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β-内酰胺类抗生素对在恒化器中培养的缓慢生长细菌的杀菌活性评估。

Evaluation of the bactericidal activity of beta-lactam antibiotics on slowly growing bacteria cultured in the chemostat.

作者信息

Cozens R M, Tuomanen E, Tosch W, Zak O, Suter J, Tomasz A

出版信息

Antimicrob Agents Chemother. 1986 May;29(5):797-802. doi: 10.1128/AAC.29.5.797.

Abstract

The bactericidal activity of 23 beta-lactam antibiotics was compared in slowly growing bacteria cultured in a chemostat. In an attempt to mimic possible in vivo conditions, slowly growing cultures were produced by limitation of iron, glucose, phosphate, or magnesium. Only select antibiotics remained effectively bactericidal against slowly growing cells. For these compounds, the rate of antibiotic-induced loss of viability was a constant when killing was expressed per generation (in contrast to absolute time) in that slowly growing bacteria were killed proportionately more slowly. Individual antibiotics differed greatly, however, in their specific bactericidal activities against slowly growing cells, i.e., in the absolute degree of killing elicited during exposure of the bacteria to MIC equivalents of the drugs. Specific bactericidal activities varied not only with drug structure but also with the bacterial strains and, to a lesser extent, with the nature of the growth-limiting nutrient. In slowly growing cultures exposure to the low drug concentrations studied here (near MIC) caused killing without detectable lysis. Antibiotics with high specific bactericidal activities were capable of rapidly killing cultures of slowly growing pathogens despite extremely long generation times approaching those reported for in vivo growth rates.

摘要

在恒化器中培养的缓慢生长细菌中,比较了23种β-内酰胺抗生素的杀菌活性。为了模拟可能的体内条件,通过限制铁、葡萄糖、磷酸盐或镁来产生缓慢生长的培养物。只有特定的抗生素对缓慢生长的细胞仍保持有效的杀菌作用。对于这些化合物,当按每代(与绝对时间相反)表示杀菌时,抗生素诱导的活力丧失率是恒定的,因为缓慢生长的细菌被杀灭的速度相对较慢。然而,个别抗生素对缓慢生长细胞的特定杀菌活性差异很大,即在细菌暴露于药物的MIC等效浓度期间所引发的绝对杀菌程度。特定杀菌活性不仅随药物结构变化,还随细菌菌株变化,并且在较小程度上随生长限制营养素的性质变化。在缓慢生长的培养物中,暴露于此处研究的低药物浓度(接近MIC)会导致杀菌而无明显裂解。具有高特定杀菌活性的抗生素能够迅速杀死缓慢生长病原体的培养物,尽管其代时极长,接近体内生长速率的报道值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d916/284156/016eb535ae80/aac00379-0080-a.jpg

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