Al-Ouqaili Mushtak T S, Ahmad Amna, Jwair Noor A, Al-Marzooq Farah
Department of Microbiology, College of Medicine, University of Anbar, Ramadi, Anbar Governorate, Iraq.
Department of Microbiology and Immunology, College of Medicine and Health Sciences, United Arab Emirates University, Al-Ain, United Arab Emirates.
Front Cell Infect Microbiol. 2025 May 30;15:1588446. doi: 10.3389/fcimb.2025.1588446. eCollection 2025.
Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) technology has emerged as an adaptable instrument for several uses. The CRISPR-Cas system employs Cas proteins and programmable RNA molecules to guide the recognition and cleavage of specific DNA regions, permitting accurate genome editing. It is derived from the bacterial immune system and allows for accurate and efficient modification of DNA sequences. This technique provides unparalleled gene editing, control, and precise alteration opportunities. This review aims to offer a comprehensive update of the core concepts of the CRISPR-Cas system and recent progress, while also providing an overview of the significant applications in diverse fields such as microbiology and medicine. The CRISPR-Cas9 gene editing technique has facilitated substantial advancements in comprehending gene function, simulating diseases, and creating innovative therapeutics. CRISPR-based therapeutics present a hopeful prospect for addressing intricate ailments, including genetic disorders, malignancies, and infectious diseases, as they serve as viable substitutes for conventional pharmaceuticals. In microbiology, this method serves as a diagnostic and therapeutic tool that proves highly efficient in eliminating bacteria that have developed resistance to various antibiotics. Despite its significant potential, CRISPR encounters ethical, safety, and regulatory obstacles that necessitate meticulous deliberation. Concerns regarding off-target effects, poor delivery to target tissues, and unwanted side effects emphasize the necessity to thoroughly examine the technology. It is necessary to balance the advantages and difficulties CRISPR presents. Consequently, more rigorous preclinical and clinical experiments are essential before using it in humans.
成簇规律间隔短回文重复序列(CRISPR)技术已成为一种适用于多种用途的工具。CRISPR-Cas系统利用Cas蛋白和可编程RNA分子来引导对特定DNA区域的识别和切割,从而实现精确的基因组编辑。它源自细菌免疫系统,能够对DNA序列进行准确而高效的修饰。这项技术提供了无与伦比的基因编辑、调控和精确改变的机会。本综述旨在全面更新CRISPR-Cas系统的核心概念和最新进展,同时概述其在微生物学和医学等不同领域的重要应用。CRISPR-Cas9基因编辑技术在理解基因功能、模拟疾病和开发创新疗法方面取得了重大进展。基于CRISPR的疗法为解决包括遗传疾病、恶性肿瘤和传染病在内的复杂疾病带来了充满希望的前景,因为它们可作为传统药物的可行替代品。在微生物学中,这种方法可作为一种诊断和治疗工具,在消除对各种抗生素产生耐药性的细菌方面被证明非常有效。尽管CRISPR具有巨大潜力,但它也面临着伦理、安全和监管方面的障碍,需要仔细考虑。对脱靶效应、向靶组织递送不佳以及不良副作用的担忧凸显了全面审查该技术的必要性。有必要权衡CRISPR带来的优势和困难。因此,在将其用于人类之前,进行更严格的临床前和临床试验至关重要。