciences, Manchester Metropolitan University, Manchester, United Kingdom.

Department of Biology, University of Oxford, Oxford, United Kingdom.

出版信息

Appl Environ Microbiol. 2023 May 31;89(5):e0210122. doi: 10.1128/aem.02101-22. Epub 2023 Apr 17.

Abstract

Xanthomonas citri subsp. is the cause of bacterial citrus canker, responsible for major economic losses to the citrus industry. X. citri subspecies and pathovars are responsible for diseases in soybean, common bean, mango, pomegranate, and cashew. disease has been tracked using several typing methods, but recent studies using genomic sequencing have been key to understanding the evolutionary relationships within the species, including fundamental differences among subsp. pathotypes. Here, we describe a core-genome multilocus sequence typing (cgMLST) scheme for based on 250 genomes comprising multiple examples of subsp. pathotypes A, A*, and A; subsp. ; pv. , pv. , pv. , pv. , pv. , and pv. ; and single isolates of pv. and pv. . This data set included genomic sequencing of 100 novel subsp. isolates. cgMLST, based on 1,618 core genes across 250 genomes, is implemented at PubMLST (https://pubmlst.org/organisms/xanthomonas-citri/). GrapeTree minimum-spanning tree and Interactive Tree of Life (iTOL) neighbor-joining phylogenies generated from the cgMLST data resolved almost identical groupings of isolates to a core-genome single nucleotide polymorphism (SNP)-based neighbor-joining phylogeny. These resolved identical groupings of subsp. pathotypes and subspecies and pathovars. cgMLST should prove to be an increasingly valuable resource for the study of this key species of plant-pathogenic bacteria. Users can submit genomic data and associated metadata for comparison with previously characterized isolates at PubMLST to allow the rapid characterization of the local, national, and global epidemiology of these pathogens and examine evolutionary relationships. Xanthomonas citri is a plant pathogen that causes major economic losses to the citrus industry and sweet orange production in particular. Several subspecies and pathogens are recognized, with host ranges including soybean, common bean, mango, pomegranate, and cashew, among others. Recent genomic studies have shown that host-adapted subspecies and pathovars and subsp. pathotypes form distinct clades. In this study, we describe a core-genome multilocus sequence typing (cgMLST) scheme for this species that can rapidly and robustly discriminate among these ecologically distinct, host-adapted clades. We have established this scheme and associated databases containing genomic sequences and metadata at PubMLST, which users can interrogate with their own genome sequences to determine subspecies, pathovars, and pathotypes. cgMLST should prove to be an invaluable tool for the study of the epidemiology and evolution of this major plant pathogen.

摘要

桔亚属黄单胞菌是细菌性柑橘溃疡病的病原体,是柑橘产业的主要经济损失原因。桔亚属及其致病变种可引起大豆、菜豆、芒果、石榴和腰果等作物的疾病。该病原体已经使用多种分型方法进行了追踪,但最近使用基因组测序的研究对于了解该物种内的进化关系至关重要,包括亚种间的基本差异。亚属的不同路径类型。在这里,我们描述了一个基于 250 个基因组的核心基因组多位点序列分型(cgMLST)方案,其中包括多个桔亚属 A、A*和 A 路径型的例子;桔亚属;pv. 、 pv. 、 pv. 、 pv. 、 pv. 、 pv. ;和 pv. 和 pv. 的单个分离株。该数据集包括 100 个新的桔亚属分离株的基因组测序。cgMLST 基于 250 个基因组中的 1618 个核心基因,在 PubMLST 上实施(https://pubmlst.org/organisms/xanthomonas-citri/)。基于核心基因组单核苷酸多态性(SNP)的邻接法系统发育树和交互式生命树(iTOL)邻接法系统发育树从 cgMLST 数据生成,几乎与基于核心基因组单核苷酸多态性(SNP)的邻接法系统发育树一样,将分离株的分组解析为最小生成树。这些解析与基于核心基因组 SNP 的邻接法系统发育树一样,将桔亚属路径型和亚种的分组解析为相同的分组。cgMLST 应该成为研究这种关键植物病原细菌的越来越有价值的资源。用户可以提交基因组数据和相关元数据,以便与以前表征的分离株在 PubMLST 上进行比较,从而快速表征这些病原体的本地、国家和全球流行病学,并研究进化关系。桔亚属黄单胞菌是一种植物病原体,可导致柑橘产业和甜橙生产遭受重大经济损失。已识别出几个亚种和病原体,其宿主范围包括大豆、菜豆、芒果、石榴和腰果等。最近的基因组研究表明,适应宿主的亚种和致病变种以及桔亚属的路径型形成了不同的进化枝。在这项研究中,我们描述了该物种的核心基因组多位点序列分型(cgMLST)方案,该方案可快速而稳健地区分这些具有生态差异的、适应宿主的进化枝。我们已经在 PubMLST 上建立了这个方案和包含基因组序列和元数据的相关数据库,用户可以使用他们自己的基因组序列来查询这些数据库,以确定亚种、致病变种和路径型。cgMLST 应该成为研究这种主要植物病原体的流行病学和进化的宝贵工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3b1/10231234/c15eff32376d/aem.02101-22-f001.jpg

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