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Comparative genomic analysis of Campylobacter jejuni associated with Guillain-Barré and Miller Fisher syndromes: neuropathogenic and enteritis-associated isolates can share high levels of genomic similarity

机译:空肠弯曲杆菌与格林-巴利和米勒·费希尔综合症相关的基因组比较分析:神经病原体和肠炎相关菌株可共享高水平的基因组相似性

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摘要

BackgroundCampylobacter jejuni infection represents the most frequent antecedent infection triggering the onset of the neuropathic disorders Guillain-Barré syndrome (GBS) and Miller Fisher syndrome (MFS). Although sialylated ganglioside-mimicking lipo-oligosaccharide (LOS) structures are the strongest neuropathogenic determinants in C. jejuni, they do not appear to be the only requirement for a neuropathic outcome since strains capable of their production have been isolated from patients with uncomplicated cases of enteritis. Consequently, other pathogen and/or host-related factors contribute to the onset of neurological complications. We have used comparative genomic hybridization to perform a detailed genomic comparison of strains isolated from GBS/MFS and enteritis-only patients. Our dataset, in which the gene conservation profile for 1712 genes was assayed in 102 strains, including 56 neuropathogenic isolates, represents the largest systematic search for C. jejuni factors associated with GBS/MFS to date and has allowed us to analyze the genetic background of neuropathogenic C. jejuni strains with an unprecedented level of resolution.
机译:背景空肠弯曲杆菌感染是引发神经性疾病吉兰—巴雷综合征(GBS)和米勒·费雪综合症(MFS)发作的最常见的前期感染。尽管唾液酸化的神经节苷脂模拟脂寡糖(LOS)结构是空肠弯曲杆菌中最强的神经病决定因素,但由于能够从无并发症的病例中分离出能够产生其病原菌的菌株,因此它们似乎并不是神经病理学结果的唯一要求。肠炎。因此,其他病原体和/或宿主相关因素也导致神经系统并发症的发作。我们已经使用比较基因组杂交技术对从GBS / MFS和仅肠炎患者中分离出的菌株进行了详细的基因组比较。我们的数据集在102个菌株中检测了1712个基因的基因保守性,其中包括56个神经致病菌,代表了迄今为止与GBS / MFS相关的空肠弯曲杆菌因子的最大系统搜索,这使我们能够分析空肠弯曲菌的遗传背景。神经病空肠弯曲杆菌菌株具有前所未有的分辨率。

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