Yiyi Liu, Yu-Yu Cheng, Jaron Thompson, Zhichao Zhou, Eugenio I Vivas, Matthew F Warren, Federico E Rey, Karthik Anantharaman, Ophelia S Venturelli
{"title":"精氨酸二水解酶途径影响人类肠道微生物群落的组装、功能和哺乳动物宿主的定植","authors":"Yiyi Liu, Yu-Yu Cheng, Jaron Thompson, Zhichao Zhou, Eugenio I Vivas, Matthew F Warren, Federico E Rey, Karthik Anantharaman, Ophelia S Venturelli","doi":"10.1101/2023.01.10.523442","DOIUrl":null,"url":null,"abstract":"<p><p>The arginine dihydrolase pathway (<i>arc</i> operon) present in a subset of diverse human gut species enables arginine catabolism. This specialized metabolic pathway can alter environmental pH and nitrogen availability, which in turn could shape gut microbiota inter-species interactions. By exploiting synthetic control of gene expression, we investigated the role of the <i>arc</i> operon in probiotic <i>Escherichia coli</i> Nissle 1917 on human gut community assembly and health-relevant metabolite profiles <i>in vitro</i> and in the murine gut. By stabilizing environmental pH, the <i>arc</i> operon reduced variability in community composition across different initial pH perturbations. The abundance of butyrate producing bacteria were altered in response to <i>arc</i> operon activity and butyrate production was enhanced in a physiologically relevant pH range. While the presence of the <i>arc</i> operon altered community dynamics, it did not impact production of short chain fatty acids. Dynamic computational modeling of pH-mediated interactions reveals the quantitative contribution of this mechanism to community assembly. In sum, our framework to quantify the contribution of molecular pathways and mechanism modalities on microbial community dynamics and functions could be applied more broadly.</p>","PeriodicalId":16480,"journal":{"name":"Journal of Nervous and Mental Disease","volume":"94 1","pages":""},"PeriodicalIF":1.6000,"publicationDate":"2024-04-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10659395/pdf/","citationCount":"0","resultStr":"{\"title\":\"Shaping human gut community assembly and butyrate production by controlling the arginine dihydrolase pathway.\",\"authors\":\"Yiyi Liu, Yu-Yu Cheng, Jaron Thompson, Zhichao Zhou, Eugenio I Vivas, Matthew F Warren, Federico E Rey, Karthik Anantharaman, Ophelia S Venturelli\",\"doi\":\"10.1101/2023.01.10.523442\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The arginine dihydrolase pathway (<i>arc</i> operon) present in a subset of diverse human gut species enables arginine catabolism. This specialized metabolic pathway can alter environmental pH and nitrogen availability, which in turn could shape gut microbiota inter-species interactions. By exploiting synthetic control of gene expression, we investigated the role of the <i>arc</i> operon in probiotic <i>Escherichia coli</i> Nissle 1917 on human gut community assembly and health-relevant metabolite profiles <i>in vitro</i> and in the murine gut. By stabilizing environmental pH, the <i>arc</i> operon reduced variability in community composition across different initial pH perturbations. The abundance of butyrate producing bacteria were altered in response to <i>arc</i> operon activity and butyrate production was enhanced in a physiologically relevant pH range. While the presence of the <i>arc</i> operon altered community dynamics, it did not impact production of short chain fatty acids. Dynamic computational modeling of pH-mediated interactions reveals the quantitative contribution of this mechanism to community assembly. In sum, our framework to quantify the contribution of molecular pathways and mechanism modalities on microbial community dynamics and functions could be applied more broadly.</p>\",\"PeriodicalId\":16480,\"journal\":{\"name\":\"Journal of Nervous and Mental Disease\",\"volume\":\"94 1\",\"pages\":\"\"},\"PeriodicalIF\":1.6000,\"publicationDate\":\"2024-04-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10659395/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Nervous and Mental Disease\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1101/2023.01.10.523442\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Nervous and Mental Disease","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1101/2023.01.10.523442","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
Shaping human gut community assembly and butyrate production by controlling the arginine dihydrolase pathway.
The arginine dihydrolase pathway (arc operon) present in a subset of diverse human gut species enables arginine catabolism. This specialized metabolic pathway can alter environmental pH and nitrogen availability, which in turn could shape gut microbiota inter-species interactions. By exploiting synthetic control of gene expression, we investigated the role of the arc operon in probiotic Escherichia coli Nissle 1917 on human gut community assembly and health-relevant metabolite profiles in vitro and in the murine gut. By stabilizing environmental pH, the arc operon reduced variability in community composition across different initial pH perturbations. The abundance of butyrate producing bacteria were altered in response to arc operon activity and butyrate production was enhanced in a physiologically relevant pH range. While the presence of the arc operon altered community dynamics, it did not impact production of short chain fatty acids. Dynamic computational modeling of pH-mediated interactions reveals the quantitative contribution of this mechanism to community assembly. In sum, our framework to quantify the contribution of molecular pathways and mechanism modalities on microbial community dynamics and functions could be applied more broadly.
期刊介绍:
The Journal of Nervous and Mental Disease publishes peer-reviewed articles containing new data or ways of reorganizing established knowledge relevant to understanding and modifying human behavior, especially that defined as impaired or diseased, and the context, applications and effects of that knowledge. Our policy is summarized by the slogan, "Behavioral science for clinical practice." We consider articles that include at least one behavioral variable, clear definition of study populations, and replicable research designs. Authors should use the active voice and first person whenever possible.