Marina Athanasouli, Tobias Loschko, Christian Roedelsperger
{"title":"种间系统生物学将细菌代谢途径与线虫基因表达、趋化行为和生存联系起来","authors":"Marina Athanasouli, Tobias Loschko, Christian Roedelsperger","doi":"10.1101/gr.280848.125","DOIUrl":null,"url":null,"abstract":"All animals live in tight association with complex microbial communities, yet studying the effects of individual bacteria remains challenging. Bacterial feeding nematodes are powerful systems to study host microbe interactions as worms can be grown on monoxenic cultures. Here, we present three different types of resources that may assist future research of cross-species interactions in the nematode <em>Pristionchus pacificus</em>, but also in other organisms. First, by sequencing the genomes of 84 <em>Pristionchus</em>-associated bacteria, we establish a genomic basis to study host microbe interactions and we demonstrate its utility to identify candidate pathways in the bacteria affecting chemotaxis behavior and survival in the nematodes. Second, we generated nematode transcriptomes of <em>P. pacificus</em> nematodes on 38 bacterial diets and characterized 60 coexpression modules with differential responses to environmental microbiota. Third, we link the microbial genome and host transcriptome data by predicting a global map of more than 2,800 metabolic interactions. These interactions represent statistical associations between variation in bacterial metabolic potential and differential transcriptomic responses of coexpression modules in the nematode. Analysis of the interactome identifies several intestinal modules as the primary response layer to diverse microbiota and reveals a number of broadly conserved metabolic interactions. In summary, our study establishes a multiomic framework for future mechanistic studies in <em>P. pacificus</em> and may also be conceptually transferred and reimplemented in other organisms in order to investigate the evolution of the host microbe interactome.","PeriodicalId":12678,"journal":{"name":"Genome research","volume":"15 1","pages":""},"PeriodicalIF":5.5000,"publicationDate":"2025-08-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Interspecies systems biology links bacterial metabolic pathways to nematode gene expression, chemotaxis behavior, and survival\",\"authors\":\"Marina Athanasouli, Tobias Loschko, Christian Roedelsperger\",\"doi\":\"10.1101/gr.280848.125\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"All animals live in tight association with complex microbial communities, yet studying the effects of individual bacteria remains challenging. Bacterial feeding nematodes are powerful systems to study host microbe interactions as worms can be grown on monoxenic cultures. Here, we present three different types of resources that may assist future research of cross-species interactions in the nematode <em>Pristionchus pacificus</em>, but also in other organisms. First, by sequencing the genomes of 84 <em>Pristionchus</em>-associated bacteria, we establish a genomic basis to study host microbe interactions and we demonstrate its utility to identify candidate pathways in the bacteria affecting chemotaxis behavior and survival in the nematodes. Second, we generated nematode transcriptomes of <em>P. pacificus</em> nematodes on 38 bacterial diets and characterized 60 coexpression modules with differential responses to environmental microbiota. Third, we link the microbial genome and host transcriptome data by predicting a global map of more than 2,800 metabolic interactions. These interactions represent statistical associations between variation in bacterial metabolic potential and differential transcriptomic responses of coexpression modules in the nematode. Analysis of the interactome identifies several intestinal modules as the primary response layer to diverse microbiota and reveals a number of broadly conserved metabolic interactions. In summary, our study establishes a multiomic framework for future mechanistic studies in <em>P. pacificus</em> and may also be conceptually transferred and reimplemented in other organisms in order to investigate the evolution of the host microbe interactome.\",\"PeriodicalId\":12678,\"journal\":{\"name\":\"Genome research\",\"volume\":\"15 1\",\"pages\":\"\"},\"PeriodicalIF\":5.5000,\"publicationDate\":\"2025-08-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Genome research\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1101/gr.280848.125\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Genome research","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1101/gr.280848.125","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Interspecies systems biology links bacterial metabolic pathways to nematode gene expression, chemotaxis behavior, and survival
All animals live in tight association with complex microbial communities, yet studying the effects of individual bacteria remains challenging. Bacterial feeding nematodes are powerful systems to study host microbe interactions as worms can be grown on monoxenic cultures. Here, we present three different types of resources that may assist future research of cross-species interactions in the nematode Pristionchus pacificus, but also in other organisms. First, by sequencing the genomes of 84 Pristionchus-associated bacteria, we establish a genomic basis to study host microbe interactions and we demonstrate its utility to identify candidate pathways in the bacteria affecting chemotaxis behavior and survival in the nematodes. Second, we generated nematode transcriptomes of P. pacificus nematodes on 38 bacterial diets and characterized 60 coexpression modules with differential responses to environmental microbiota. Third, we link the microbial genome and host transcriptome data by predicting a global map of more than 2,800 metabolic interactions. These interactions represent statistical associations between variation in bacterial metabolic potential and differential transcriptomic responses of coexpression modules in the nematode. Analysis of the interactome identifies several intestinal modules as the primary response layer to diverse microbiota and reveals a number of broadly conserved metabolic interactions. In summary, our study establishes a multiomic framework for future mechanistic studies in P. pacificus and may also be conceptually transferred and reimplemented in other organisms in order to investigate the evolution of the host microbe interactome.
期刊介绍:
Launched in 1995, Genome Research is an international, continuously published, peer-reviewed journal that focuses on research that provides novel insights into the genome biology of all organisms, including advances in genomic medicine.
Among the topics considered by the journal are genome structure and function, comparative genomics, molecular evolution, genome-scale quantitative and population genetics, proteomics, epigenomics, and systems biology. The journal also features exciting gene discoveries and reports of cutting-edge computational biology and high-throughput methodologies.
New data in these areas are published as research papers, or methods and resource reports that provide novel information on technologies or tools that will be of interest to a broad readership. Complete data sets are presented electronically on the journal''s web site where appropriate. The journal also provides Reviews, Perspectives, and Insight/Outlook articles, which present commentary on the latest advances published both here and elsewhere, placing such progress in its broader biological context.