Founder & CEO at Times of Biotech, Navelim Bicholim, Goa-403505, India.
Microbiology, Fermentation & Biotechnology Division, ICAR- Central Institute of Fisheries Technology, Cochin-29, Kerala, India.
Funct Integr Genomics. 2024 May 28;24(3):110. doi: 10.1007/s10142-024-01362-7.
With the growing population, demand for food has dramatically increased, and fisheries, including aquaculture, are expected to play an essential role in sustaining demand with adequate quantities of protein and essential vitamin supplements, employment generation, and GDP growth. Unfortunately, the incidence of emerging/re-emerging AMR pathogens annually occurs because of anthropogenic activities and the frequent use of antibiotics in aquaculture. These AMR pathogens include the WHO's top 6 prioritized ESKAPE pathogens (nosocomial pathogens: Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, and Enterobacter spp.), extended-spectrum beta lactases (ESBLs) and carbapenemase-producing E. coli, which pose major challenges to the biomagnification of both nonnative and native antibiotic-resistant bacteria in capture and cultured fishes. Although implementing the rational use of antibiotics represents a promising mitigation measure, this approach is practically impossible due to the lack of awareness among farmers about the interplay between antimicrobial use and the emergence of antimicrobial resistance (AMR). Nevertheless, to eradicate these 'superbugs,' CRISPR/Cas (clustered regularly interspersed short palindromic repeats/CRISPR associate protein) has turned out to be a novel approach owing to its ability to perform precise site-directed targeting/knockdown/reversal of specific antimicrobial resistance genes in vitro and to distinguish AMR-resistant bacteria from a plethora of commensal aquatic bacteria. Along with highlighting the importance of virulent multidrug resistance genes in bacteria, this article aims to provide a holistic picture of CRISPR/Cas9-mediated genome editing for combating antimicrobial-resistant bacteria isolated from various aquaculture and marine systems, as well as insights into different types of CRISPR/Cas systems, delivery methods, and challenges associated with developing CRISPR/Cas9 antimicrobial agents.
随着人口的增长,对食物的需求大幅增加,预计渔业(包括水产养殖)将在维持足够数量的蛋白质和必需维生素补充剂、创造就业机会和 GDP 增长方面发挥重要作用。不幸的是,由于人为活动和水产养殖中抗生素的频繁使用,每年都会出现新出现/重新出现的 AMR 病原体。这些 AMR 病原体包括世卫组织优先考虑的 6 种 ESKAPE 病原体(医院病原体:屎肠球菌、金黄色葡萄球菌、肺炎克雷伯菌、鲍曼不动杆菌、铜绿假单胞菌和肠杆菌属)、产超广谱β-内酰胺酶(ESBL)和产碳青霉烯酶的大肠杆菌,这对捕获和养殖鱼类中非本地和本地抗生素耐药细菌的生物放大构成了重大挑战。尽管实施抗生素的合理使用代表了一种有前途的缓解措施,但由于农民缺乏对抗生素使用与抗生素耐药性(AMR)出现之间相互作用的认识,这种方法实际上是不可能的。然而,为了消灭这些“超级细菌”,CRISPR/Cas(成簇规律间隔短回文重复/CRISPR 相关蛋白)已被证明是一种新方法,因为它能够在体外对特定抗生素耐药基因进行精确的靶向/敲低/逆转,并将 AMR 耐药细菌与大量共生水生细菌区分开来。本文除了强调细菌中有毒的多药耐药基因的重要性外,还旨在提供一种综合的方法,用于对抗从各种水产养殖和海洋系统中分离出的抗微生物耐药细菌的 CRISPR/Cas9 介导的基因组编辑,以及深入了解不同类型的 CRISPR/Cas 系统、传递方法以及与开发 CRISPR/Cas9 抗菌剂相关的挑战。