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蛋白质AmiA、AliA和AliB可结合在其他细菌物种核糖体蛋白中发现的肽段。

Proteins AmiA, AliA, and AliB Bind Peptides Found in Ribosomal Proteins of Other Bacterial Species.

作者信息

Nasher Fauzy, Heller Manfred, Hathaway Lucy J

机构信息

Institute for Infectious Diseases, Faculty of Medicine, University of Bern, Bern, Switzerland.

Graduate School for Cellular and Biomedical Sciences, University of Bern, Bern, Switzerland.

出版信息

Front Microbiol. 2018 Jan 15;8:2688. doi: 10.3389/fmicb.2017.02688. eCollection 2017.

DOI:10.3389/fmicb.2017.02688
PMID:29379482
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5775242/
Abstract

The nasopharynx is frequently colonized by both commensal and pathogenic bacteria including (pneumococcus). Pneumococcus is an important pathogen responsible for bacterial meningitis and community acquired pneumonia but is also commonly an asymptomatic colonizer of the nasopharynx. Understanding interactions between microbes may provide insights into pathogenesis. Here, we investigated the ability of the three oligopeptide-binding proteins AmiA, AliA, and AliB of an ATP-binding cassette transporter of pneumococcus to detect short peptides found in other bacterial species. We found three possible peptide ligands for AmiA and four each for AliA and AliB of which two for each protein matched ribosomal proteins of other bacterial species. Using synthetic peptides we confirmed the following binding: AmiA binds peptide AKTIKITQTR, matching 50S ribosomal subunit protein L30, AliA binds peptide FNEMQPIVDRQ, matching 30S ribosomal protein S20, and AliB binds peptide AIQSEKARKHN, matching 30S ribosomal protein S20, without excluding the possibility of binding of the other peptides. These Ami-AliA/AliB peptide ligands are found in multiple species in the class of Gammaproteobacteria which includes common colonizers of the nostrils and nasopharynx. Binding such peptides may enable pneumococcus to detect and respond to neighboring species in its environment and is a potential mechanism for interspecies communication and environmental surveillance.

摘要

鼻咽部经常被共生菌和致病菌定植,包括肺炎球菌。肺炎球菌是引起细菌性脑膜炎和社区获得性肺炎的重要病原体,但通常也是鼻咽部的无症状定植菌。了解微生物之间的相互作用可能有助于深入了解发病机制。在这里,我们研究了肺炎球菌ATP结合盒转运体的三种寡肽结合蛋白AmiA、AliA和AliB检测其他细菌物种中发现的短肽的能力。我们发现AmiA有三种可能的肽配体,AliA和AliB各有四种,其中每种蛋白各有两种与其他细菌物种的核糖体蛋白匹配。使用合成肽,我们证实了以下结合:AmiA结合肽AKTIKITQTR,与50S核糖体亚基蛋白L30匹配;AliA结合肽FNEMQPIVDRQ,与30S核糖体蛋白S20匹配;AliB结合肽AIQSEKARKHN,与30S核糖体蛋白S20匹配,但不排除其他肽结合的可能性。这些Ami-AliA/AliB肽配体存在于γ-变形菌纲的多个物种中,γ-变形菌纲包括鼻孔和鼻咽部的常见定植菌。结合这些肽可能使肺炎球菌能够检测并响应其环境中的邻近物种,这是种间通讯和环境监测的一种潜在机制。

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AmiA and AliA peptide ligands are secreted by Klebsiella pneumoniae and inhibit growth of Streptococcus pneumoniae.阿米 A 和阿利 A 肽配体由肺炎克雷伯菌分泌,并抑制肺炎链球菌的生长。
Sci Rep. 2022 Dec 23;12(1):22268. doi: 10.1038/s41598-022-26838-z.
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