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番茄木质部汁液中三种植物病原物种适合度因子的全基因组鉴定

Genome-Wide Identification of Tomato Xylem Sap Fitness Factors for Three Plant-Pathogenic Species.

作者信息

Georgoulis Stratton J, Shalvarjian Katie E, Helmann Tyler C, Hamilton Corri D, Carlson Hans K, Deutschbauer Adam M, Lowe-Power Tiffany M

机构信息

Department of Plant Pathology, University of California Davis, Davis, California, USA.

Department of Plant and Microbial Biology, University of California Berkeley, Berkeley, California, USA.

出版信息

mSystems. 2021 Dec 21;6(6):e0122921. doi: 10.1128/mSystems.01229-21. Epub 2021 Nov 2.

Abstract

Plant-pathogenic spp. colonize plant xylem and cause wilt diseases on a broad range of host plants. To identify genes that promote growth of diverse strains in xylem sap from tomato plants, we performed genome-scale genetic screens (random barcoded transposon mutant sequencing screens [RB-TnSeq]) in three strains spanning the genetic, geographical, and physiological range of plant-pathogenic : Ralstonia solanacearum IBSBF1503, Ralstonia pseudosolanacearum GMI1000, and Ralstonia syzygii PSI07. Contrasting mutant fitness phenotypes in culture media versus in xylem sap suggest that strains are adapted to xylem sap and that culture media impose foreign selective pressures. Although wild-type grew in sap and in rich medium with similar doubling times and to a similar carrying capacity, more genes were essential for growth in sap than in rich medium. Each strain required many genes associated with envelope remodeling and repair processes for full fitness in xylem sap. These genes were associated with peptidoglycan peptide formation (), secretion of periplasmic proteins (), periplasmic protein folding (), synthesis of osmoregulated periplasmic glucans (), and lipopolysaccharide (LPS) biosynthesis. Mutant strains with mutations in four genes had strong, sap-specific fitness defects in all strain backgrounds: , , , and a lipoprotein (RSc2007). Many amino acid biosynthesis genes were required for fitness in both minimal medium and xylem sap. Multiple mutants with insertions in virulence regulators had gains of fitness in culture media and neutral fitness in sap. Our genome-scale genetic screen identified fitness factors that promote growth in xylem sap, an ecologically relevant condition. Traditional transposon mutagenesis genetic screens pioneered molecular plant pathology and identified core virulence traits like the type III secretion system. TnSeq approaches that leverage next-generation sequencing to rapidly quantify transposon mutant phenotypes are ushering in a new wave of biological discovery. Here, we have adapted a genome-scale approach, random barcoded transposon mutant sequencing (RB-TnSeq), to discover fitness factors that promote growth of three related bacterial strains in a common niche, tomato xylem sap. Fitness of the wild type and mutants show that spp. are adapted to grow well in xylem sap from their natural host plant, tomato. Our screen identified multiple sap-specific fitness factors with roles in maintaining the bacterial envelope. These factors include putative adaptations to resist plant defenses that may include antimicrobial proteins and specialized metabolites that damage bacterial membranes.

摘要

植物致病定殖于植物木质部,可在多种寄主植物上引发枯萎病。为了鉴定促进不同菌株在番茄植物木质部汁液中生长的基因,我们在跨越植物致病的遗传、地理和生理范围的三个菌株中进行了全基因组规模的遗传筛选(随机条形码转座子突变体测序筛选 [RB-TnSeq]):青枯雷尔氏菌IBSBF1503、假青枯雷尔氏菌GMI1000和番荔枝雷尔氏菌PSI07。在培养基与木质部汁液中突变体适应性表型的对比表明,菌株适应木质部汁液,而培养基施加了外来的选择压力。尽管野生型菌株在汁液和丰富培养基中生长时具有相似的倍增时间和相似的承载能力,但在汁液中生长所需的基因比在丰富培养基中更多。每个菌株在木质部汁液中实现完全适应性都需要许多与包膜重塑和修复过程相关的基因。这些基因与肽聚糖肽的形成()、周质蛋白的分泌()、周质蛋白折叠()、渗透调节周质葡聚糖的合成()以及脂多糖(LPS)生物合成有关。在四个基因中发生突变的突变菌株在所有菌株背景下都具有强烈的、汁液特异性的适应性缺陷:、、和一种脂蛋白(RSc2007)。在基本培养基和木质部汁液中生长都需要许多氨基酸生物合成基因。在毒力调节因子中插入的多个突变体在培养基中适应性增强,在汁液中适应性中性。我们的全基因组规模遗传筛选鉴定出了促进在木质部汁液(一种生态相关条件)中生长的适应性因子。传统的转座子诱变遗传筛选开创了分子植物病理学,并鉴定出了核心毒力性状,如III型分泌系统。利用下一代测序快速量化转座子突变体表型的TnSeq方法正在引领新一轮的生物学发现。在这里,我们采用了一种全基因组规模的方法,即随机条形码转座子突变体测序(RB-TnSeq),来发现促进三种相关细菌菌株在共同生态位——番茄木质部汁液中生长的适应性因子。野生型和突变体的适应性表明,适应于在其自然寄主植物番茄的木质部汁液中良好生长。我们的筛选鉴定出了多个在维持细菌包膜方面起作用的汁液特异性适应性因子。这些因子包括可能对抵抗植物防御的推定适应性,植物防御可能包括抗菌蛋白和破坏细菌膜的特殊代谢产物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8470/8562481/6426cfb8e6b5/msystems.01229-21-f001.jpg

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