Jiabao Xing , Hang Zhang , Leyin Zheng , Jinxin Zhao , Yuying Zhang , Zhiying Xu , Yajun Zhai , Gongzheng Hu , Jian Li , Hua Wu
{"title":"噬菌体治疗肺炎克雷伯菌:一个不断发展的观点","authors":"Jiabao Xing , Hang Zhang , Leyin Zheng , Jinxin Zhao , Yuying Zhang , Zhiying Xu , Yajun Zhai , Gongzheng Hu , Jian Li , Hua Wu","doi":"10.1016/j.biotechadv.2025.108689","DOIUrl":null,"url":null,"abstract":"<div><div><em>Klebsiella pneumoniae</em> represents one of the most concerning ESKAPE pathogens, with multidrug-resistant strains driving urgent clinical interest in phage therapy as a viable alternative to antibiotics. However, the evolutionary arms race between phages and bacteria has equipped <em>K. pneumoniae</em> with sophisticated anti-phage immune defenses, posing a substantial barrier to durable therapeutic success. Through systematic analysis of <em>K. pneumoniae</em>-phage co-evolutionary dynamics, we identify predominant resistance mechanisms and discuss why these mechanisms primarily concentrate on adsorption blocking pathways. We then integrate clinical case studies with preclinical research to evaluate combination strategies against phage resistance, particularly highlighting synergistic approaches using antibiotics-phage or phage cocktails/phage serial therapy that increase selective pressure while reducing bacterial host adaptability and pathogenicity. Finally, we propose a computational roadmap leveraging machine learning for phage characterization, host-interaction prediction and <em>de novo</em> genome engineering, with particular emphasis on minimizing resistance emergence. This interdisciplinary review provides both immediate clinical guidance and a forward-looking vision for rational phage design, applicable beyond not only to <em>K. pneumoniae</em> but also to other high-priority pathogens. We also highlight that integrations of synthetic biology, computational science, and microbiology will be essential for transitioning phage therapy from experimental treatments to standardized interventions addressing antimicrobial resistance.</div></div>","PeriodicalId":8946,"journal":{"name":"Biotechnology advances","volume":"84 ","pages":"Article 108689"},"PeriodicalIF":12.5000,"publicationDate":"2025-08-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Phage therapy against Klebsiella pneumoniae: An evolving perspective\",\"authors\":\"Jiabao Xing , Hang Zhang , Leyin Zheng , Jinxin Zhao , Yuying Zhang , Zhiying Xu , Yajun Zhai , Gongzheng Hu , Jian Li , Hua Wu\",\"doi\":\"10.1016/j.biotechadv.2025.108689\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div><em>Klebsiella pneumoniae</em> represents one of the most concerning ESKAPE pathogens, with multidrug-resistant strains driving urgent clinical interest in phage therapy as a viable alternative to antibiotics. However, the evolutionary arms race between phages and bacteria has equipped <em>K. pneumoniae</em> with sophisticated anti-phage immune defenses, posing a substantial barrier to durable therapeutic success. Through systematic analysis of <em>K. pneumoniae</em>-phage co-evolutionary dynamics, we identify predominant resistance mechanisms and discuss why these mechanisms primarily concentrate on adsorption blocking pathways. We then integrate clinical case studies with preclinical research to evaluate combination strategies against phage resistance, particularly highlighting synergistic approaches using antibiotics-phage or phage cocktails/phage serial therapy that increase selective pressure while reducing bacterial host adaptability and pathogenicity. Finally, we propose a computational roadmap leveraging machine learning for phage characterization, host-interaction prediction and <em>de novo</em> genome engineering, with particular emphasis on minimizing resistance emergence. This interdisciplinary review provides both immediate clinical guidance and a forward-looking vision for rational phage design, applicable beyond not only to <em>K. pneumoniae</em> but also to other high-priority pathogens. We also highlight that integrations of synthetic biology, computational science, and microbiology will be essential for transitioning phage therapy from experimental treatments to standardized interventions addressing antimicrobial resistance.</div></div>\",\"PeriodicalId\":8946,\"journal\":{\"name\":\"Biotechnology advances\",\"volume\":\"84 \",\"pages\":\"Article 108689\"},\"PeriodicalIF\":12.5000,\"publicationDate\":\"2025-08-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biotechnology advances\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0734975025001752\",\"RegionNum\":1,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOTECHNOLOGY & APPLIED MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biotechnology advances","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0734975025001752","RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
Phage therapy against Klebsiella pneumoniae: An evolving perspective
Klebsiella pneumoniae represents one of the most concerning ESKAPE pathogens, with multidrug-resistant strains driving urgent clinical interest in phage therapy as a viable alternative to antibiotics. However, the evolutionary arms race between phages and bacteria has equipped K. pneumoniae with sophisticated anti-phage immune defenses, posing a substantial barrier to durable therapeutic success. Through systematic analysis of K. pneumoniae-phage co-evolutionary dynamics, we identify predominant resistance mechanisms and discuss why these mechanisms primarily concentrate on adsorption blocking pathways. We then integrate clinical case studies with preclinical research to evaluate combination strategies against phage resistance, particularly highlighting synergistic approaches using antibiotics-phage or phage cocktails/phage serial therapy that increase selective pressure while reducing bacterial host adaptability and pathogenicity. Finally, we propose a computational roadmap leveraging machine learning for phage characterization, host-interaction prediction and de novo genome engineering, with particular emphasis on minimizing resistance emergence. This interdisciplinary review provides both immediate clinical guidance and a forward-looking vision for rational phage design, applicable beyond not only to K. pneumoniae but also to other high-priority pathogens. We also highlight that integrations of synthetic biology, computational science, and microbiology will be essential for transitioning phage therapy from experimental treatments to standardized interventions addressing antimicrobial resistance.
期刊介绍:
Biotechnology Advances is a comprehensive review journal that covers all aspects of the multidisciplinary field of biotechnology. The journal focuses on biotechnology principles and their applications in various industries, agriculture, medicine, environmental concerns, and regulatory issues. It publishes authoritative articles that highlight current developments and future trends in the field of biotechnology. The journal invites submissions of manuscripts that are relevant and appropriate. It targets a wide audience, including scientists, engineers, students, instructors, researchers, practitioners, managers, governments, and other stakeholders in the field. Additionally, special issues are published based on selected presentations from recent relevant conferences in collaboration with the organizations hosting those conferences.