Navidifar Tahereh, Amin Mansour, Rashno Mohammad
Cellular and Molecular Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Department of Microbiology, School of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Infect Drug Resist. 2019 May 7;12:1099-1111. doi: 10.2147/IDR.S199993. eCollection 2019.
Sub-minimal inhibitory concentrations of antibiotics have been indicated to affect the biofilm formation in pathogens of nosocomial infections. This study aimed to investigate the effects of meropenem and tigecycline at their sub-minimum inhibitory concentrations (MICs) on the biofilm formation capacity of (, as well as the expression levels of genes involved in biofilm formation, quorum sensing, pili assembly and efflux pumps. In this study, four non-clonal strains (AB10, AB13, AB32 and AB55), which were different from the aspects of antibiotic susceptibility and biofilm formation from each other were selected for the evaluation of antimicrobial susceptibility, biofilm inducibility at sub-MICs of meropenem and tigecycline and the gene expression levels (the genes). A significant increase in the MICs of all antibiotics was demonstrated in the biofilm cells in each four strains. The biofilm formation was significantly decreased in all the representative strains exposed to tigecycline. However, the biofilm inducibility at sub-MICs of meropenem was dependent on strain genotype. In concordance with these results, Pearson correlation analysis indicated a positive significant correlation between the biofilm formation capacity and the mRNA levels of genes encoding efflux pumps except , the genes involved in biofilm formation, pili assembly and quorum sensing following exposure to meropenem and tigecycline at their sub-MICs. These results revealed valuable data into the correlation between the gene transcription levels and biofilm formation, as well as quorum sensing and their regulation at sub-MICs of meropenem and tigecycline.
已表明抗生素的亚最小抑菌浓度会影响医院感染病原体中的生物膜形成。本研究旨在调查美罗培南和替加环素在其亚最小抑菌浓度(MIC)下对[具体病原体未给出]生物膜形成能力的影响,以及参与生物膜形成、群体感应、菌毛组装和外排泵的基因表达水平。在本研究中,选择了四株非克隆菌株(AB10、AB13、AB32和AB55),它们在抗生素敏感性和生物膜形成方面彼此不同,用于评估抗菌药敏性、美罗培南和替加环素亚MIC下的生物膜诱导性以及基因表达水平([具体基因未给出]基因)。在每四株菌株的生物膜细胞中,所有抗生素的MIC均显著增加。在所有暴露于替加环素的代表性菌株中,生物膜形成显著减少。然而,美罗培南亚MIC下的生物膜诱导性取决于菌株基因型。与这些结果一致,Pearson相关性分析表明,在亚MIC下暴露于美罗培南和替加环素后,生物膜形成能力与编码外排泵的基因、参与生物膜形成、菌毛组装和群体感应的基因的mRNA水平之间存在显著正相关。这些结果揭示了关于美罗培南和替加环素亚MIC下基因转录水平与生物膜形成以及群体感应及其调控之间相关性的有价值数据。