Fonseca A P, Extremina C, Fonseca A F, Sousa J C
Department of Microbiology, Faculty of Medicine, University of Porto, Portugal 2IPATIMUP - Institute of Molecular Pathology and Immunology, University of Porto, Portugal 3Department of Microbiology, Faculty of Pharmacy, University of Porto, Portugal.
J Med Microbiol. 2004 Sep;53(Pt 9):903-910. doi: 10.1099/jmm.0.45637-0.
Subinhibitory concentrations (sub-MICs) of antibiotics, although not able to kill bacteria, can modify their physico-chemical characteristics and the architecture of their outermost surface and may interfere with some bacterial functions. This study investigated the ability of sub-MIC piperacillin/tazobactam (P/T) to interfere with the bacterial virulence parameters of adhesiveness, cell-surface hydrophobicity, motility, biofilm formation and sensitivity to oxidative stress. Antimicrobial activity against five Pseudomonas aeruginosa clinical isolates, representative of clonal lineages of 96 strains of nosocomial origin, and six control strains (ATCC 27853, PAO1, AK1, MT1562, PT623, PAO1algC) was evaluated in vitro using the NCCLS microdilution method. The effects of sub-MIC on bacterial adhesion and biofilm formation were studied using a modified microtitre plate assay. The relative cell-surface hydrophobicity of P. aeruginosa strains was determined by measuring their ability to adhere to n-hexadecane. P. aeruginosa that had been exposed overnight to P/T and incubated with P/T in the plate were also screened for their ability to swim using flagella and to twitch and for their sensitivity to oxidative stress. The results obtained showed that the impact of sub-MIC P/T on bacterial characteristics was different for the various strains of P. aeruginosa. There was a change in bacterial morphology and hydrophobicity that could explain a significant decrease in adhesion values in all clinical isolates and controls tested, a decrease in biofilm formation, a significant increase in sensitivity to oxidative stress, a significant decrease in flagellum-mediated swimming and a decrease in type IV fimbriae-mediated twitching. The results obtained indicate that sub-MIC P/T interferes with the pathogenic potential of P. aeruginosa.
抗生素的亚抑菌浓度(亚 MIC)虽无法杀死细菌,但可改变其物理化学特性及其最外层表面结构,并可能干扰某些细菌功能。本研究调查了亚 MIC 哌拉西林/他唑巴坦(P/T)干扰细菌黏附性、细胞表面疏水性、运动性、生物膜形成及对氧化应激敏感性等毒力参数的能力。采用 NCCLS 微量稀释法体外评估了对 5 株铜绿假单胞菌临床分离株(代表 96 株医院来源克隆谱系)及 6 株对照菌株(ATCC 27853、PAO1、AK1、MT1562、PT623、PAO1algC)的抗菌活性。使用改良的微量滴定板试验研究了亚 MIC 对细菌黏附和生物膜形成的影响。通过测量铜绿假单胞菌菌株黏附正十六烷的能力来确定其相对细胞表面疏水性。还筛选了过夜暴露于 P/T 并在平板中与 P/T 孵育的铜绿假单胞菌利用鞭毛游动、颤动的能力及其对氧化应激的敏感性。所得结果表明,亚 MIC P/T 对不同铜绿假单胞菌菌株细菌特性的影响各异。细菌形态和疏水性发生了变化,这可以解释在所有测试的临床分离株和对照中黏附值显著降低、生物膜形成减少、对氧化应激的敏感性显著增加、鞭毛介导的游动显著减少以及 IV 型菌毛介导的颤动减少。所得结果表明,亚 MIC P/T 会干扰铜绿假单胞菌的致病潜力。