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抗生素磷霉素通过模拟中间代谢产物磷酸烯醇丙酮酸和 3-磷酸甘油醛的作用来影响转录组。

The Antibiotic Fosfomycin Mimics the Effects of the Intermediate Metabolites Phosphoenolpyruvate and Glyceraldehyde-3-Phosphate on the Transcriptome.

机构信息

Centro Nacional de Biotecnología, CSIC, Darwin 3, 28049 Madrid, Spain.

Programa de Doctorado en Biociencias Moleculares, Universidad Autónoma de Madrid, 28049 Madrid, Spain.

出版信息

Int J Mol Sci. 2021 Dec 23;23(1):159. doi: 10.3390/ijms23010159.

Abstract

is an opportunistic pathogen with an environmental origin, which presents a characteristically low susceptibility to antibiotics and is capable of acquiring increased levels of resistance to antimicrobials. Among these, fosfomycin resistance seems particularly intriguing; resistance to this antibiotic is generally due to the activity of fosfomycin-inactivating enzymes, or to defects in the expression or the activity of fosfomycin transporters. In contrast, we previously described that the cause of fosfomycin resistance in was the inactivation of enzymes belonging to its central carbon metabolism. To go one step further, here we studied the effects of fosfomycin on the transcriptome of compared to those of phosphoenolpyruvate-its structural homolog-and glyceraldehyde-3-phosphate-an intermediate metabolite of the mutated route in fosfomycin-resistant mutants. Our results show that transcriptomic changes present a large degree of overlap, including the activation of the cell-wall-stress stimulon. These results indicate that fosfomycin activity and resistance are interlinked with bacterial metabolism. Furthermore, we found that the studied compounds inhibit the expression of the efflux pump, which confers intrinsic resistance to aminoglycosides. This is the first description of efflux pump inhibitors that can be used as antibiotic adjuvants to counteract antibiotic resistance in .

摘要

是一种具有环境起源的机会性病原体,其对抗生素的敏感性通常较低,并且能够获得对抗微生物药物的更高水平的耐药性。在这些耐药性中,磷霉素耐药性似乎特别有趣;这种抗生素的耐药性通常是由于磷霉素失活酶的活性,或磷霉素转运蛋白的表达或活性缺陷所致。相比之下,我们之前描述了 中磷霉素耐药性的原因是其中心碳代谢酶的失活。更进一步,在这里我们研究了磷霉素对 转录组的影响,与磷酸烯醇丙酮酸(其结构类似物)和甘油醛-3-磷酸(磷霉素耐药突变体中突变途径的中间代谢物)相比。我们的结果表明,转录组变化具有很大的重叠性,包括细胞壁应激刺激物的激活。这些结果表明,磷霉素的活性和耐药性与细菌代谢密切相关。此外,我们发现研究化合物抑制了 外排泵的表达,这赋予了对氨基糖苷类药物的固有耐药性。这是首次描述可作为抗生素佐剂用于对抗 的抗生素耐药性的外排泵抑制剂。

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