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荧光大环内酯类探针——合成及其在细菌耐药性评估中的应用

Fluorescent macrolide probes - synthesis and use in evaluation of bacterial resistance.

作者信息

Stone M Rhia L, Łapińska Urszula, Pagliara Stefano, Masi Muriel, Blanchfield Joanne T, Cooper Matthew A, Blaskovich Mark A T

机构信息

Centre for Superbug Solutions, Institute for Molecular Bioscience, The University of Queensland 306 Carmody Road St Lucia 4072 Brisbane Australia

Living Systems Institute, University of Exeter Exeter EX4 4QD UK.

出版信息

RSC Chem Biol. 2020 Nov 17;1(5):395-404. doi: 10.1039/d0cb00118j. eCollection 2020 Dec 1.

Abstract

The emerging crisis of antibiotic resistance requires a multi-pronged approach in order to avert the onset of a post-antibiotic age. Studies of antibiotic uptake and localisation in live cells may inform the design of improved drugs and help develop a better understanding of bacterial resistance and persistence. To facilitate this research, we have synthesised fluorescent derivatives of the macrolide antibiotic erythromycin. These analogues exhibit a similar spectrum of antibiotic activity to the parent drug and are capable of labelling both Gram-positive and -negative bacteria for microscopy. The probes localise intracellularly, with uptake in Gram-negative bacteria dependent on the level of efflux pump activity. A plate-based assay established to quantify bacterial labelling and localisation demonstrated that the probes were taken up by both susceptible and resistant bacteria. Significant intra-strain and -species differences were observed in these preliminary studies. In order to examine uptake in real-time, the probe was used in single-cell microfluidic microscopy, revealing previously unseen heterogeneity of uptake in populations of susceptible bacteria. These studies illustrate the potential of fluorescent macrolide probes to characterise and explore drug uptake and efflux in bacteria.

摘要

抗生素耐药性这一新兴危机需要采取多管齐下的方法,以避免进入后抗生素时代。对活细胞中抗生素摄取和定位的研究可能会为改进药物的设计提供信息,并有助于更好地理解细菌的耐药性和持续性。为了推动这项研究,我们合成了大环内酯类抗生素红霉素的荧光衍生物。这些类似物展现出与母体药物相似的抗生素活性谱,并且能够对革兰氏阳性菌和革兰氏阴性菌进行标记以便于显微镜观察。这些探针定位于细胞内,在革兰氏阴性菌中的摄取取决于外排泵活性水平。建立了一种基于平板的测定法来量化细菌标记和定位,结果表明这些探针可被敏感菌和耐药菌摄取。在这些初步研究中观察到了显著的菌株内和种间差异。为了实时检测摄取情况,该探针被用于单细胞微流控显微镜观察,揭示了敏感菌群体中以前未被发现的摄取异质性。这些研究说明了荧光大环内酯探针在表征和探索细菌中药物摄取及外排方面的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4695/8341779/225712e8fdfe/d0cb00118j-f1.jpg

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