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A manganese photosensitive tricarbonyl molecule Mn(CO)3(tpa-κ3N)Br enhances antibiotic efficacy in a multi-drug-resistant Escherichia coli

机译:锰光敏性三羰基分子Mn(CO)3(tpa-κ3N) Br增强耐多药大肠杆菌的功效

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摘要

Carbon monoxide-releasing molecules (CORMs) are a promising class of new antimicrobials, with multiple modes of action that are distinct from those of standard antibiotics. The relentless increase in antimicrobial resistance, exacerbated by a lack of new antibiotics, necessitates a better understanding of how such novel agents act and might be used synergistically with established antibiotics. This work aimed to understand the mechanism(s) underlying synergy between a manganese-based photoactivated carbon monoxide-releasing molecule (PhotoCORM), [Mn(CO)3(tpa-κ3N)]Br [tpa=tris(2-pyridylmethyl)amine], and various classes of antibiotics in their activities towards Escherichia coli EC958, a multi-drug-resistant uropathogen. The title compound acts synergistically with polymyxins [polymyxin B and colistin (polymyxin E)] by damaging the bacterial cytoplasmic membrane. [Mn(CO)3(tpa-κ3N)]Br also potentiates the action of doxycycline, resulting in reduced expression of tetA, which encodes a tetracycline efflux pump. We show that, like tetracyclines, the breakdown products of [Mn(CO)3(tpa-κ3N)]Br activation chelate iron and trigger an iron starvation response, which we propose to be a further basis for the synergies observed. Conversely, media supplemented with excess iron abrogated the inhibition of growth by doxycycline and the title compound. In conclusion, multiple factors contribute to the ability of this PhotoCORM to increase the efficacy of antibiotics in the polymyxin and tetracycline families. We propose that light-activated carbon monoxide release is not the sole basis of the antimicrobial activities of [Mn(CO)3(tpa-κ3N)]Br.
机译:一氧化碳释放分子(CORMs)是一类有前景的新型抗菌剂,具有不同于标准抗生素的多种作用方式。由于缺乏新的抗生素而加剧的抗药性的不断提高,需要更好地了解这种新型药物的作用方式,并可以与已建立的抗生素协同使用。这项工作旨在了解基于锰的光活化一氧化碳释放分子(PhotoCORM)[Mn(CO)3(tpa-κ 3 N)] Br [ tpa = tris(2-pyridylmethylmethylamine)]和各种抗生素对大肠杆菌EC958(一种具有多重耐药性的尿路致病菌)的活性。标题化合物通过破坏细菌的细胞质膜与多粘菌素[多粘菌素B和粘菌素(多粘菌素E)]协同作用。 [Mn(CO)3(tpa-κ 3 N)] Br还增强强力霉素的作用,导致tetA的表达减少,该蛋白编码四环素外排泵。我们表明,像四环素一样,[Mn(CO)3(tpa-κ 3 N)] Br活化的螯合螯合铁并触发铁饥饿反应,我们建议将其进一步观察到的协同作用的基础。相反,补充有过量铁的培养基消除了强力霉素和标题化合物对生长的抑制作用。总之,多种因素有助于该PhotoCORM增加多粘菌素和四环素家族中抗生素的功效。我们认为光活化一氧化碳的释放不是[Mn(CO)3(tpa-κ 3 N)] Br抗菌活性的唯一依据。

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