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肠球菌-噬菌体相互作用的分子机制及其对人类健康的影响。

Molecular mechanisms of enterococcal-bacteriophage interactions and implications for human health.

机构信息

Department of Infectious Diseases, University of Colorado School of Medicine, Aurora, CO 80045, United States; Department of Immunology and Microbiology, University of Colorado School of Medicine, Aurora, CO 80045, United States.

Department of Immunology and Microbiology, University of Colorado School of Medicine, Aurora, CO 80045, United States.

出版信息

Curr Opin Microbiol. 2020 Aug;56:38-44. doi: 10.1016/j.mib.2020.06.003. Epub 2020 Jul 8.

DOI:10.1016/j.mib.2020.06.003
PMID:32652484
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7744351/
Abstract

Once overlooked as passive bystanders of the human intestinal microbiota, new evidence is shedding light on the importance of enterococci and their bacteriophages (phages) in shaping human health. Natural predators of enterococci, phages represent a narrow spectrum, precision targeting modality for the eradication of problematic enterococci within the microbiota or infected tissue. The identification of enterococcal phage receptors, absorption factors, and transcriptional responses following phage infection reveals a complex predator-prey relationship that modulates enterococcal cell surface architecture, susceptibility to antibiotics, and adaptation to host associated environments. Considering the dry up of contemporary antibiotic discovery pipelines in the pharmaceutical industry and a continued emergence of multidrug-resistant enterococci, enterococcal phages may serve as bonafide therapeutics. We highlight current advances in enterococcal phage biology with emphasis on recent breakthroughs in potential therapeutic applications that place enterococcal phages at the forefront of next-generation biologics.

摘要

曾经被忽视为人类肠道微生物群的被动旁观者,新的证据揭示了肠球菌及其噬菌体(噬菌体)在塑造人类健康方面的重要性。肠球菌的天然捕食者,噬菌体代表了一种窄谱、精准靶向的模式,可以在微生物群或感染组织内根除有问题的肠球菌。噬菌体感染后肠球菌噬菌体受体、吸收因子和转录反应的鉴定揭示了一种复杂的捕食者-猎物关系,这种关系调节肠球菌细胞表面结构、对抗生素的敏感性以及对宿主相关环境的适应性。考虑到制药行业当代抗生素发现管道的枯竭和多药耐药肠球菌的持续出现,肠球菌噬菌体可能成为真正的治疗药物。我们强调肠球菌噬菌体生物学的当前进展,重点介绍潜在治疗应用的最新突破,这些突破使肠球菌噬菌体处于下一代生物制剂的前沿。

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Nat Microbiol. 2020 Mar;5(3):465-472. doi: 10.1038/s41564-019-0634-z. Epub 2020 Feb 17.
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Lactose drives expansion to promote graft-versus-host disease.乳糖驱动扩张以促进移植物抗宿主病。
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