非抗菌药物:依托度酸作为抗ESKAPE病原体的可能的抗菌或佐剂。

Q3 Immunology and Microbiology Open Microbiology Journal Pub Date : 2018-08-31 eCollection Date: 2018-01-01 DOI:10.2174/1874285801812010288
Sónia G Pereira, Vanessa S Domingues, João Theriága, Maria de Jesus Chasqueira, Paulo Paixão
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引用次数: 12

摘要

多重耐药细菌在卫生保健单位呈指数级增长,威胁公共卫生,需要新的治疗方法。2017年,世界卫生组织发布了一份清单,将耐药细菌列为研究抗药新药的优先级别。方法与材料:耐药ESKAPE(粪肠球菌、金黄色葡萄球菌、肺炎克雷伯菌、鲍曼不动杆菌、铜绿假单胞菌、肠杆菌等)和粪肠球菌、大肠杆菌等病原体均在本清单中。采用肉汤微量稀释技术,对各菌株的代表性分离物在10和1 mM条件下的抑菌和抗生物膜形成活性进行了测试。结果与讨论:所有检测的革兰氏阳性结果均有统计学意义(p< 0.05),特别是对粪肠杆菌的抗生物膜活性。除了一种鲍曼不动杆菌临床分离物对生物膜形成的抑制作用外,依托度酸对测试的革兰氏阴性菌几乎没有影响。观察到的差异值得进一步分析和展望所涉及的机制,以揭示可能用于药物开发的新细菌靶点。与其他非甾体抗炎药类似的工作也值得探索,以确定这些药物的新治疗应用,特别是在生物膜形成抑制方面,或作为当前抗生素治疗的佐剂,主要针对革兰氏阳性,正如目前的工作所建议的那样。结论:已经批准的药物在药代动力学和安全性方面可能为针对重点病原体的抗菌治疗提供更快的解决方案。目前的工作旨在引起人们对这种可能性的关注,特别是在非甾体抗炎药、抗生物膜形成和最优先的病原体方面。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Non-Antimicrobial Drugs: Etodolac as a Possible Antimicrobial or Adjuvant Agent Against ESKAPE Pathogens.

Introduction: Multiple-drug resistant bacteria are emerging exponentially in healthcare units, threatening public health and requiring novel therapeutic approaches. In 2017, World Health Organization published a list that frames antimicrobial resistant bacteria into priority levels for research of novel drugs to fight them.

Methods & materials: Antimicrobial resistant ESKAPE (Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, Enterobacter sp.) and Enterococcus faecalis and Escherichia coli pathogens are present in this list. Representative isolates of each species were used to test the Antibacterial and anti-biofilm formation activities of Etodolac (a Non-Steroidal Anti-Inflammatory Drug, NSAID) at 10 and 1 mM using a broth microdilution technique.

Results & discussion: Statistically significant (p< 0,05) results were observed against all tested gram-positives, particularly anti-biofilm activity against E. faecium. Etodolac had an almost null influence on tested gram-negatives, with the exception of one A. baumannii clinical isolate regarding biofilm formation inhibition. Observed differences deserve further analysis and prospection of the involved mechanisms, to unravel possible novel bacterial targets for drug development. Similar work with other NSAID's may also be worth exploring to ascertain novel therapeutic applications for these drugs, particularly regarding biofilm formation inhibition, per si or as adjuvants of current antibiotherapy, mainly against gram-positives, as suggested by present work.

Conclusion: Already approved drugs in terms of pharmacokinetics and safety may deploy faster solutions for antimicrobial therapy against priority pathogens. Current work intends to bring attention to that possibility, particularly regarding NSAIDs, anti-biofilm formation and top priority pathogens.

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来源期刊
Open Microbiology Journal
Open Microbiology Journal Immunology and Microbiology-Immunology and Microbiology (all)
CiteScore
1.80
自引率
0.00%
发文量
24
期刊介绍: The Open Microbiology Journal is a peer-reviewed open access journal which publishes research articles, reviews/mini-reviews, case studies, guest edited thematic issues and short communications/letters covering theoretical and practical aspects of Microbial systematics, evolutionary microbiology, immunology, virology, parasitology , bacteriology, mycology, phycology, protozoology, microbial ecology, molecular biology, microbial physiology, biochemistry, microbial pathogenesis, host-microbe interaction, systems microbiology, synthetic microbiology, bioinformatics. The Open Microbiology Journal , a peer-reviewed journal, is an important and reliable source of current information on developments in the field. The emphasis will be on publishing quality papers rapidly and freely available to researchers worldwide.
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