Identification of trypsin-degrading commensals in the large intestine

Article

关键词: O-GLYCOSYLATION SYSTEM;    TRYPTIC ACTIVITY;    PANCREATIC ENDOPEPTIDASES;    GUT MICROBIOME;    HUMAN COLON;    POLYSACCHARIDE;    INACTIVATION;    ACTIVATION;    INDUCTION;    SECRETION;   

DOI  :  10.1038/s41586-022-05181-3

来源: SCIE

【 摘 要 】

Increased levels of proteases, such as trypsin, in the distal intestine have been implicated in intestinal pathological conditions(1-3). However, the players and mechanisms that underlie protease regulation in the intestinal lumen have remained unclear. Here we show that Paraprevotella strains isolated from the faecal microbiome of healthy human donors are potent trypsin-degrading commensals. Mechanistically, Paraprevotella recruit trypsin to the bacterial surface through type IX secretion system-dependent polysaccharide-anchoring proteins to promote trypsin autolysis. Paraprevotella colonization protects IgA from trypsin degradation and enhances the effectiveness of oral vaccines against Citrobacter rodentium. Moreover, Paraprevotella colonization inhibits lethal infection with murine hepatitis virus-2, a mouse coronavirus that is dependent on trypsin and trypsin-like proteases for entry into host cells(4,5). Consistently, carriage of putative genes involved in trypsin degradation in the gut microbiome was associated with reduced severity of diarrhoea in patients with SARS-CoV-2 infection. Thus, trypsin-degrading commensal colonization may contribute to the maintenance of intestinal homeostasis and protection from pathogen infection.

【 授权许可】

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