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Identification of innate immunity elicitors using molecular signatures of natural selection

机译:利用自然选择的分子特征识别先天免疫引发剂

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The innate immune system is an ancient and broad-spectrum defense system found in all eukaryotes. The detection of microbial elicitors results in the up-regulation of defense-related genes and the elicitation of inflammatory and apoptotic responses. These innate immune responses are the front-line barrier against disease because they collectively suppress the growth of the vast majority of invading microbes. Despite their critical role, we know remarkably little about the diversity of immune elicitors. To address this paucity, we reasoned that hosts are more likely to evolve recognition to "core" pathogen proteins under strong negative selection for the maintenance of essential cellular functions, whereas repeated exposure to host-defense responses will impose strong positive selective pressure for elicitor diversification to avoid host recognition. Therefore, we hypothesized that novel bacterial elicitors can be identified through these opposing forces of natural selection. We tested this hypothesis by examining the genomes of six bacterial phytopathogens and identifying 56 candidate elicitors that have an excess of positively selected residues in a background of strong negative selection. We show that these positively selected residues are atypically clustered, similar to patterns seen in the few well-characterized elicitors. We then validated selected candidate elicitors by showing that they induce Arabidopsis thaliana innate immunity in functional (virulence suppression) and cellular (callose deposition) assays. These finding provide targets for the study of host-pathogen interactions and applied research into alternative antimicrobial treatments.
机译:先天免疫系统是在所有真核生物中发现的古老而广谱的防御系统。微生物激发子的检测导致防御相关基因的上调,并引起炎症和凋亡反应。这些先天免疫反应是抵抗疾病的一线屏障,因为它们共同抑制了绝大多数入侵微生物的生长。尽管它们起着至关重要的作用,但我们对免疫引发剂的多样性知之甚少。为了解决这一问题,我们认为宿主在维持细胞功能必需的强烈阴性选择下更可能进化为“核心”病原体蛋白的识别,而反复暴露于宿主防御反应将对激发子多样化施加强大的正选择压力。避免主机识别。因此,我们假设可以通过这些自然选择的相反作用力来鉴定新型细菌引发剂。我们通过检查六个细菌性植物病原体的基因组并鉴定出56个候选激发子来检验这一假设,这些候选激发子在强烈的负选择背景下具有过量的正选择残基。我们表明,这些积极选择的残基是非典型地聚类,类似于在少数特征明确的激发子中看到的模式。然后,我们通过显示在功能(毒性抑制)和细胞(愈伤组织沉积)测定中诱导拟南芥先天免疫来验证选定的候选激发子。这些发现为研究宿主-病原体之间的相互作用以及将其应用于替代性抗生素治疗提供了目标。

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