首页> 外文期刊>Molecular Plant-Microbe Interactions >Genome Sequencing and Transposon Mutagenesis of Burkholderia seminalis TC3.4.2R3 Identify Genes Contributing to Suppression of Orchid Necrosis Caused by B-gladioli
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Genome Sequencing and Transposon Mutagenesis of Burkholderia seminalis TC3.4.2R3 Identify Genes Contributing to Suppression of Orchid Necrosis Caused by B-gladioli

机译:伯克霍尔德氏菌TC3.4.2R3的基因组测序和转座子诱变鉴定了有助于抑制B-唐diol蒲引起的兰花坏死的基因。

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摘要

From a screen of 36 plant-associated strains of Burkholderia spp., we identified 24 strains that suppressed leaf and pseudobulb necrosis of orchid caused by B. gladioli. To gain insights into the mechanisms of disease suppression, we generated a draft genome sequence from one suppressive strain, TC3.4.2R3. The genome is an estimated 7.67 megabases in size, with three replicons, two chromosomes, and the plasmid pC3. Using a combination of multilocus sequence analysis and phylogenomics, we identified TC3.4.2R3 as B. seminalis, a species within the Burkholderia cepacia complex that includes opportunistic human pathogens and environmental strains. We generated and screened a library of 3,840 transposon mutants of strain TC3.4.2R3 on orchid leaves to identify genes contributing to plant disease suppression. Twelve mutants deficient in suppression of leaf necrosis were selected and the transposon insertions were mapped to eight loci. One gene is in a wcb cluster that is related to synthesis of extracellular polysaccharide, a key determinant in bacterial-host interactions in other systems, and the other seven are highly conserved among Burkholderia spp. The fundamental information developed in this study will serve as a resource for future research aiming to identify mechanisms contributing to biological control.
机译:从36个与植物相关的Burkholderia spp。菌株的筛选中,我们鉴定了24个抑制了剑兰(B.gladioli)引起的兰花的叶片和假鳞茎坏死的菌株。为了深入了解疾病抑制的机制,我们从一种抑制株TC3.4.2R3生成了一份基因组序列草案。基因组的大小估计为7.67兆碱基,具有三个复制子,两个染色体和质粒pC3。使用多基因座序列分析和系统发育组学的组合,我们将TC3.4.2R3鉴定为B. seminalis,这是洋葱伯克霍尔德菌中的一种,其中包括机会性人类病原体和环境菌株。我们在兰花叶片上产生并筛选了菌株TC3.4.2R3的3840个转座子突变体的文库,以鉴定有助于抑制植物病害的基因。选择缺乏抑制叶片坏死的十二个突变体,并将转座子插入定位到八个位点。一个基因在wcb簇中,与胞外多糖的合成有关,胞外多糖是其他系统中细菌与宿主相互作用的关键决定因素,而其他七个在伯克霍尔德氏菌中高度保守。本研究中开发的基本信息将作为未来研究的资源,旨在确定有助于生物控制的机制。

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