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基于 CRISPR-Cas 的抗菌剂:设计、挑战和细菌耐药机制。

CRISPR-Cas-Based Antimicrobials: Design, Challenges, and Bacterial Mechanisms of Resistance.

机构信息

Centro de Investigación Biomédica (CENBIO), Facultad de Ciencias de la Salud Eugenio Espejo, Universidad UTE, Quito 170527, Ecuador.

Escuela de Medicina, Colegio de Ciencias de la Salud Quito, Universidad San Francisco de Quito USFQ, Quito 170902, Ecuador.

出版信息

ACS Infect Dis. 2023 Jul 14;9(7):1283-1302. doi: 10.1021/acsinfecdis.2c00649. Epub 2023 Jun 22.

DOI:10.1021/acsinfecdis.2c00649
PMID:37347230
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10353011/
Abstract

The emergence of antibiotic-resistant bacterial strains is a source of public health concern across the globe. As the discovery of new conventional antibiotics has stalled significantly over the past decade, there is an urgency to develop novel approaches to address drug resistance in infectious diseases. The use of a CRISPR-Cas-based system for the precise elimination of targeted bacterial populations holds promise as an innovative approach for new antimicrobial agent design. The CRISPR-Cas targeting system is celebrated for its high versatility and specificity, offering an excellent opportunity to fight antibiotic resistance in pathogens by selectively inactivating genes involved in antibiotic resistance, biofilm formation, pathogenicity, virulence, or bacterial viability. The CRISPR-Cas strategy can enact antimicrobial effects by two approaches: inactivation of chromosomal genes or curing of plasmids encoding antibiotic resistance. In this Review, we provide an overview of the main CRISPR-Cas systems utilized for the creation of these antimicrobials, as well as highlighting promising studies in the field. We also offer a detailed discussion about the most commonly used mechanisms for CRISPR-Cas delivery: bacteriophages, nanoparticles, and conjugative plasmids. Lastly, we address possible mechanisms of interference that should be considered during the intelligent design of these novel approaches.

摘要

抗生素耐药菌的出现是全球公共卫生关注的一个来源。由于在过去十年中,新的常规抗生素的发现显著停滞不前,因此迫切需要开发新的方法来解决传染病中的耐药性问题。基于 CRISPR-Cas 的系统用于精确消除靶向细菌种群,有望成为新抗菌剂设计的创新方法。CRISPR-Cas 靶向系统以其高度的多功能性和特异性而著称,为通过选择性失活与抗生素耐药性、生物膜形成、致病性、毒力或细菌活力相关的基因来对抗病原体中的抗生素耐药性提供了极好的机会。CRISPR-Cas 策略可以通过两种方法发挥抗菌作用:染色体基因失活或消除编码抗生素耐药性的质粒。在这篇综述中,我们概述了用于创建这些抗菌药物的主要 CRISPR-Cas 系统,并强调了该领域有前途的研究。我们还详细讨论了 CRISPR-Cas 传递最常用的机制:噬菌体、纳米颗粒和可接合质粒。最后,我们讨论了在这些新方法的智能设计过程中应考虑的可能的干扰机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3a5/10353011/c87e721ea506/id2c00649_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3a5/10353011/4b415218275f/id2c00649_0001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3a5/10353011/45e86a9d3d5d/id2c00649_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3a5/10353011/62dc300cde71/id2c00649_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3a5/10353011/c87e721ea506/id2c00649_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3a5/10353011/4b415218275f/id2c00649_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3a5/10353011/57d36cc76f83/id2c00649_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3a5/10353011/ecaffca748bd/id2c00649_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3a5/10353011/45e86a9d3d5d/id2c00649_0004.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3a5/10353011/c87e721ea506/id2c00649_0006.jpg

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CRISPR-Cas System: A Tool to Eliminate Drug-Resistant Gram-Negative Bacteria.
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