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In vitro activity of aztreonam–avibactam against metallo-β-lactamase-producing Enterobacteriaceae—A multicenter study in China

机译:Aztreonam-Avibactam对Metallo-β-内酰胺酶的体外活性,产生生产肠杆菌的多中心研究

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摘要

Objectives: To study the molecular epidemiology of clinical metallo-β-lactamase (MBL)-producing Enterobacteriaceae isolates in China and to evaluate the antimicrobial susceptibility of MBL-Enterobacteriaceae isolates to aztreonam–avibactam. Methods: Bacterial speciation was determined using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. PCR was used to screen for common carbapenemase genes. Antimicrobial susceptibility testing of common clinical antibiotics and aztreonam–avibactam was performed using the standard broth microdilution method. Results: A total of 161 MBL-Enterobacteriaceae isolates were included, with Klebsiella pneumoniae (n = 73, 45.4%) and Escherichia coli (n = 53, 32.9%) being the most common species. Among the 161 isolates, blaNDM (n = 151), blaIMP (n = 13), and blaVIM (n = 2) were detected, including five strains (3.1%) co-harboring two MBLs. MBL-Enterobacteriaceae isolates frequently contained two (n = 55, 34.2%) or more (n = 89, 55.3%) additional serine β-lactamase genes (blaKPC, blaCTX-M, blaTEM, or blaSHV). Antimicrobial susceptibility testing showed that 81.4% of isolates (n = 131) were resistant to aztreonam. The rates of resistance to cefazolin, ceftazidime, ceftriaxone, cefotaxime, ampicillin–sulbactam, amoxicillin–clavulanic acid, and piperacillin–tazobactam were all over 90%. The addition of avibactam (4 μg/ml) significantly reduced the minimum inhibitory concentrations (MICs) of the aztreonam-resistant isolates by more than 8-fold (range ≤0.125 to 4 μg/ml), with a MIC50/MIC90 of ≤0.125/1 μg/ml among the 131 isolates. Overall, 96.9% (n = 156) of the total isolates were inhibited at an aztreonam–avibactam concentration of ≤1 μg/ml. Univariate and multivariate logistic regression analysis found that in patients with MBL-Enterobacteriaceae infections, the presence of pre-existing lung disease (adjusted odds ratio 8.267, 95% confidence interval 1.925–28.297; p = 0.004) was associated with a hazard effect on worse disease outcomes. Conclusions: The combined use of aztreonam–avibactam is highly potent against MBL-Enterobacteriaceae and may serve as a new candidate for the treatment of infections caused by MBL-Enterobacteriaceae in China.
机译:目的:研究临床金属-β-乳酰胺酶(MBL)的分子流行病学 - 施用中国肠杆菌的分离株,评价MBL肠杆菌区分离株与阿兹特瓜兰 - Avibactam的抗微生物敏感性。方法:使用基质辅助激光解吸/电离飞行时间质谱法测定细菌性质。 PCR用于筛选常见的碳结构酶基因。使用标准肉汤微脱离方法进行常见临床抗生素和AztReonam-Avibactam的抗微生物易感性测试。结果:共有161个MBL-exterbacteriaceae分离物,Klebsiella肺炎(n = 73,45.4%)和大肠杆菌(n = 53,32.9%)是最常见的物种。在161个分离物中,检测到共混管(n = 151),Blaimp(n = 13)和Blavim(n = 2),包括五种菌株(3.1%)共同储存两个MBL。 MBL-肠杆菌菌的分离物通常含有两(n = 55,34.2%)或更多(n = 89,55.3%)另外的丝氨酸β-内酰胺酶基因(blakpc,blactx-m,blatem或blashv)。抗微生物易感性测试表明,81.4%的分离株(n = 131)对阿兹特隆耐药。耐含头孢唑啉,头孢他啶,头孢菌,头孢噻肟,氨苄青霉素 - 抑制蛋白,阿莫西林 - 克拉维兰酸和哌啶素 - 塔唑酰胺的率均超过90%。添加紫蛋白(4μg/ mL)的添加显着降低了抗抗抗体分离株的最小抑制浓度(MIC),超过8倍(范围≤0.125至4μg/ ml),MIC50 / MIC90的≤0.125 /1μg/ ml在131分离物中。总体而言,在≤1μg/ ml的AztReonam-Avibactam浓度下抑制了总分离物的96.9%(n = 156)。单变量和多变量逻辑回归分析发现,在患有MBL肠杆菌的患者感染中,存在预先存在的肺病(调整的赔率比8.267,95%置信区间1.925-28.297; p = 0.004)与对更严重的造成影响有关疾病结果。结论:Aztreonam-Avibactam的结合使用对抗MBL-entobacteriaceae具有高度效力,可作为治疗中国MBL-entobacteriaceae引起的感染的新候选者。

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