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利用移动的、广谱宿主范围的 CRISPR-Cas9 递送工具去除 AMR 质粒。

Removal of AMR plasmids using a mobile, broad host-range CRISPR-Cas9 delivery tool.

机构信息

Centre for Ecology and Conservation, University of Exeter, Environment and Sustainability Institute, Penryn, TR10 9FE, UK.

Institute of Hydrobiology, Technische Universität Dresden, 01217 Dresden, Germany.

出版信息

Microbiology (Reading). 2023 May;169(5). doi: 10.1099/mic.0.001334.

Abstract

Antimicrobial resistance (AMR) genes are widely disseminated on plasmids. Therefore, interventions aimed at blocking plasmid uptake and transfer may curb the spread of AMR. Previous studies have used CRISPR-Cas-based technology to remove plasmids encoding AMR genes from target bacteria, using either phage- or plasmid-based delivery vehicles that typically have narrow host ranges. To make this technology feasible for removal of AMR plasmids from multiple members of complex microbial communities, an efficient, broad host-range delivery vehicle is needed. We engineered the broad host-range IncP1-plasmid pKJK5 to encode programmed to target an AMR gene. We demonstrate that the resulting plasmid pKJK5::csg has the ability to block the uptake of AMR plasmids and to remove resident plasmids from . Furthermore, due to its broad host range, pKJK5::csg successfully blocked AMR plasmid uptake in a range of environmental, pig- and human-associated coliform isolates, as well as in isolates of two species of . This study firmly establishes pKJK5::csg as a promising broad host-range CRISPR-Cas9 delivery tool for AMR plasmid removal, which has the potential to be applied in complex microbial communities to remove AMR genes from a broad range of bacterial species.

摘要

抗生素耐药性 (AMR) 基因广泛存在于质粒上。因此,旨在阻断质粒摄取和转移的干预措施可能会抑制 AMR 的传播。先前的研究已经使用基于 CRISPR-Cas 的技术来去除编码 AMR 基因的质粒,使用基于噬菌体或质粒的递送载体,这些载体通常宿主范围较窄。为了使这项技术能够从复杂微生物群落的多个成员中去除 AMR 质粒,需要一种高效、广谱的递送载体。我们设计了广谱的 IncP1 质粒 pKJK5 来编码一种靶向 AMR 基因的 CRISPR-Cas9 系统。我们证明,由此产生的质粒 pKJK5::csg 具有阻断 AMR 质粒摄取和去除 中常驻质粒的能力。此外,由于其广谱宿主范围,pKJK5::csg 成功阻断了一系列环境、猪和人相关大肠埃希菌分离株以及两种 分离株中 AMR 质粒的摄取。这项研究确立了 pKJK5::csg 作为一种有前途的广谱 CRISPR-Cas9 递送工具,可用于去除 AMR 质粒,有可能在复杂的微生物群落中应用,从广泛的细菌物种中去除 AMR 基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/315d/10268836/f6501ec59c9e/mic-169-01334-g001.jpg

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