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Improving predictions of the risk of resistance development against new and old antibiotics

机译:对新旧抗生素产生耐药性风险的预测得到改善

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The methods used today by academic researchers and the pharmaceutical industry to assess the risk of emergence of resistance, for example during development of new antibiotics or when assessing an old antibiotic, are sub-optimal. Even though easy to perform, the presently used serial passage procedures, minimal prevention concentration measurements and determination of mutation rates in vitro are generally providing inadequate knowledge for risk assessment and making decisions to continue/discontinue drug development. These methods need to be complemented and replaced with more relevant methods such as determination of whether resistance genes already pre-exist in various metagenomes, and the likelihood that these genes can transfer into the relevant pathogens and be stably maintained. Furthermore, to determine the risk of emergence of mutationally conferred resistance the fitness effect of the resistance mechanism is key, as this parameter will determine the ability of the resistant mutants to be maintained and enriched in the host after they have emerged. This information combined with knowledge of bacterial population sizes and growth and killing dynamics at relevant infection sites should allow for better forecasting of the risk of resistance emerging in clinical settings. Clinical Microbiology and Infection (C) 2015 European Society of Clinical Microbiology and Infectious Diseases. Published by Elsevier Ltd. All rights reserved.
机译:目前,学术研究人员和制药行业用于评估耐药性出现风险的方法(例如在开发新抗生素过程中或评估旧抗生素时)并不理想。尽管易于执行,但目前使用的连续传代程序,最小的预防浓度测量和体外突变率的测定通常无法提供足够的知识来进行风险评估以及做出继续/终止药物开发的决定。这些方法需要补充并用更相关的方法代替,例如确定抗性基因是否已在各种元基因组中预先存在,以及确定这些基因能否转移到相关病原体中并得到稳定维持的可能性。此外,为了确定产生突变赋予的抗性的风险,抗性机制的适应性作用是关键,因为该参数将确定抗性突变体出现后在宿主中维持和富集的能力。该信息与细菌种群数量和生长以及相关感染部位的杀灭动态的知识相结合,应该可以更好地预测临床环境中出现耐药性的风险。临床微生物学和感染(C)2015年欧洲临床微生物学和传染病学会。由Elsevier Ltd.出版。保留所有权利。

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