<HashMap><database>iProX</database><scores/><additional><omics_type>Proteomics</omics_type><submitter>Shenhai Gong</submitter><species>Mus Musculus</species><full_dataset_link>http://www.iprox.org/page/project.html?id=IPX0018788000</full_dataset_link><submitter_email>gsh0526@smu.edu.cn</submitter_email><submitter_affiliation>Southern Medical University</submitter_affiliation><sample_protocol></sample_protocol><repository>iProX</repository><data_protocol></data_protocol></additional><is_claimable>false</is_claimable><name>Intestinal β-galactosidase acts as a regulator of sepsis progression</name><description>This project investigates the role of intestinal β-galactosidase in sepsis using 16S rRNA sequencing, metabolomic, and proteomic analyses. Septic patients showed reduced intestinal β-galactosidase activity associated with depletion of putative β-galactosidase-producing bacteria, including Blautia, Faecalibacterium, and Ruminococcus. Metabolomic profiling identified hesperetin as a key microbiota-associated metabolite, and proteomic analysis identified CDK13 as a critical downstream target regulating NLRP3 inflammasome priming and macrophage pyroptosis. Restoration of intestinal β-galactosidase promoted dietary hesperetin liberation and improved survival in septic mice.</description><dates><publication>Wed Aug 05 00:00:00 GMT+01:00 2026</publication></dates><accession>PXD082250</accession><cross_references><TAXONOMY>10090</TAXONOMY></cross_references></HashMap>