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首页> 外文期刊>Annals of microbiology >Synergistic effect of polyethylenimine plus piperacillin/tazobactam on clinicalPseudomonas aeruginosa isolates resistant to piperacillin/tazobactam
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Synergistic effect of polyethylenimine plus piperacillin/tazobactam on clinicalPseudomonas aeruginosa isolates resistant to piperacillin/tazobactam

机译:聚乙烯亚胺加哌拉西林/他唑巴坦对临床耐药的铜绿假单胞菌铜绿假单胞菌/他唑巴坦的协同作用

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We investigated thein vitro susceptibility of piperacillin/tazobactam in association with polyethylenimine (PEI), a synthetic polycation polymer, against 24 clinical isolates ofPsedomonas aeruginosa resistant to piperacillin/tazobactam. The strains were isolated from patients with respiratory tract infections. MIC of piperacillin/tazobactam was determined by agar dilution method in accordance with NCCLS methodology. An inoculum of 104 CFU/spot with or without PEI (250 nM final concentration) was used. Killing curves were performed for 3 piperacillin/tazobactam resistant strains chosen for their different range of MIC values to piperacillin/tazobactam (128, 256 and 512 mg/L, respectively). Analyses were performed in duplicate using a concentration of antibiotic of 16 mg/L. The addition of PEI (250 nM) increased the susceptibility of piperacillin/tazobactam (from 8 to 32 folds) in all the strains tested. Moreover, in all the strains tested piperacillin/tazobactam in association with PEI showed a bactericidal activity before 6 h. Intrinsic resistance ofP. aeruginosa affects susceptibility to penicillins and is believed to entail broad spectrum impermeability. Different theories suggest that some degree of structure or organization exists in the periplasm ofP. aeruginosa and that this modulates both the level of intrinsic, impermeability-determined resistance expressed by a strain and the efficiency with which the β-lactamase can contact and destroy the incoming β-lactamase molecules. The explanation of this behaviour could be that PEI determines an increased permeability of the outer membrane ofP. aeruginosa; tazobactam inhibits β-lactamase allowing the antibacterial activity of piperacillin. In conclusion our data suggest that PEI can be expected to act as a vehicle for experimental drug delivery into cells, and as a potentiating agent for antibacterial agents that are normally excluded by Gram-negative bacteria.
机译:我们调查了哌拉西林/他唑巴坦联合聚乙烯亚胺(PEI),一种合成的聚阳离子聚合物,对铜绿假单胞菌对哌拉西林/他唑巴坦耐药的24种临床分离株的体外敏感性。从呼吸道感染患者中分离出菌株。根据NCCLS方法,通过琼脂稀释法测定哌拉西林/他唑巴坦的MIC。使用104 CFU /点的接种物,有或没有PEI(终浓度250 nM)。针对3种对哌拉西林/他唑巴坦具有抗性的菌株进行了杀伤曲线,这些菌株的MIC值与哌拉西林/他唑巴坦的MIC范围不同(分别为128、256和512 mg / L)。使用16 mg / L的抗生素浓度进行一式两份的分析。在所有测试的菌株中,PEI(250 nM)的添加增加了哌拉西林/他唑巴坦的敏感性(从8倍增加到32倍)。此外,在所有测试的菌株中,哌拉西林/他唑巴坦与PEI的结合在6 h前显示出杀菌活性。 P的固有抗性。铜绿菌影响对青霉素的敏感性,并被认为具有广谱不渗透性。不同的理论表明P的周质中存在某种程度的结构或组织。铜绿假单胞菌,这既调节了由菌株表达的内在的,不渗透性确定的抗性水平,又调节了β-内酰胺酶可以接触和破坏进入的β-内酰胺酶分子的效率。此行为的解释可能是PEI决定了P外膜的渗透性增加。铜绿他唑巴坦抑制β-内酰胺酶,从而使哌拉西林具有抗菌活性。总之,我们的数据表明,PEI有望充当将实验药物传递到细胞中的媒介,并成为通常被革兰氏阴性细菌所排除的抗菌剂的增强剂。

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