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耐多粘菌素铜绿假单胞菌的外膜蛋白:镁缺乏的影响

Outer membrane proteins of polymyxin resistant Pseudomonas aeruginosa: effect of magnesium depletion.

作者信息

Shand G H, Anwar H, Brown M R

机构信息

Department of Clinical Microbiology, Rigshospitalet, Copenhagen, Denmark.

出版信息

J Antimicrob Chemother. 1988 Dec;22(6):811-21. doi: 10.1093/jac/22.6.811.

Abstract

Pseudomonas aeruginosa strain PA01, which is normally sensitive to 10 units/ml of polymyxin, was adapted in eight successive steps to be resistant to polymyxin at 6000 units/ml. The polymyxin-resistant variant was very sensitive to all other antibiotics with which it was challenged, including hydrophobic antibiotics such as erythromycin. This increased sensitivity implies that the acquired polymyxin resistance had disrupted the permeability barrier of the outer membrane. Changes in the outer membrane protein profile of PA01 were studied at each adaption step using sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE). At the third step (resistant to 80 units/ml) protein H1 was absent. At succeeding steps up to 6000 units/ml of polymyxin, protein H1 was still absent and the levels of OM proteins D, E, F (major porin) and G were all considerably reduced compared with the wild type. Overproduction of protein H1 by wild type P. aeruginosa under conditions of magnesium depletion has been proposed as a mechanism to explain polymyxin resistance. However, protein H1 remained absent from the outer membrane of the polymyxin-resistant variants even under magnesium depletion. Furthermore, protein H1 could not be induced by magnesium depletion when the resistant variant was repeatedly grown in concentrations of polymyxin as low as 10 units/ml yet, at this low concentration, the variant retained its resistance to 6000 units/ml. These observations make it unlikely that induction of protein H1 alone is a mechanism of polymyxin resistance in P. aeruginosa.

摘要

铜绿假单胞菌PA01菌株通常对10单位/毫升的多粘菌素敏感,经过连续八步适应性培养后,对6000单位/毫升的多粘菌素产生了抗性。该多粘菌素抗性变体对所有其他测试的抗生素都非常敏感,包括疏水性抗生素如红霉素。这种增加的敏感性表明获得性多粘菌素抗性破坏了外膜的通透性屏障。在每个适应性步骤中,使用十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)研究了PA01外膜蛋白谱的变化。在第三步(对80单位/毫升有抗性)时,蛋白H1缺失。在后续步骤直至对6000单位/毫升多粘菌素有抗性时,蛋白H1仍然缺失,与野生型相比,外膜蛋白D、E、F(主要孔蛋白)和G的水平均显著降低。有人提出,在镁缺乏条件下,野生型铜绿假单胞菌中蛋白H1的过量产生是解释多粘菌素抗性的一种机制。然而,即使在镁缺乏的情况下,多粘菌素抗性变体的外膜中仍不存在蛋白H1。此外,当抗性变体在低至10单位/毫升的多粘菌素浓度下反复培养时,即使在这种低浓度下,该变体仍保持对6000单位/毫升的抗性,此时蛋白H1也不能被镁缺乏诱导产生。这些观察结果表明,仅蛋白H1的诱导不太可能是铜绿假单胞菌中多粘菌素抗性的机制。

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