<HashMap><database>ENA</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/DRR120/DRR120518/DRR120518_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/DRR120/DRR120518/DRR120518_2.fastq.gz</Fastqsanger.gz></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><center_name>Laboratory for Intestinal Ecosystem, Center for Integrative Medical Sciences, RIKEN</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJDB6618</full_dataset_link><scientific_name>Erysipelotrichaceae bacterium OTU0002</scientific_name><long_description>Accumulating evidence indicates that gut microbes play a pathogenic role in autoimmune diseases including multiple sclerosis (MS). Here, we show that two distinct signals from gut microbes coordinately activate myelin oligodendrocyte glycoprotein (MOG)-specific autoreactive T cells in the small intestine (SI). After induction of experimental autoimmune encephalomyelitis (EAE), an animal model for MS, MOG-specific CD4 T cells can be observed in the SI. Germ-free (GF) mice monocolonized with SI microbes demonstrated that a newly isolated Erysipelotrichaceae strain adheres to SI epithelial cells and enhances Th17 responses, via inducing serum amyloid A and IL-23, that were associated with an increased susceptibility to EAE. Shotgun sequencing of SI contents revealed that a Lactobacillus strain possesses potential mimicry peptides to MOG. While monocolonization of GF mice with the Lactobacillus strain did not enhance EAE development or severity, co-colonized mice with Erysipelotrichaceae and Lactobacillus strains resulted in more severe EAE.</long_description><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>Erysipelotrichaceae bacterium OTU0002</name><description>Erysipelotrichaceae bacterium OTU0002 isolated from mouse small intestine</description><dates><last_updated>2023-05-19</last_updated><first_public>2019-12-21</first_public></dates><accession>PRJDB6618</accession><cross_references><taxon>2066131</taxon></cross_references></HashMap>