Cabral Amanda Seabra, Lacerda Fernanda de Freitas, Leite Vitor Luis Macena, de Miranda Filipe Martire, da Silva Amanda Beiral, Dos Santos Bárbara Araújo, Lima Jailton Lobo da Costa, Teixeira Lúcia Martins, Neves Felipe Piedade Gonçalves
Instituto Biomédico, Universidade Federal Fluminense, Alameda Barros Terra, S/N, São Domingos, Niterói, RJ, 24020-150, Brazil.
Instituto de Microbiologia, Universidade Federal Do Rio de Janeiro, Av. Carlos Chagas Filho, 373, Rio de Janeiro, RJ, 21941-590, Brazil.
Braz J Microbiol. 2024 Dec;55(4):3945-3957. doi: 10.1007/s42770-024-01549-x. Epub 2024 Oct 23.
Enterococci are members of the microbiota of humans and other animals. They can also be found in the environment, associated with food, healthcare infections, and hospital settings. Due to their wide distribution, they are inserted in the One Health context. The selective pressure caused by the extensive use of antimicrobial agents in humans, animals, and agriculture has increased the frequency of resistance to various drugs among enterococcal species. CRISPR-Cas system, an important prokaryotic defense mechanism against the entry of mobile genetic elements, may prevent the acquisition of genes involved in antimicrobial resistance and virulence. This system has been increasingly used as a gene editing tool, which can be used as a way to recognize and inactivate genes of interest. Here, we conduct a review on CRISPR systems found in enterococci, considering their occurrence, structure and organization, mechanisms of action and use as a genetic engineering technology. Type II-A CRISPR-Cas systems were shown to be the most frequent among enterococcal species, and the orphan CRISPR2 was the most commonly found system (54.1%) among enterococcal species, especially in Enterococcus faecalis. Distribution of CRISPR systems varied among species. CRISPR systems had 1 to 20 spacers, with size between 23 and 37 bp and direct repeat sequences from 25 to 37 bp. Several applications of the CRISPR-Cas biotechnology have been described in enterococci, mostly in vitro, using this editing tool to target resistance- and virulence-related genes.
肠球菌是人类和其他动物微生物群的成员。它们也存在于环境中,与食物、医疗保健感染及医院环境有关。由于其分布广泛,它们被纳入“同一健康”范畴。在人类、动物和农业中广泛使用抗菌剂所产生的选择压力,增加了肠球菌属物种对各种药物的耐药频率。CRISPR-Cas系统是原核生物抵御移动遗传元件进入的一种重要防御机制,可能会阻止获得与抗菌耐药性和毒力相关的基因。该系统已越来越多地被用作基因编辑工具,可用于识别和使感兴趣的基因失活。在此,我们对肠球菌中发现的CRISPR系统进行综述,考虑它们的出现情况、结构和组织、作用机制以及作为一种基因工程技术的应用。II-A型CRISPR-Cas系统在肠球菌属物种中最为常见,而孤儿CRISPR2是肠球菌属物种中最常发现的系统(54.1%),尤其是在粪肠球菌中。CRISPR系统的分布在不同物种间存在差异。CRISPR系统有1至20个间隔序列,大小在23至37bp之间,直接重复序列为25至37bp。在肠球菌中已描述了CRISPR-Cas生物技术的几种应用,大多是在体外,使用这种编辑工具靶向与耐药性和毒力相关的基因。