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支原体物种的半乳糖脑苷脂生物合成途径:一种引发吉兰-巴雷-施托综合征的抗原。

Galactocerebroside biosynthesis pathways of Mycoplasma species: an antigen triggering Guillain-Barré-Stohl syndrome.

作者信息

Gaspari Erika, Koehorst Jasper J, Frey Joachim, Martins Dos Santos Vitor A P, Suarez-Diez Maria

机构信息

Laboratory of Systems and Synthetic Biology, Wageningen University & Research, Wageningen, the Netherlands.

Vetsuisse, University of Bern, Bern, Switzerland.

出版信息

Microb Biotechnol. 2021 May;14(3):1201-1211. doi: 10.1111/1751-7915.13794. Epub 2021 Mar 27.

Abstract

Infection by Mycoplasma pneumoniae has been identified as a preceding factor of Guillain-Barré-Stohl syndrome. The Guillain-Barré-Stohl syndrome is triggered by an immune reaction against the major glycolipids and it has been postulated that M. pneumoniae infection triggers this syndrome due to bacterial production of galactocerebroside. Here, we present an extensive comparison of 224 genome sequences from 104 Mycoplasma species to characterize the genetic determinants of galactocerebroside biosynthesis. Hidden Markov models were used to analyse glycosil transferases, leading to identification of a functional protein domain, termed M2000535 that appears in about a third of the studied genomes. This domain appears to be associated with a potential UDP-glucose epimerase, which converts UDP-glucose into UDP-galactose, a main substrate for the biosynthesis of galactocerebroside. These findings clarify the pathogenic mechanisms underlining the triggering of Guillain-Barré-Stohl syndrome by M. pneumoniae infections.

摘要

肺炎支原体感染已被确定为吉兰 - 巴雷 - 施托综合征的一个前期因素。吉兰 - 巴雷 - 施托综合征由针对主要糖脂的免疫反应引发,据推测,肺炎支原体感染引发该综合征是由于细菌产生半乳糖脑苷脂。在此,我们对来自104种支原体的224个基因组序列进行了广泛比较,以表征半乳糖脑苷脂生物合成的遗传决定因素。使用隐马尔可夫模型分析糖基转移酶,从而鉴定出一个功能性蛋白质结构域,称为M2000535,约三分之一的研究基因组中出现该结构域。该结构域似乎与一种潜在的UDP - 葡萄糖表异构酶相关,该酶将UDP - 葡萄糖转化为UDP - 半乳糖,UDP - 半乳糖是半乳糖脑苷脂生物合成的主要底物。这些发现阐明了肺炎支原体感染引发吉兰 - 巴雷 - 施托综合征的致病机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7967/8085918/c81ddabf3ae3/MBT2-14-1201-g005.jpg

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