Machuca Jesús, Diaz de Alba Paula, Recacha Esther, Pascual Álvaro, Rodriguez-Martinez José Manuel
1 Unidad Intercentros de Enfermedades Infecciosas, Microbiología y Medicina Preventiva, Hospital Universitario Virgen Macarena , Seville, Spain .
2 Institute of Biomedicine of Seville (IBiS) , Seville, Spain .
Microb Drug Resist. 2017 Oct;23(7):822-825. doi: 10.1089/mdr.2016.0245. Epub 2017 Mar 13.
The objective was to evaluate the cytotoxic effect associated with overexpression of multiple Qnr-like plasmid-mediated quinolone resistance (PMQR) mechanisms in Escherichia coli.
Coding regions of different PMQR genes (qnrA1, qnrB1, qnrC, qnrD1, qnrS1, and qepA2) and efsqnr were cloned into pET29a(+) vector and overexpressed in E. coli BL21. E. coli BL21 with and without an empty pET29a(+) vector were used as controls. The cytotoxic effect associated with PMQR mechanism overexpression was determined by transmission electron microscopy and viability assays.
Overexpressed qnr genes produced loss of bacterial viability in the range of 77-97% compared with the controls, comparable with loss of viability associated with EfsQnr overexpression (97%). No loss of viability was observed in E. coli overexpressing QepA2. In transmission electron microscopy assays, signs of cytotoxicity were observed in E. coli cells overexpressing EfsQnr and Qnr proteins (30-45% of the bacterial population showed morphological changes). Morphological changes were observed in less than 5% of bacterial populations from the control strains and E. coli overexpressing QepA2.
Overexpression of qnr genes produces a cytotoxic cellular and structural effect in E. coli, the magnitude of which varies depending on the family of Qnr proteins.
评估与大肠杆菌中多种喹诺酮类耐药基因(Qnr)样质粒介导的喹诺酮耐药机制(PMQR)过表达相关的细胞毒性作用。
将不同PMQR基因(qnrA1、qnrB1、qnrC、qnrD1、qnrS1和qepA2)及efsqnr的编码区克隆至pET29a(+)载体,并在大肠杆菌BL21中过表达。将携带和不携带空pET29a(+)载体的大肠杆菌BL21用作对照。通过透射电子显微镜和活力测定来确定与PMQR机制过表达相关的细胞毒性作用。
与对照相比,过表达的qnr基因导致细菌活力丧失77% - 97%,与EfsQnr过表达导致的活力丧失(97%)相当。过表达QepA2的大肠杆菌未观察到活力丧失。在透射电子显微镜检测中,过表达EfsQnr和Qnr蛋白的大肠杆菌细胞中观察到细胞毒性迹象(30% - 45%的细菌群体显示出形态变化)。对照菌株和过表达QepA2的大肠杆菌中,不到5%的细菌群体观察到形态变化。
qnr基因的过表达在大肠杆菌中产生细胞毒性和结构效应,其程度因Qnr蛋白家族而异。