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金属β-内酰胺酶的系统发育更新。

An updated phylogeny of the metallo-β-lactamases.

机构信息

Department of Mathematical Sciences, Chalmers University of Technology and University of Gothenburg, Gothenburg, Sweden.

Centre for Antibiotic Resistance Research (CARe), University of Gothenburg, Gothenburg, Sweden.

出版信息

J Antimicrob Chemother. 2021 Jan 1;76(1):117-123. doi: 10.1093/jac/dkaa392.

Abstract

BACKGROUND

Metallo-β-lactamases (MBLs) are enzymes that use zinc-dependent hydrolysis to confer resistance to almost all available β-lactam antibiotics. They are hypothesized to originate from commensal and environmental bacteria, from where some have mobilized and transferred horizontally to pathogens. The current phylogeny of MBLs, however, is biased as it is founded largely on genes encountered in pathogenic bacteria. This incompleteness is emphasized by recent findings of environmental MBLs with new forms of zinc binding sites and atypical functional profiles.

OBJECTIVES

To expand the phylogeny of MBLs to provide a more accurate view of their evolutionary history.

METHODS

We searched more than 16 terabases of genomic and metagenomic data for MBLs of the three subclasses B1, B2 and B3 using the validated fARGene method. Predicted genes, together with the previously known ones, were used to infer phylogenetic trees.

RESULTS

We identified 2290 unique MBL genes forming 817 gene families, of which 741 were previously uncharacterized. MBLs from subclasses B1 and B3 separated into distinct monophyletic groups, in agreement with their taxonomic and functional properties. We present evidence that clinically associated MBLs were mobilized from Proteobacteria. Additionally, we identified three new variants of the zinc binding sites, indicating that the functional repertoire is broader than previously reported.

CONCLUSIONS

Based on our results, we recommend that the nomenclature of MBLs is refined into the phylogenetic groups B1.1-B1.5 and B3.1-B3.4 that more accurately describe their molecular and functional characteristics. Our results will also facilitate the annotation of novel MBLs, reflecting their taxonomic organization and evolutionary origin.

摘要

背景

金属β-内酰胺酶(MBLs)是一种利用锌依赖性水解来赋予对几乎所有可用β-内酰胺抗生素的抗性的酶。它们被认为起源于共生和环境细菌,其中一些已经发生了移动并横向转移到病原体中。然而,目前的 MBL 系统发育是有偏见的,因为它主要基于在病原体中遇到的基因。这种不完整性被最近发现的具有新形式锌结合位点和非典型功能特征的环境 MBL 所强调。

目的

扩展 MBL 的系统发育,以更准确地了解其进化历史。

方法

我们使用经过验证的 fARGene 方法,在超过 16 太字节的基因组和宏基因组数据中搜索了三类 B1、B2 和 B3 的 MBL。预测的基因与以前已知的基因一起用于推断系统发育树。

结果

我们鉴定了 2290 个独特的 MBL 基因,形成了 817 个基因家族,其中 741 个是以前未描述的。B1 和 B3 亚类的 MBL 分为不同的单系群,与它们的分类学和功能特性一致。我们提供的证据表明,与临床相关的 MBL 是从变形菌门中移动来的。此外,我们还鉴定了三个新的锌结合位点变体,表明功能谱比以前报道的更广泛。

结论

基于我们的结果,我们建议将 MBL 的命名法细化为更准确描述其分子和功能特征的 B1.1-B1.5 和 B3.1-B3.4 分类群。我们的结果还将有助于对新型 MBL 的注释,反映它们的分类组织和进化起源。

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