北京化工大学生命科学与技术学院 北京 100029
[ "陈青黎(2000—),女,硕士研究生。研究方向为合成生物学改造工程噬菌体。E-mail:ql.chen@buct.edu.cn" ]
[ "童贻刚(1966—),男,研究员,博士生导师。研究方向为噬菌体学、微生物学、高通量测序、生物信息学研究、合成生物学等。E-mail:tongyigang@mail.buct.edu.cn" ]
收稿:2022-12-06,
修回:2022-12-30,
纸质出版:2023-04-30
移动端阅览
陈青黎, 童贻刚. 工程噬菌体的合成生物学“智造”[J]. 合成生物学, 2023, 4(2): 283-300
CHEN Qingli, TONG Yigang. Merging the frontiers: synthetic biology for advanced bacteriophage design[J]. Synthetic Biology Journal, 2023, 4(2): 283-300
陈青黎, 童贻刚. 工程噬菌体的合成生物学“智造”[J]. 合成生物学, 2023, 4(2): 283-300 DOI: 10.12211/2096-8280.2022-070.
CHEN Qingli, TONG Yigang. Merging the frontiers: synthetic biology for advanced bacteriophage design[J]. Synthetic Biology Journal, 2023, 4(2): 283-300 DOI: 10.12211/2096-8280.2022-070.
噬菌体,以杀菌特性而闻名的天然病毒,是地球上多样性和丰度最高的生物体。在过去100多年中,噬菌体的研究极大地推动了遗传学、分子生物学和合成生物学的发展。随着耐药超级细菌的流行,噬菌体疗法引人入胜的科学历史也被广为传颂。然而,相对于自然环境中丰富的噬菌体数量(总数为10
31
,比所有其他生物的总和还要多),目前只有少数噬菌体成功应用于对抗耐药性细菌感染及其他工程领域。当前,急需践行合成生物学从“造物致知”到“造物致用”理念,采用高通量测序和基因组精准编辑等先进生物技术来创建具有独特属性的增强变体,提高噬菌体治疗的疗效和可编程性。本文综述了近年来噬菌体基因工程改造方法的技术进展以及合成生物学助力噬菌体应用技术发展的研究动态,如按照实际需求改造噬菌体宿主范围、借助宏基因组挖掘自然界中噬菌体的广泛资源、结合多组学技术揭示噬菌体与宿主互作的分子机制、调控肠道噬菌体组维持肠道稳态以促进人体健康及利用大数据和新型人工智能指导噬菌体理性设计。总之,合成生物学正在跨时代驱动传统实验研究范式转变,结合“设计—构建—测试—学习(DBTL)循环”理性设计目标噬菌体,无论是自上而下的体系优化,还是自下而上的生命体重构,工程噬菌体的合成生物学“智造”都大有可为。
Bacteriophages (phages)
natural viruses known for infecting and killing bacteria
are the most diverse and abundant organisms on Earth. Within the past 100 years of research on phages
breakthroughs in genetics
molecular biology
and synthetic biology have been successfully achieved. The fascinating scientific history of phage therapy has been repeatedly reported
as drug-resistant bacteria are becoming increasingly prevalent. Although phages outnumber other species combined in nature (10
31
in total)
only a small fraction of them have been successfully exploited for fighting infections caused by drug-resistant bacteria. Therefore
there is an urgent need for implementing the motto of synthetic biology
"build to learn
build to use"
and also using methods such as high-throughput sequencing and precise genome editing to create enhanced variants with unique features
improving efficacy and programmability for phage therapy. In the review
we discuss recent technological advances in phage genome engineering approaches and the potential applications of synthetic biology to engineer phages
such as modifying the host range of phages for practical needs
mining the extensive resources of phages in nature with the help of macro genomes
combining multi-omics technologies to reveal molecular mechanisms underlying phage-host interactions
regulating intestinal phages to maintain intestinal homeostasis for human health
and using big data and artificial intelligence to guide rati
onal phage design. Synthetic biology is driving a paradigm shift in traditional experimental research by combining "Design-Build-Test-Learn (DBTL) cycles" to rational design for phages
making synthetically designed phages promising for both top-down system optimization and bottom-up life-form reconstruction.
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