Araujo Bruna Fuga, Ferreira Melina Lorraine, Campos Paola Amaral de, Royer Sabrina, Batistão Deivid William da Fonseca, Dantas Raquel Cristina Cavalcanti, Gonçalves Iara Rossi, Faria Ana Luiza Souza, Brito Cristiane Silveira de, Yokosawa Jonny, Gontijo-Filho Paulo Pinto, Ribas Rosineide Marques
Instituto de Ciências Biomédicas (ICBIM), Laboratory of Molecular Microbiology, Universidade Federal de Uberlandia (UFU), Uberlandia, Minas Gerais, Brazil.
Instituto de Ciências Biomédicas (ICBIM), Laboratory of Virology, Universidade Federal de Uberlandia (UFU), Uberlandia, Minas Gerais, Brazil.
PLoS One. 2016 May 24;11(5):e0155914. doi: 10.1371/journal.pone.0155914. eCollection 2016.
We described a comprehensive analysis of the molecular epidemiology of multidrug-resistant (MDR) P. aeruginosa. Molecular analysis included typing by Pulsed Field Gel Electrophoresis, identification of genes of interest through PCR-based assays and sequencing of target genes. Case-control study was conducted to better understand the prognostic of patients and the impact of inappropriate therapy in patients with bacteremia, as well as the risk factors of MDR infections. We observed a high rate of MDR isolates (40.7%), and 51.0% of them was independently associated with inappropriate antibiotic therapy. Bacteremia was detected in 66.9% of patients, and prolonged hospital stay was expressive in those resistant to fluoroquinolone. Plasmid-mediated quinolone resistance genes (PMQR), qnrS1 and aac(6')Ib-cr, were detected in two different nosocomial isolates (5.3%), and the aac(6')-Ib7 variant was detected at a high frequency (87.5%) in those negative to PMQR. The presence of mutations in gyrA and parC genes was observed in 100% and 85% of selected isolates, respectively. Isolates harboring PMQR genes or mutations in gyrA and parC were not closely related, except in those containing SPM (São Paulo metallo-β-lactamase) clone. In addition, there is no study published in Brazil to date reporting the presence of Pseudomonas aeruginosa isolates harboring both qnrS1 and aac(6')Ib-cr genes, with alarming frequency of patients with inappropriate therapy.
我们描述了对多重耐药铜绿假单胞菌分子流行病学的全面分析。分子分析包括脉冲场凝胶电泳分型、通过基于聚合酶链反应的检测鉴定感兴趣的基因以及对目标基因进行测序。开展病例对照研究以更好地了解患者的预后、不恰当治疗对菌血症患者的影响以及多重耐药感染的危险因素。我们观察到多重耐药菌株的比例很高(40.7%),其中51.0%与不恰当的抗生素治疗独立相关。66.9%的患者检测到菌血症,对氟喹诺酮耐药的患者住院时间延长情况明显。在两种不同的医院分离株(5.3%)中检测到质粒介导的喹诺酮耐药基因(PMQR)、qnrS1和aac(6')Ib-cr,在对PMQR呈阴性的分离株中,aac(6')-Ib7变体的检测频率很高(87.5%)。分别在100%和85%的选定分离株中观察到gyrA和parC基因存在突变。携带PMQR基因或gyrA和parC基因突变的分离株除了含有圣保罗金属β-内酰胺酶(SPM)克隆的那些外,没有密切关系。此外,迄今为止巴西没有发表的研究报告同时携带qnrS1和aac(6')Ib-cr基因的铜绿假单胞菌分离株的存在情况,以及不恰当治疗患者的惊人频率。