Sandra L Arias, Ellen W van Wijngaarden, Diana Balint, Joshua Jones, Carl C Crawford, Parul J Shukla, Meredith Silberstein, Ilana L Brito
{"title":"环境因素驱动细菌降解胃肠道粘液。","authors":"Sandra L Arias, Ellen W van Wijngaarden, Diana Balint, Joshua Jones, Carl C Crawford, Parul J Shukla, Meredith Silberstein, Ilana L Brito","doi":"10.1038/s41522-025-00741-7","DOIUrl":null,"url":null,"abstract":"<p><p>The mucus layer lining the gastrointestinal tract is essential for gut health, providing a protective barrier while maintaining host-microbiome symbiosis. Its disruption is a hallmark of diseases like ulcerative colitis, yet how bacterial activity impacts mucus structure remains unclear. We developed a method to collect human-cell-derived mucus that mimics human colonic mucus and used it to investigate mucus degradation by commensal bacteria. Glycan foraging by species such as Bacteroides thetaiotaomicron and Bacteroides fragilis did not alter mucus rheology. Instead, secreted proteases were the primary drivers of degradation. Protease activity by B. fragilis and Bifidobacterium longum subsp. infantis was nutrient-dependent, while Enterococcus faecalis was further influenced by oxygen. Under oxidative stress, E. faecalis upregulated carbohydrate metabolism and virulence genes. These results reveal that bacterial mucus degradation is context-dependent and shaped by environmental factors. Our findings underscore the value of human cell-derived mucus models for understanding bacteria-mucus interactions in health and disease.</p>","PeriodicalId":19370,"journal":{"name":"npj Biofilms and Microbiomes","volume":"11 1","pages":"133"},"PeriodicalIF":7.8000,"publicationDate":"2025-07-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Environmental factors drive bacterial degradation of gastrointestinal mucus.\",\"authors\":\"Sandra L Arias, Ellen W van Wijngaarden, Diana Balint, Joshua Jones, Carl C Crawford, Parul J Shukla, Meredith Silberstein, Ilana L Brito\",\"doi\":\"10.1038/s41522-025-00741-7\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The mucus layer lining the gastrointestinal tract is essential for gut health, providing a protective barrier while maintaining host-microbiome symbiosis. Its disruption is a hallmark of diseases like ulcerative colitis, yet how bacterial activity impacts mucus structure remains unclear. We developed a method to collect human-cell-derived mucus that mimics human colonic mucus and used it to investigate mucus degradation by commensal bacteria. Glycan foraging by species such as Bacteroides thetaiotaomicron and Bacteroides fragilis did not alter mucus rheology. Instead, secreted proteases were the primary drivers of degradation. Protease activity by B. fragilis and Bifidobacterium longum subsp. infantis was nutrient-dependent, while Enterococcus faecalis was further influenced by oxygen. Under oxidative stress, E. faecalis upregulated carbohydrate metabolism and virulence genes. These results reveal that bacterial mucus degradation is context-dependent and shaped by environmental factors. Our findings underscore the value of human cell-derived mucus models for understanding bacteria-mucus interactions in health and disease.</p>\",\"PeriodicalId\":19370,\"journal\":{\"name\":\"npj Biofilms and Microbiomes\",\"volume\":\"11 1\",\"pages\":\"133\"},\"PeriodicalIF\":7.8000,\"publicationDate\":\"2025-07-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"npj Biofilms and Microbiomes\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1038/s41522-025-00741-7\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOTECHNOLOGY & APPLIED MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"npj Biofilms and Microbiomes","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1038/s41522-025-00741-7","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
Environmental factors drive bacterial degradation of gastrointestinal mucus.
The mucus layer lining the gastrointestinal tract is essential for gut health, providing a protective barrier while maintaining host-microbiome symbiosis. Its disruption is a hallmark of diseases like ulcerative colitis, yet how bacterial activity impacts mucus structure remains unclear. We developed a method to collect human-cell-derived mucus that mimics human colonic mucus and used it to investigate mucus degradation by commensal bacteria. Glycan foraging by species such as Bacteroides thetaiotaomicron and Bacteroides fragilis did not alter mucus rheology. Instead, secreted proteases were the primary drivers of degradation. Protease activity by B. fragilis and Bifidobacterium longum subsp. infantis was nutrient-dependent, while Enterococcus faecalis was further influenced by oxygen. Under oxidative stress, E. faecalis upregulated carbohydrate metabolism and virulence genes. These results reveal that bacterial mucus degradation is context-dependent and shaped by environmental factors. Our findings underscore the value of human cell-derived mucus models for understanding bacteria-mucus interactions in health and disease.
期刊介绍:
npj Biofilms and Microbiomes is a comprehensive platform that promotes research on biofilms and microbiomes across various scientific disciplines. The journal facilitates cross-disciplinary discussions to enhance our understanding of the biology, ecology, and communal functions of biofilms, populations, and communities. It also focuses on applications in the medical, environmental, and engineering domains. The scope of the journal encompasses all aspects of the field, ranging from cell-cell communication and single cell interactions to the microbiomes of humans, animals, plants, and natural and built environments. The journal also welcomes research on the virome, phageome, mycome, and fungome. It publishes both applied science and theoretical work. As an open access and interdisciplinary journal, its primary goal is to publish significant scientific advancements in microbial biofilms and microbiomes. The journal enables discussions that span multiple disciplines and contributes to our understanding of the social behavior of microbial biofilm populations and communities, and their impact on life, human health, and the environment.