Brust Flávia Roberta, Boff Luana, da Silva Trentin Danielle, Pedrotti Rozales Franciele, Barth Afonso Luís, Macedo Alexandre José
Faculty of Pharmacy and Center of Biotechnology, Federal University of Rio Grande do Sul, Porto Alegre, Rio Grande do Sul CE 90610-000, Brazil.
Basic Health Sciences Department, Federal University of Health Sciences of Porto Alegre, Porto Alegre, Rio Grande do Sul CE 90050-170, Brazil.
Pathogens. 2019 Apr 14;8(2):49. doi: 10.3390/pathogens8020049.
complex has been increasingly recognized as a nosocomial pathogen representing the third major Enterobacteriaceae species involved with infections. This study aims to evaluate virulence and antimicrobial susceptibility of subpopulations generated from macrocolonies of NDM-1 producing clinical isolates. Biofilm was quantified using crystal violet method and fimbrial genes were investigated by PCR. Susceptibility of antimicrobials, alone and combined, was determined by minimum inhibitory concentration and checkerboard assays, respectively. Virulence and efficacy of antimicrobials were evaluated in larvae. Importantly, we verified that some subpopulations that originate from the same macrocolony present different biofilm production ability and distinct susceptibility to meropenem due to the loss of encoding plasmid. A more in-depth study was performed with the 798 macrocolony subpopulations. Type 3 fimbriae were straightly related with biofilm production; however, virulence in larvae was not statistically different among subpopulations. Triple combination with meropenem-rifampicin-polymyxin B showed in vitro synergistic effect against all subpopulations; while in vivo this treatment showed different efficacy rates for 798-1S and 798-4S subpopulations. The ability of multidrug resistant isolates in generating bacterial subpopulations presenting different susceptible and virulence mechanisms are worrisome and may explain why these infections are hardly overcome.
该菌已日益被视为一种医院病原体,是引发感染的第三大主要肠杆菌科菌种。本研究旨在评估由产NDM-1临床分离株的大菌落产生的亚群的毒力和抗菌敏感性。采用结晶紫法对生物膜进行定量,并通过PCR研究菌毛基因。分别通过最低抑菌浓度和棋盘法测定单独及联合使用抗菌药物的敏感性。在幼虫中评估抗菌药物的毒力和疗效。重要的是,我们证实,由于编码质粒的丢失,一些源自同一大菌落的亚群具有不同的生物膜产生能力和对美罗培南的不同敏感性。对798个大菌落亚群进行了更深入的研究。3型菌毛与生物膜产生直接相关;然而,亚群之间在幼虫中的毒力无统计学差异。美罗培南-利福平-多粘菌素B三联组合对所有亚群均显示出体外协同作用;而在体内,该治疗对798-1S和798-4S亚群显示出不同的有效率。多重耐药分离株产生具有不同敏感和毒力机制的细菌亚群的能力令人担忧,这可能解释了为什么这些感染难以克服。