Nathaniel J. Winsor, Giuliano Bayer, Ojas Singh, Jeremy K. Chan, Lu Yi Li, Brandon Y. Lieng, Elisabeth Foerster, Ana Popovic, Boyan K. Tsankov, Heather Maughan, Paul Lemire, Elaine Tam, Catherine Streutker, Lina Chen, Stacey L. Heaver, Ruth E. Ley, John Parkinson, J. Rafael Montenegro-Burke, George M.H. Birchenough, Dana J. Philpott, Stephen E. Girardin
{"title":"通过 NLRP6 跨领域检测肠道原生动物","authors":"Nathaniel J. Winsor, Giuliano Bayer, Ojas Singh, Jeremy K. Chan, Lu Yi Li, Brandon Y. Lieng, Elisabeth Foerster, Ana Popovic, Boyan K. Tsankov, Heather Maughan, Paul Lemire, Elaine Tam, Catherine Streutker, Lina Chen, Stacey L. Heaver, Ruth E. Ley, John Parkinson, J. Rafael Montenegro-Burke, George M.H. Birchenough, Dana J. Philpott, Stephen E. Girardin","doi":"10.1016/j.chom.2025.02.008","DOIUrl":null,"url":null,"abstract":"Intestinal protists are detected by the host innate immune system through mechanisms that remain poorly understood. Here, we demonstrate that <em>Tritrichomonas</em> protozoa induce thickening of the colonic mucus in an NLRP6-, ASC-, and caspase-11-dependent manner, consistent with the activation of sentinel goblet cells. Mucus growth is recapitulated with cecal extracts from <em>Tritrichomonas</em>-infected mice but not purified protozoa, suggesting that NLRP6 may detect infection-induced microbial dysbiosis. In agreement, <em>Tritrichomonas</em> infection causes a shift in the microbiota with the expansion of <em>Bacteroides</em> and <em>Prevotella</em>, and untargeted metabolomics reveals a dramatic increase in several classes of metabolites, including sphingolipids. Finally, using a combination of gnotobiotic mice and <em>ex vivo</em> mucus analysis, we demonstrate that wild-type, but not sphingolipid-deficient, <em>B. thetaiotaomicron</em> is sufficient to induce NLRP6-dependent sentinel goblet cell function, with the greatest effect observed in female mice. Thus, we propose that NLRP6 is a sensor of intestinal protozoa infection through monitoring microbial sphingolipids.","PeriodicalId":9693,"journal":{"name":"Cell host & microbe","volume":"29 1","pages":""},"PeriodicalIF":20.6000,"publicationDate":"2025-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Cross-kingdom-mediated detection of intestinal protozoa through NLRP6\",\"authors\":\"Nathaniel J. Winsor, Giuliano Bayer, Ojas Singh, Jeremy K. Chan, Lu Yi Li, Brandon Y. Lieng, Elisabeth Foerster, Ana Popovic, Boyan K. Tsankov, Heather Maughan, Paul Lemire, Elaine Tam, Catherine Streutker, Lina Chen, Stacey L. Heaver, Ruth E. Ley, John Parkinson, J. Rafael Montenegro-Burke, George M.H. Birchenough, Dana J. Philpott, Stephen E. Girardin\",\"doi\":\"10.1016/j.chom.2025.02.008\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Intestinal protists are detected by the host innate immune system through mechanisms that remain poorly understood. Here, we demonstrate that <em>Tritrichomonas</em> protozoa induce thickening of the colonic mucus in an NLRP6-, ASC-, and caspase-11-dependent manner, consistent with the activation of sentinel goblet cells. Mucus growth is recapitulated with cecal extracts from <em>Tritrichomonas</em>-infected mice but not purified protozoa, suggesting that NLRP6 may detect infection-induced microbial dysbiosis. In agreement, <em>Tritrichomonas</em> infection causes a shift in the microbiota with the expansion of <em>Bacteroides</em> and <em>Prevotella</em>, and untargeted metabolomics reveals a dramatic increase in several classes of metabolites, including sphingolipids. Finally, using a combination of gnotobiotic mice and <em>ex vivo</em> mucus analysis, we demonstrate that wild-type, but not sphingolipid-deficient, <em>B. thetaiotaomicron</em> is sufficient to induce NLRP6-dependent sentinel goblet cell function, with the greatest effect observed in female mice. Thus, we propose that NLRP6 is a sensor of intestinal protozoa infection through monitoring microbial sphingolipids.\",\"PeriodicalId\":9693,\"journal\":{\"name\":\"Cell host & microbe\",\"volume\":\"29 1\",\"pages\":\"\"},\"PeriodicalIF\":20.6000,\"publicationDate\":\"2025-03-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cell host & microbe\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1016/j.chom.2025.02.008\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell host & microbe","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.chom.2025.02.008","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
Cross-kingdom-mediated detection of intestinal protozoa through NLRP6
Intestinal protists are detected by the host innate immune system through mechanisms that remain poorly understood. Here, we demonstrate that Tritrichomonas protozoa induce thickening of the colonic mucus in an NLRP6-, ASC-, and caspase-11-dependent manner, consistent with the activation of sentinel goblet cells. Mucus growth is recapitulated with cecal extracts from Tritrichomonas-infected mice but not purified protozoa, suggesting that NLRP6 may detect infection-induced microbial dysbiosis. In agreement, Tritrichomonas infection causes a shift in the microbiota with the expansion of Bacteroides and Prevotella, and untargeted metabolomics reveals a dramatic increase in several classes of metabolites, including sphingolipids. Finally, using a combination of gnotobiotic mice and ex vivo mucus analysis, we demonstrate that wild-type, but not sphingolipid-deficient, B. thetaiotaomicron is sufficient to induce NLRP6-dependent sentinel goblet cell function, with the greatest effect observed in female mice. Thus, we propose that NLRP6 is a sensor of intestinal protozoa infection through monitoring microbial sphingolipids.
期刊介绍:
Cell Host & Microbe is a scientific journal that was launched in March 2007. The journal aims to provide a platform for scientists to exchange ideas and concepts related to the study of microbes and their interaction with host organisms at a molecular, cellular, and immune level. It publishes novel findings on a wide range of microorganisms including bacteria, fungi, parasites, and viruses. The journal focuses on the interface between the microbe and its host, whether the host is a vertebrate, invertebrate, or plant, and whether the microbe is pathogenic, non-pathogenic, or commensal. The integrated study of microbes and their interactions with each other, their host, and the cellular environment they inhabit is a unifying theme of the journal. The published work in Cell Host & Microbe is expected to be of exceptional significance within its field and also of interest to researchers in other areas. In addition to primary research articles, the journal features expert analysis, commentary, and reviews on current topics of interest in the field.