Diniz Claudio Galuppo, Farias Luiz M, Carvalho Maria Auxiliadora R, Rocha Edson R, Smith C Jeffrey
Department of Microbiology and Immunology, The Brody School of Medicine, East Carolina University, Greenville, NC, USA.
J Antimicrob Chemother. 2004 Jul;54(1):100-8. doi: 10.1093/jac/dkh256. Epub 2004 May 18.
The current work focused on molecular changes in a spontaneous Bacteroides fragilismutant selected by low concentrations of metronidazole as an adaptive response to the drug.
A metronidazole-resistant strain derived from B. fragilis ATCC 25285 was selected by passage in the presence of drug using 0-4 mg/L gradient plates. Using a combination of proteomics for identification of differentially expressed proteins by two-dimensional electrophoresis and selected mutational analyses by single cross-over insertion and an allelic exchange, we have identified genes involved in the adaptive response to metronidazole.
There are significant changes in the protein profiles of resistant strains. These changes appeared to affect a wide range of metabolic proteins including lactate dehydrogenase (up-regulated) and flavodoxin (down-regulated), which may be involved in electron transfer reactions. Also, the enzymic activity of the pyruvate-ferredoxin oxidoreductase (PorA) complex was impaired. Mutant strains lacking the genes for flavodoxin and PorA were less susceptible to metronidazole than the sensitive parent, and a double flavodoxin/PorA mutant had even less susceptibility but none of the mutants were as resistant as the spontaneous metronidazole-resistant strain.
Overall, the data indicated that there were global changes in the regulation of the physiology of the metronidazole-resistant strain. In addition, flavodoxin was identified as an important contributor to metronidazole sensitivity in B. fragilis.
当前研究聚焦于脆弱拟杆菌自发突变体的分子变化,该突变体是通过低浓度甲硝唑筛选出来的,作为对药物的适应性反应。
从脆弱拟杆菌ATCC 25285衍生出的耐甲硝唑菌株,是通过在含0 - 4 mg/L梯度平板的药物存在下传代筛选得到的。我们结合蛋白质组学通过二维电泳鉴定差异表达蛋白,以及通过单交换插入和等位基因交换进行选定的突变分析,来确定参与对甲硝唑适应性反应的基因。
耐药菌株的蛋白质谱有显著变化。这些变化似乎影响了广泛的代谢蛋白,包括乳酸脱氢酶(上调)和黄素氧还蛋白(下调),它们可能参与电子传递反应。此外,丙酮酸 - 铁氧还蛋白氧化还原酶(PorA)复合物的酶活性受损。缺乏黄素氧还蛋白和PorA基因的突变菌株比敏感亲本对甲硝唑的敏感性更低,而黄素氧还蛋白/ PorA双突变体的敏感性更低,但没有一个突变体像自发耐甲硝唑菌株那样耐药。
总体而言,数据表明耐甲硝唑菌株的生理调节存在全局性变化。此外,黄素氧还蛋白被确定为脆弱拟杆菌对甲硝唑敏感性的重要贡献因素。