质粒
清脆的
微生物学
细菌
抗菌剂
生物
细菌接合
抗生素耐药性
基因组编辑
计算生物学
遗传学
基因
作者
Tengfei Long,Shiying Zhou,Zilei Huang,Gong Li,Qin Zhong,Xiaojing Zhang,Yuanyuan Li,Caiping Chen,Lijuan Xia,Ran Wei,Lei Wan,Ang Gao,Hao Ren,Xiaoping Liao,Ya-Hong Liu,Liang Chen,Jian Sun
标识
DOI:10.1021/acssynbio.4c00112
摘要
Antimicrobial resistance poses a significant global challenge, demanding innovative approaches, such as the CRISPR-Cas-mediated resistance plasmid or gene-curing system, to effectively combat this urgent crisis. To enable successful curing of antimicrobial genes or plasmids through CRISPR-Cas technology, the development of an efficient broad-host-range delivery system is paramount. In this study, we have successfully designed and constructed a novel functional gene delivery plasmid, pQ-mini, utilizing the backbone of a broad-host-range Inc.Q plasmid. Moreover, we have integrated the CRISPR-Cas12f system into the pQ-mini plasmid to enable gene-curing in broad-host of bacteria. Our findings demonstrate that pQ-mini facilitates the highly efficient transfer of genetic elements to diverse bacteria, particularly in various species in the order of Enterobacterales, exhibiting a broader host range and superior conjugation efficiency compared to the commonly used pMB1-like plasmid. Notably, pQ-mini effectively delivers the CRISPR-Cas12f system to antimicrobial-resistant strains, resulting in remarkable curing efficiencies for plasmid-borne
科研通智能强力驱动
Strongly Powered by AbleSci AI