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金黄色葡萄球菌噬菌体宿主细胞识别和穿透机制的结构。

Structure of the host cell recognition and penetration machinery of a Staphylococcus aureus bacteriophage.

机构信息

Department of Microbiology, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.

Structural Virology Section, Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, United States of America.

出版信息

PLoS Pathog. 2020 Feb 18;16(2):e1008314. doi: 10.1371/journal.ppat.1008314. eCollection 2020 Feb.

Abstract

Staphylococcus aureus is a common cause of infections in humans. The emergence of virulent, antibiotic-resistant strains of S. aureus is a significant public health concern. Most virulence and resistance factors in S. aureus are encoded by mobile genetic elements, and transduction by bacteriophages represents the main mechanism for horizontal gene transfer. The baseplate is a specialized structure at the tip of bacteriophage tails that plays key roles in host recognition, cell wall penetration, and DNA ejection. We have used high-resolution cryo-electron microscopy to determine the structure of the S. aureus bacteriophage 80α baseplate at 3.75 Å resolution, allowing atomic models to be built for most of the major tail and baseplate proteins, including two tail fibers, the receptor binding protein, and part of the tape measure protein. Our structure provides a structural basis for understanding host recognition, cell wall penetration and DNA ejection in viruses infecting Gram-positive bacteria. Comparison to other phages demonstrates the modular design of baseplate proteins, and the adaptations to the host that take place during the evolution of staphylococci and other pathogens.

摘要

金黄色葡萄球菌是人类感染的常见原因。具有毒力、抗药性的金黄色葡萄球菌菌株的出现是一个重大的公共卫生关注问题。金黄色葡萄球菌中的大多数毒力和抗性因素是由可移动遗传因子编码的,噬菌体转导是水平基因转移的主要机制。基板是噬菌体尾部尖端的一种特殊结构,在宿主识别、细胞壁穿透和 DNA 喷射中起着关键作用。我们使用高分辨率冷冻电子显微镜以 3.75Å 的分辨率确定了金黄色葡萄球菌噬菌体 80α 基板的结构,从而可以为大多数主要的尾部和基板蛋白构建原子模型,包括两个尾纤维、受体结合蛋白和部分量尺蛋白。我们的结构为理解感染革兰氏阳性菌的病毒的宿主识别、细胞壁穿透和 DNA 喷射提供了结构基础。与其他噬菌体的比较表明了基板蛋白的模块化设计,以及在金黄色葡萄球菌和其他病原体的进化过程中发生的对宿主的适应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b5c/7048315/bc49baad38c8/ppat.1008314.g001.jpg

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