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本文引用的文献

1
CRISPR/Cas Systems in Genome Editing: Methodologies and Tools for sgRNA Design, Off-Target Evaluation, and Strategies to Mitigate Off-Target Effects.基因组编辑中的CRISPR/Cas系统:sgRNA设计、脱靶评估方法及减轻脱靶效应的策略与工具
Adv Sci (Weinh). 2020 Feb 6;7(6):1902312. doi: 10.1002/advs.201902312. eCollection 2020 Mar.
2
A bacterial gene-drive system efficiently edits and inactivates a high copy number antibiotic resistance locus.一种细菌基因驱动系统可有效地编辑和失活高拷贝数抗生素抗性基因座。
Nat Commun. 2019 Dec 16;10(1):5726. doi: 10.1038/s41467-019-13649-6.
3
CRISPR-cas system: biological function in microbes and its use to treat antimicrobial resistant pathogens.CRISPR-cas 系统:微生物中的生物学功能及其在治疗抗微生物药物耐药性病原体中的应用。
Ann Clin Microbiol Antimicrob. 2019 Jul 5;18(1):21. doi: 10.1186/s12941-019-0317-x.
4
CRISPR-Cas antimicrobials: Challenges and future prospects.CRISPR-Cas抗菌剂:挑战与未来前景。
PLoS Pathog. 2018 Jun 14;14(6):e1006990. doi: 10.1371/journal.ppat.1006990. eCollection 2018 Jun.
5
CRISPR-Based Antibacterials: Transforming Bacterial Defense into Offense.基于 CRISPR 的抗菌剂:将细菌防御转化为进攻。
Trends Biotechnol. 2018 Feb;36(2):127-130. doi: 10.1016/j.tibtech.2017.10.021. Epub 2017 Nov 17.
6
Delivery strategies of the CRISPR-Cas9 gene-editing system for therapeutic applications.CRISPR-Cas9 基因编辑系统的治疗应用传递策略。
J Control Release. 2017 Nov 28;266:17-26. doi: 10.1016/j.jconrel.2017.09.012. Epub 2017 Sep 11.
7
To the G20: incentivising antibacterial research and development.致二十国集团:激励抗菌药物研发
Lancet Infect Dis. 2017 Aug;17(8):799-801. doi: 10.1016/S1473-3099(17)30404-8. Epub 2017 Jul 7.
8
CRISPR/Cas9-Based Genome Editing for Disease Modeling and Therapy: Challenges and Opportunities for Nonviral Delivery.基于 CRISPR/Cas9 的基因组编辑在疾病建模和治疗中的应用:非病毒递送的挑战和机遇。
Chem Rev. 2017 Aug 9;117(15):9874-9906. doi: 10.1021/acs.chemrev.6b00799. Epub 2017 Jun 22.
9
Next-generation precision antimicrobials: towards personalized treatment of infectious diseases.下一代精准抗菌药物:迈向传染病的个体化治疗。
Curr Opin Microbiol. 2017 Jun;37:95-102. doi: 10.1016/j.mib.2017.05.014. Epub 2017 Jun 14.
10
Healthy human gut phageome.健康人类肠道噬菌体组
Proc Natl Acad Sci U S A. 2016 Sep 13;113(37):10400-5. doi: 10.1073/pnas.1601060113. Epub 2016 Aug 29.

CRISPR-Cas 系统:应对抗生素耐药性的潜在替代工具。

CRISPR-Cas system: a potential alternative tool to cope antibiotic resistance.

机构信息

Biomedical Research Center, Northwest Minzu University, Lanzhou, 730030, P. R. China.

Department of Microbiology, Government College University Faisalabad, Faisalabad, Pakistan.

出版信息

Antimicrob Resist Infect Control. 2020 Aug 10;9(1):131. doi: 10.1186/s13756-020-00795-6.

DOI:10.1186/s13756-020-00795-6
PMID:32778162
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7418376/
Abstract

Antibiotic exposure leads to massive selective pressures that initiate the emergence and spread of antibiotic resistance in commensal and pathogenic bacteria. The slow process of developing new antibiotics makes this approach counterintuitive for combatting the rapid emergence of new antibiotic resistant pathogens. Therefore, alternative approaches such as, the development of nucleic acid-based anti-bacterial treatments, anti-bacterial peptides, bacteriocins, anti-virulence compounds and bacteriophage therapies should be exploited to cope infections caused by resistant superbugs. In this editorial, we discuss how the newly popular CRISPR-Cas system has been applied to combat antibiotic resistance.

摘要

抗生素暴露会导致巨大的选择性压力,从而引发共生菌和病原菌中抗生素耐药性的出现和传播。开发新抗生素的缓慢过程使得这种方法在对抗新出现的抗生素耐药性病原体方面具有反直觉性。因此,应该利用基于核酸的抗菌治疗、抗菌肽、细菌素、抗毒化合物和噬菌体疗法等替代方法来应对耐药超级细菌引起的感染。在这篇社论中,我们讨论了新流行的 CRISPR-Cas 系统如何被应用于对抗抗生素耐药性。