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The use of SWATH to analyse the dynamic changes of bacterial proteome of carbapanemase-producing Escherichia coli under antibiotic pressure

机译:利用SWATH分析在抗生素压力下产生碳巴巴胺酶的大肠杆菌细菌蛋白质组的动态变化

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摘要

Antibiotic resistance associated with the clinically significant carbapenemases KPC, NDM and OXA-48 in Enterobacteriaceae is emerging as worldwide. In Australia, IMP-producing Enterobacteriaceae are the most prevalent carbapenemase-producing Enterobacteriaceae (CPE). Genomic characteristics of such CPE are well described, but the corresponding proteome is poorly characterised. We have thus developed a method to analyse dynamic changes in the proteome of CPE under antibiotic pressure. Specifically, we have investigated the effect of meropenem at sub-lethal concentrations to develop a better understanding of how antibiotic pressure leads to resistance. Escherichia coli strains producing either NDM-, IMP- or KPC-type carbapenemases were included in this study, and their proteomes were analysed in growth conditions with or without meropenem. The most significant difference in the bacterial proteomes upon the addition of meropenem was triggered amongst NDM-producers and to a lower extent amongst KPC-producers. In particular, HU DNA-binding proteins, the GroEL/GroES chaperonin complex and GrpE proteins were overexpressed. These proteins may thus contribute to the better adaptability of NDM- and KPC-producers to meropenem. A significant meropenem-induced increase in the expression of the outer membrane protein A was only observed in IMP-producers, thus demonstrating that carbapenemase-mediated resistance relies on far more complex mechanisms than simple inactivation of the antibiotic.
机译:与肠杆菌科中具有临床意义的碳青霉烯酶KPC,NDM和OXA-48相关的抗生素耐药性正在全球范围内兴起。在澳大利亚,产生IMP的肠杆菌科是最流行的产生碳青霉烯酶的肠杆菌科(CPE)。很好地描述了这种CPE的基因组特征,但是相应的蛋白质组的表征却很差。因此,我们开发了一种分析抗生素压力下CPE蛋白质组动态变化的方法。具体来说,我们已经研究了美罗培南在亚致死浓度下的作用,以更好地了解抗生素压力如何导致耐药性。产生NDM型,IMP型或KPC型碳青霉烯酶的大肠杆菌菌株均包括在本研究中,并在有或没有美罗培南的生长条件下分析了它们的蛋白质组。在添加美罗培南后,细菌蛋白质组的最显着差异是在NDM生产者中引发的,而在KPC生产者中引发的差异则较小。特别是,HU DNA结合蛋白,GroEL / GroES伴侣蛋白复合物和GrpE蛋白被过表达。因此,这些蛋白质可能有助于NDM和KPC生产者更好地适应美罗培南。仅在IMP生产者中观察到美罗培南诱导的外膜蛋白A表达的显着增加,因此表明碳青霉烯酶介导的抗药性比简单的灭活抗生素依赖的机理要复杂得多。

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