生成语法
溶解循环
噬菌体
计算生物学
合成生物学
计算机科学
基因组
细菌基因组大小
生成模型
蓝图
基因组工程
编码
溶原循环
选择(遗传算法)
设计要素和原则
DNA测序
生物
人工智能
生成设计
比例(比率)
长尾病毒科
基因组学
整合酶
进化生物学
生命系统
生物进化
原核生物
遗传学
作者
S. B. King,C. Driscoll,David Li,Daniel Guo,Aditi Merchant,Garyk Brixi,Max E. Wilkinson,Brian Hie
出处
期刊:
[Cold Spring Harbor Laboratory]
日期:2025-09-17
被引量:28
标识
DOI:10.1101/2025.09.12.675911
摘要
Abstract Many important biological functions arise not from single genes, but from complex interactions encoded by entire genomes. Genome language models have emerged as a promising strategy for designing biological systems, but their ability to generate functional sequences at the scale of whole genomes has remained untested. Here, we report the first generative design of viable bacteriophage genomes. We leveraged frontier genome language models, Evo 1 and Evo 2, to generate whole-genome sequences with realistic genetic architectures and desirable host tropism, using the lytic phage ΦX174 as our design template. Experimental testing of AI-generated genomes yielded 16 viable phages with substantial evolutionary novelty. Cryo-electron microscopy revealed that one of the generated phages utilizes an evolutionarily distant DNA packaging protein within its capsid. Multiple phages demonstrate higher fitness than ΦX174 in growth competitions and in their lysis kinetics. A cocktail of the generated phages rapidly overcomes ΦX174-resistance in three E. coli strains, demonstrating the potential utility of our approach for designing phage therapies against rapidly evolving bacterial pathogens. This work provides a blueprint for the design of diverse synthetic bacteriophages and, more broadly, lays a foundation for the generative design of useful living systems at the genome scale.
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