多发性硬化
流动遗传元素
遗传学
生物
计算生物学
细胞生物学
神经科学
基因
免疫学
基因组
作者
Daiki Takewaki,Yuya Kiguchi,Hiroaki Masuoka,Mallahalli S. Manu,Ben J. E. Raveney,Seiko Narushima,Rina Kurokawa,Yusuke Ogata,Yukio Kimura,Noriko Sato,Yusuke Ozawa,Sosuke Yagishita,Toshiyuki Araki,Sachiko Miyake,Wakiro Sato,Wataru Suda,Takashi Yamamura
出处
期刊:Cell Reports
[Elsevier]
日期:2024-09-01
卷期号:: 114785-114785
标识
DOI:10.1016/j.celrep.2024.114785
摘要
Multiple sclerosis (MS) is an autoimmune-demyelinating disease with an inflammatory pathology formed by self-reactive lymphocytes with activated glial cells. Progressive MS, characterized by resistance to medications, significantly differs from the non-progressive form in gut microbiome profiles. After confirming an increased abundance of "Tyzzerella nexilis" in various cohorts of progressive MS, we identified a distinct cluster of T. nexilis strains enriched in progressive MS based on long-read metagenomics. The distinct T. nexilis cluster is characterized by a large number of mobile genetic elements (MGEs) and a lack of defense systems against MGEs. Microbial genes for sulfate reduction and flagella formation with pathogenic implications are specific to this cluster. Moreover, these flagellar genes are encoded on MGEs. Mono-colonization with MGE-enriched T. nexilis made germ-free mice more susceptible to experimental autoimmune encephalomyelitis. These results indicate that the progression of MS may be promoted by MGE-enriched T. nexilis with potentially pathogenic properties.
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