药品
微生物群
生物
敏化
背景(考古学)
生物累积
肠道菌群
微生物种群生物学
药理学
生态学
细菌
免疫学
生物信息学
遗传学
古生物学
作者
Sarela García‐Santamarina,Michael Kuhn,Saravanan Devendran,Lisa Maier,Marja Driessen,André Mateus,Eleonora Mastrorilli,Ana Rita Brochado,Mikhail M. Savitski,Kiran Raosaheb Patil,Michael Zimmermann,Peer Bork,Athanasios Typas
标识
DOI:10.1101/2023.06.13.544832
摘要
Summary Pharmaceuticals can directly inhibit the growth of gut bacteria, but the degree such interactions manifest in complex community settings is an open question. Here we compared the effects of 30 drugs on a 32-species synthetic community with their effects on each community member in isolation. While most individual drug–species interactions remained the same in the community context, communal behaviors emerged in 26% of all tested cases. Cross-protection, during which drug-sensitive species became protected in community, was 6-times more frequent than cross-sensitization, the converse phenomenon. Cross-protection decreased and cross-sensitization increased at higher drug concentrations, suggesting that the resilience of microbial communities can collapse when perturbations get stronger. By metabolically profiling drug-treated communities, we showed that both drug biotransformation and bioaccumulation contribute mechanistically to communal protection. As a proof-of-principle, we molecularly dissected a prominent case: species expressing specific nitroreductases degraded niclosamide, thereby protecting both themselves and sensitive community members.
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