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首页> 外文期刊>Journal of applied microbiology >outer membrane protein shifts in biocide-resistant pseudomonas aeruginosa PA01
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outer membrane protein shifts in biocide-resistant pseudomonas aeruginosa PA01

机译:杀菌剂抗性铜绿假单胞菌PA01中的外膜蛋白转移

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Benzisothiazolone(BIT), N-methylisothiazolone(MIT) and 5-chloro-N-methylisothiazolone (CMIT) are highly effective biocidal agents and are used as preservatives in a variety of cosmetic preparations. The isothiazolones have proven efficacy against many fungal and bacterial species including Pseudomonas aeruginosa. However, some species are beginning to exhibit resistance towards this group of compounds after extended exposure. This experiment induced resistance in cultures of Ps. aeruginosa exposed to incrementally increasing sub-minimum inhibitory concentrations (MICs) of the isothiazolones in their pure chemical forms. The induced resistance was observed as a gradual increase in MIC with each new passage. The MICs for all three test isothiazolones and a thiol-interactive control compound (thiomersal) increased by approximately twofold during the course of the experiment. The onset of resistance was also observed by reference to the altered presence of an outer membrane protein, designated the T-OMP, in SDS-PAGe preparations. T-OMP was observed to disappear from the biocide-exposed preparations and reappear when the resistance-induced cultures were passaged in the absence of biocide. This reappearance of T-OMP was not accompanied by a complete reversal of induced resistance, but by a small decrease in MIC. The induction of resistance towards one biocide resulted in the development of cross-resistance towards other members of the group and the control, thiomersal. it has been suggested that the disappearance of T-OMp from these preparations is associated with the onset of resistance to the isothiazolones in their Kathon~TM from (CMIT and MIT).
机译:苯并异噻唑酮(BIT),N-甲基异噻唑酮(MIT)和5-氯-N-甲基异噻唑酮(CMIT)是高效的杀菌剂,并在多种化妆品制剂中用作防腐剂。异噻唑酮已被证明对包括铜绿假单胞菌在内的许多真菌和细菌种类有效。但是,某些物种在长期暴露后开始对这类化合物表现出抗药性。该实验在Ps培养物中诱导抗性。铜绿假单胞菌以纯化学形式暴露于异噻唑酮的亚最低抑制浓度(MICs)的逐渐升高。随着每一次新传代,观察到的诱导抗性是MIC逐渐增加。在实验过程中,所有三种测试异噻唑酮和硫醇相互作用的对照化合物(硫柳汞)的MIC均增加了大约两倍。通过参考SDS-PAGe制剂中外膜蛋白(称为T-OMP)的存在变化,也观察到了耐药性的发作。观察到T-OMP从暴露于杀生物剂的制剂中消失,并在不存在杀生物剂的情况下使抗性诱导的培养物传代时重新出现。 T-OMP的这种重新出现并不伴随着诱导抗性的完全逆转,而是MIC的小幅下降。对一种杀生物剂产生抗药性导致对该组其他成员和对照硫柳汞产生交叉抗药性。已经提出,这些制剂中T-OMp的消失与来自(CMIT和MIT)的Kathon TM中对异噻唑酮类的抗药性的发作有关。

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