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使用合成和天然药物联合治疗策略消除 KAPE 病原体生物膜。

Combination drug strategies for biofilm eradication using synthetic and natural agents in KAPE pathogens.

机构信息

Department of Pathology & Microbiology, Breach Candy Hospital Trust, Mumbai, India.

出版信息

Front Cell Infect Microbiol. 2023 Apr 17;13:1155699. doi: 10.3389/fcimb.2023.1155699. eCollection 2023.

Abstract

Antibiotic resistance is a global threat caused by factors such as overuse of antibiotics, lack of awareness, development of biofilms etc. World Health Organization released a list of global priority pathogens which consisted of 12 species of bacteria categorized as expressing critical, high and medium resistance. Several Gram-negative and Gram-positive species are known to cause wide varieties of infections and have become multidrug or extremely drug resistant. Pathogens causing infections associated with invasive medical devices are biofilm producers and hence their treatment becomes difficult due to a structurally stable matrix which prevents antibiotics from penetrating the biofilm and thereby showing its effects. Factors contributing to tolerance are inhibition of penetration, restricted growth and activation of biofilm genes. Combination drug therapies has also shown potential to eradicate biofilm infections. A combination of inhaled Fosfomycin/tobramycin antibiotic strategy has been effective against Gram-negative as well as Gram positive organisms. Along with antibiotics, use of natural or synthetic adjuvants shows promising effects to treat biofilm infections. Fluroquinolone activity on biofilms is disrupted by low oxygen tension in the matrix, a strategy known as hyperbaric oxygen treatment that can enhance efficacy of antibiotics if well optimized. Adjuvants such as Ethylenediaminetetraacetic acid (EDTA), Sodium Dodecyl Sulphate (SDS) and chlorhexidine act by killing non-growing microbial cells aggregated on the inner layer of the biofilm. This review aims to list down current combination therapies used against Gram-negative and Gram-positive biofilm forming pathogens and brief about comparison of combination drugs and their efficacies.

摘要

抗生素耐药性是由抗生素过度使用、缺乏意识、生物膜形成等因素引起的全球性威胁。世界卫生组织发布了一份全球优先病原体清单,其中包括 12 种细菌,分为表达关键、高和中等耐药性的 3 类。已知几种革兰氏阴性菌和革兰氏阳性菌会引起多种感染,并已成为多药或极度耐药菌。引起与侵入性医疗设备相关感染的病原体是生物膜生产者,因此由于结构稳定的基质,它们的治疗变得困难,抗生素无法穿透生物膜并发挥作用。导致耐药性的因素包括抑制穿透、限制生长和激活生物膜基因。联合药物治疗也显示出根除生物膜感染的潜力。吸入磷霉素/妥布霉素抗生素联合治疗策略已被证明对革兰氏阴性菌和革兰氏阳性菌有效。除了抗生素外,天然或合成佐剂的使用也显示出治疗生物膜感染的有前景的效果。氟喹诺酮类药物在生物膜上的活性受到基质中低氧张力的抑制,这种策略被称为高压氧治疗,如果优化得当,可以增强抗生素的疗效。佐剂如乙二胺四乙酸(EDTA)、十二烷基硫酸钠(SDS)和洗必泰通过杀死聚集在生物膜内层的非生长微生物细胞来发挥作用。本综述旨在列出目前用于对抗革兰氏阴性菌和革兰氏阳性菌生物膜形成病原体的联合治疗方法,并简要介绍联合药物及其疗效的比较。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8614/10149696/682a4b5244fb/fcimb-13-1155699-g001.jpg

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