双组分调控系统(phoPQ和pmrAB)在铜绿假单胞菌多粘菌素B敏感性中的差异作用

Daniel Owusu-Anim, Dong H Kwon
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引用次数: 26

摘要

多粘菌素通常被认为是治疗耐多药铜绿假单胞菌的最后手段,但多粘菌素耐药性已越来越多地报道在世界各地的临床分离株。铜绿假单胞菌的多粘菌素耐药性已知与PhoQ或PmrB的改变有关。本研究构建了携带PhoQ和PmrB单失活和/或双失活氨基酸置换的铜绿假单胞菌突变株,以进一步了解PhoQ和PmrB在多粘菌素敏感性中的作用。多粘菌素B耐药是由PhoQ的失活和/或氨基酸取代引起的,但仅由PmrB的氨基酸取代引起。PhoQ和PmrB的改变比PhoQ或PmrB的单独改变导致更高水平的多粘菌素B抗性。这些结果被时间杀死实验证实,表明铜绿假单胞菌的高水平多粘菌素耐药性是由PhoQ和PmrB的改变引起的。
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Differential Role of Two-Component Regulatory Systems (phoPQ and pmrAB) in Polymyxin B Susceptibility of Pseudomonas aeruginosa.

Polymyxins are often considered as a last resort to treat multidrug resistant P. aeruginosa but polymyxin resistance has been increasingly reported worldwide in clinical isolates. Polymyxin resistance in P. aeruginosa is known to be associated with alterations in either PhoQ or PmrB. In this study, mutant strains of P. aeruginosa carrying amino acid substitution, a single and/or dual inactivation of PhoQ and PmrB were constructed to further understand the roles of PhoQ and PmrB in polymyxin susceptibility. Polymyxin B resistance was caused by both inactivation and/or amino acid substitutions in PhoQ but by only amino acid substitutions of PmrB. Alterations of both PhoQ and PmrB resulted in higher levels of polymyxin B resistance than alteration of either PhoQ or PmrB alone. These results were confirmed by time-killing assays suggesting that high-level polymyxin resistance in P. aeruginosa is caused by alterations of both PhoQ and PmrB.

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