生物
微生物群
计算生物学
生物信息学
选择(遗传算法)
基因组
功能(生物学)
加权
编码
合成生物学
生化工程
人体微生物群
蛋白质组
人类疾病
共同进化
机制(生物学)
遗传学
微生物生态学
系统生物学
生物信息学
肠道微生物群
炎症性肠病
进化生物学
环境生物技术
钥匙(锁)
否定选择
炎症性肠病
代谢组学
微生物种群生物学
定向分子进化
拉伤
模式生物
适应(眼睛)
生态学
选型
疾病
作者
Thomas C. A. Hitch,J. F. van den Bosch,Silvia Bolsega,Charlotte Deschamps,Lucie Etienne‐Mesmin,Nicole Treichel,Stéphanie Blanquet‐Diot,Soeren Ocvirk,Marijana Basic,Thomas Clavel
标识
DOI:10.1093/ismejo/wraf209
摘要
Understanding the complex interactions between microbes and their environment requires robust model systems such as synthetic communities (SynComs). We developed a functionally directed approach to generate SynComs by selecting strains that encode key functions identified in metagenomes. This approach enables the rapid construction of SynComs tailored to any ecosystem. To optimize community design, we implemented genome-scale metabolic models, providing in silico evidence for cooperative strain coexistence prior to experimental validation. Using this strategy, we designed multiple host-specific SynComs, including those for the rumen, mouse, and human microbiomes. By weighting functions differentially enriched in diseased versus healthy individuals, we constructed SynComs that capture complex host-microbe interactions. We designed an inflammatory bowel disease SynCom of 10 members that successfully induced colitis in gnotobiotic IL10-/- mice, demonstrating the potential of this method to model disease-associated microbiomes. Our study establishes a framework for designing functionally representative SynComs of any microbial ecosystem, facilitating mechanistic study.
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