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首页> 外文期刊>International journal of antimicrobial agents >In vitro reduction of antibacterial activity of tigecycline against multidrug-resistant Acinetobacter baumannii with host stress hormone norepinephrine
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In vitro reduction of antibacterial activity of tigecycline against multidrug-resistant Acinetobacter baumannii with host stress hormone norepinephrine

机译:宿主应激激素去甲肾上腺素体外降低替加环素对多重耐药鲍曼不动杆菌的抗菌活性

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The host stress hormone norepinephrine (NE), also called noradrenaline, is reported to augment bacterial growth and pathogenicity, but few studies have focused on the effect of NE on the activity of antimicrobials. The aim of this study was to clarify whether NE affects antimicrobial activity against multidrug-resistant Acinetobacter baumannii (MDR-AB). Time-kill studies of tigecycline (TIG) and colistin (COL) against MDR-AB as well as assays for factors contributing to antibiotic resistance were performed using MDR-AB clinical strains both in the presence and absence of 10 mu M NE. In addition, expression of three efflux pump genes (adeB, adeJ and adeG) in the presence and absence of NE was analysed by quantitative reverse transcription PCR. Viable bacterial cell counts in TIG-supplemented medium containing NE were significantly increased compared with those in medium without NE. In contrast, NE had little influence on viable bacterial cell counts in the presence of COL. NE-supplemented medium resulted in an ca. 2 log increase in growth and in bacterial cell numbers adhering on polyurethane, silicone and polyvinylchloride surfaces. Amounts of biofilm in the presence of NE were ca. 3-fold higher than without NE. Expression of the adeG gene was upregulated 4-6-fold in the presence of NE. In conclusion, NE augmented factors contributing to antibiotic resistance and markedly reduced the in vitro antibacterial activity of TIG against MDR-AB. These findings suggest that NE treatment may contribute to the failure of TIG therapy in patients with MDR-AB infections. (C) 2016 Elsevier B.V. and International Society of Chemotherapy. All rights reserved.
机译:据报道,宿主应激激素去甲肾上腺素(NE)也称为去甲肾上腺素,可增强细菌的生长和致病性,但很少有研究集中于NE对抗菌活性的影响。这项研究的目的是澄清NE是否影响对多重耐药的鲍曼不动杆菌(MDR-AB)的抗菌活性。在存在和不存在10μMNE的情况下,均使用MDR-AB临床菌株进行了替加环素(TIG)和大肠菌素(COL)对抗MDR-AB的时间杀灭研究以及对导致抗生素耐药性的因素的测定。另外,通过定量逆转录PCR分析存在和不存在NE时三个外排泵基因(adeB,adeJ和adeG)的表达。与不含NE的培养基相比,含NE的TIG培养基中的活细菌细胞计数显着增加。相反,在存在COL的情况下,NE对活细菌细胞计数的影响很小。添加NE的培养基导致ca.附着在聚氨酯,有机硅和聚氯乙烯表面上的细菌和细菌的生长数量增加了2 log。 NE存在下生物膜的量约为。比无NE高3倍。在NE存在下,adeG基因的表达被上调了4-6倍。总之,NE增强了导致抗生素耐药性的因子,并显着降低了TIG对MDR-AB的体外抗菌活性。这些发现表明,NE治疗可能会导致MDR-AB感染患者的TIG治疗失败。 (C)2016 Elsevier B.V.和国际化学疗法学会。版权所有。

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