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阿米卡星与亚胺培南联合用药对多重耐药菌的体外和体内效应

In Vitro and In Vivo Effect of Amikacin and Imipenem Combinations against Multidrug-Resistant .

作者信息

Farhan Sara Mahmoud, El-Baky Rehab Mahmoud Abd, Abdalla Salah, El-Gendy Ahmed Osama, Ahmed Hala Rady, Mohamed Doaa Safwat, El Zawily Amr, Azmy Ahmed Farag

机构信息

Department of Microbiology and Immunology, Faculty of Pharmacy, Beni-Suef University, Beni-Suef 62514, Egypt 2 Department of Microbiology and Immunology, Faculty of Pharmacy, Deraya University, Minia 11566, Egypt 3 Department of Microbiology and Immunology, Faculty of Pharmacy, Minia University, Minia 61519, Egypt 4 Department of Microbiology and Immunology, Faculty of Pharmacy, Suez Canal University, Ismailia 41522, Egypt 5 Department of Microbiology and Immunology, Faculty of Pharmacy, Sohag University, Sohag 82524, Egypt 6 Department of Plant and Microbiology, Faculty of Science, Damanhour University, Damanhour 22511, Egypt 7 Department of Pharmaceutical Sciences and Experimental Therapeutics, College of Pharmacy, University of Iowa, Iowa City, IA 52242, USA.

Department of Microbiology and Immunology, Faculty of Pharmacy, Deraya University, Minia 11566, Egypt.

出版信息

Trop Med Infect Dis. 2022 Oct 2;7(10):281. doi: 10.3390/tropicalmed7100281.

Abstract

The emergence of multidrug-resistant (MDR) has developed worldwide; therefore, the use of antibiotic combinations may be an effective strategy to target resistant bacteria and fight life-threatening infections. The current study was performed to evaluate the in vitro and in vivo efficacy of amikacin and imipenem alone and in combination against multidrug-resistant Methods: The combination treatment was assessed in vitro using a checkerboard technique and time-killing curve and in vivo using a peritonitis mouse model. In resistant isolates, conventional PCR and quantitative real-time PCR techniques were used to detect the resistant genes of Metallo-β-lactamase gene Imipenemase () and aminoglycoside 6'-N-acetyltransferase (aac ). Scanning electron microscopy was used to detect the morphological changes in the resistant isolates after treatment with each drug alone and in combination. In vitro and in vivo studies showed a synergistic effect using the tested antibiotic combinations, showing fractional inhibitory concentration indices (FICIs) of ≤0.5. Regarding the in vivo study, combination therapy indicated a bactericidal effect after 24 h. isolates harboring the resistant genes Metallo-β-lactamase gene Imipenemase () and aminoglycoside 6'-N-acetyltransferase () represented 80% and 66.7%, respectively, which were mainly isolated from wound infections. The lowest effect on Metallo-β-lactamase gene Imipenemase () and aminoglycoside 6'-N-acetyltransferase () gene expression was shown in the presence of 0.25 × MIC of imipenem and 0.5 × MIC of amikacin. The scanning electron microscopy showed cell shrinkage and disruption in the outer membrane of in the presence of the antibiotic combination. Amikacin and imipenem combination can be expected to be effective in the treatment and control of serious infections caused by multidrug-resistant (MDR) and the reduction in bacterial resistance emergence.

摘要

多重耐药(MDR)现象已在全球范围内出现;因此,使用抗生素联合疗法可能是针对耐药菌并对抗危及生命感染的有效策略。本研究旨在评估阿米卡星和亚胺培南单独及联合使用对多重耐药菌的体外和体内疗效。方法:采用棋盘法和时间杀菌曲线在体外评估联合治疗效果,并使用腹膜炎小鼠模型在体内进行评估。对于耐药菌株,使用常规PCR和定量实时PCR技术检测金属β-内酰胺酶基因亚胺培南酶()和氨基糖苷6'-N-乙酰转移酶(aac)的耐药基因。使用扫描电子显微镜检测单独及联合使用每种药物处理后耐药菌株的形态变化。体外和体内研究表明,所测试的抗生素联合使用具有协同作用,部分抑菌浓度指数(FICIs)≤0.5。关于体内研究,联合治疗在24小时后显示出杀菌效果。携带金属β-内酰胺酶基因亚胺培南酶()和氨基糖苷6'-N-乙酰转移酶()耐药基因的菌株分别占80%和66.7%,主要从伤口感染中分离得到。在亚胺培南0.25×MIC和阿米卡星0.5×MIC存在的情况下,对金属β-内酰胺酶基因亚胺培南酶()和氨基糖苷6'-N-乙酰转移酶()基因表达的影响最小。扫描电子显微镜显示,在抗生素联合使用的情况下,细胞出现收缩和外膜破裂。预计阿米卡星和亚胺培南联合使用对治疗和控制多重耐药(MDR)引起的严重感染以及减少细菌耐药性的出现有效。

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