热应激诱导肠杆菌科噬菌体耐受。

IF 6.4 1区 生物学 Q1 BIOLOGY
eLife Pub Date : 2025-07-07 DOI:10.7554/eLife.105703
Fan Zhang, Hao-Ze Chen, Bo Zheng, Liang Huang, Ye Xiang, Jing-Ren Zhang, Jia-Feng Liu
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引用次数: 0

摘要

抗生素耐药性和耐受性是全球医疗保健面临的重大挑战,需要采用噬菌体治疗等替代策略。然而,抗噬菌体突变体的迅速出现带来了潜在的风险。本文以肺炎克雷伯菌ATCC 43816及其裂解噬菌体Kp11为模型系统,研究了细菌对噬菌体的持久性,其特征是异质生存,类似于抗生素的持久性。我们发现,热处理增强了噬菌体暴露下细菌的持久性和存活率,随后促进了噬菌体耐药性的进化。进一步的实验表明,热应激导致包膜成分减少,从而抑制噬菌体DNA注射。此外,这种热诱导的减少导致包膜应激反应的系统性改变,使细菌对抗生素多粘菌素耐受,同时使它们对pH值变化和免疫清除过敏。我们的发现为噬菌体相互作用提供了新的见解,并强调了在临床环境中实施噬菌体治疗的潜在挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Heat stress induces phage tolerance in Enterobacteriaceae.

Antibiotic resistance and tolerance present significant challenges in global healthcare, necessitating alternative strategies such as phage therapy. However, the rapid emergence of phage-resistant mutants poses a potential risk. Here, using Klebsiella pneumoniae ATCC 43816 and its lytic phage Kp11 as a model system, we investigated bacterial persistence against phages, characterized by heterogeneous survival, analogous to antibiotic persistence. We found that heat treatment enhanced persistence and increased bacterial survival under phage exposure, subsequently promoting the evolution of phage resistance. Further experiments demonstrated that heat stress leads to a reduction in envelope components, thereby inhibiting phage DNA injection. Additionally, this heat-induced reduction resulted in systematic alterations in envelope stress responses, rendering bacteria tolerant to the antibiotic polymyxin while making them hypersensitive to pH changes and immune clearance. Our findings provide novel insights into bacteria-phage interactions and highlight potential challenges in implementing phage therapy in clinical settings.

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来源期刊
eLife
eLife BIOLOGY-
CiteScore
12.90
自引率
3.90%
发文量
3122
审稿时长
17 weeks
期刊介绍: eLife is a distinguished, not-for-profit, peer-reviewed open access scientific journal that specializes in the fields of biomedical and life sciences. eLife is known for its selective publication process, which includes a variety of article types such as: Research Articles: Detailed reports of original research findings. Short Reports: Concise presentations of significant findings that do not warrant a full-length research article. Tools and Resources: Descriptions of new tools, technologies, or resources that facilitate scientific research. Research Advances: Brief reports on significant scientific advancements that have immediate implications for the field. Scientific Correspondence: Short communications that comment on or provide additional information related to published articles. Review Articles: Comprehensive overviews of a specific topic or field within the life sciences.
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