抗生素
骨水泥
金黄色葡萄球菌
微生物学
骨感染
细菌
葡萄球菌感染
葡萄球菌
医学
植入
牙科
生物
水泥
材料科学
外科
冶金
遗传学
作者
Sumana Ghosh,M. Sinha,R. Samanta,Suresh Sadhasivam,Anamika Bhattacharyya,Ashis Nandy,Swamini Saini,Nupur Tandon,Himanshi Singh,Swati Gupta,Anjali Chauhan,Keerthi Kumar Aavula,Sneha Susan Varghese,Pujie Shi,Sudip Kumar Ghosh,Mukesh Garg,Tanmoy Saha,Aparna Padhye,S. Ghosh,Hae Lin Jang,Shiladitya Sengupta
标识
DOI:10.1038/s41551-022-00950-x
摘要
New antibiotics should ideally exhibit activity against drug-resistant bacteria, delay the development of bacterial resistance to them and be suitable for local delivery at desired sites of infection. Here, we report the rational design, via molecular-docking simulations, of a library of 17 candidate antibiotics against bone infection by wild-type and mutated bacterial targets. We screened this library for activity against multidrug-resistant clinical isolates and identified an antibiotic that exhibits potent activity against resistant strains and the formation of biofilms, decreases the chances of bacterial resistance and is compatible with local delivery via a bone-cement matrix. The antibiotic-loaded bone cement exhibited greater efficacy than currently used antibiotic-loaded bone cements against staphylococcal bone infections in rats. Potent and locally delivered antibiotic-eluting polymers may help address antimicrobial resistance. An antibiotic identified via molecular-docking simulations and screening, and loaded into a bone-cement matrix, performs better than currently used antibiotic-loaded bone cements in the treatment of staphylococcal bone infections in rats.
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