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Pan-transcriptomic analysis identified common differentially expressed genes of Acinetobacter baumannii in response to polymyxin treatments

机译:Pan-transcriptomic分析识别常见的不动杆菌的差异表达基因baumannii多粘菌素治疗的反应

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Multidrug-resistant Acinetobacter baumannii is a top-priority Gram-negative pathogen and polymyxins are a last-line therapeutic option. Previous systems pharmacological studies examining polymyxin killing and resistance usually focused on individual strains, and the derived knowledge could be limited by strain-specific genomic context. In this study, we examined the gene expression of five A. baumannii strains (34654, 1207552, 1428368, 1457504 and ATCC 19606) to determine the common differentially expressed genes in response to polymyxin treatments. A pan-genome containing 6061 genes was identified for 89 A. baumannii genomes from RefSeq database which included the five strains examined in this study; 2822 of the 6061 genes constituted the core genome. After 2 mg L~(-1) or 0.75 × MIC polymyxin treatments for 15 min, 41 genes were commonly up-regulated, including those involved in membrane biogenesis and homeostasis, lipoprotein and phospholipid trafficking, efflux pump and poly-N-acetylglucosamine biosynthesis; six genes were commonly down-regulated, three of which were related to fatty acid biosynthesis. Additionally, comparison of the gene expression at 15 and 60 min in ATCC 19606 revealed that polymyxin treatment resulted in a rapid change in amino acid metabolism at 15 min and perturbations on envelope biogenesis at both time points. This is the first pan- transcriptomic study for polymyxin-treated A. baumannii and our results identified that the remodelled outer membrane, up-regulated efflux pumps and down-regulated fatty acid biosynthesis might be essential for early responses to polymyxins in A. baumannii. Our findings provide important mechanistic insights into bacterial responses to polymyxin killing and may facilitate the optimisation of polymyxin therapy against this problematic ‘superbug’.
机译:鲍曼不动杆菌是一种耐多药最优先的革兰氏阴性病菌,多粘菌素是最后防线的治疗选择。以前的系统药理研究检查多粘菌素杀戮和阻力通常集中在个人压力,派生的知识可能是有限的毒株特异性基因背景。我们检查了5个的基因表达。baumannii菌株(34654,1207552,1428368,1457504和写明ATCC 19606)确定常见差异表达基因在回应多粘菌素治疗。6061个基因被确定为89 a . baumannii其中包括从RefSeq基因组数据库在这项研究中五株检查;6061个基因构成的核心基因组。mg L ~(1)或0.75×麦克风多粘菌素治疗普遍上调基因15分钟,41岁,包括那些参与膜生物起源和体内平衡,脂蛋白和磷脂走私、射流泵和poly-N-acetylglucosamine生物合成;常见的衰减,三是吗脂肪酸生物合成有关。比较基因表达的15 - 60写明ATCC 19606分钟在显示多粘菌素治疗导致氨基酸快速变化酸代谢在15分钟和扰动在这两个时间点信封生源论。第一个锅——转录组研究polymyxin-treated a baumannii和我们的结果确定改建外膜,向上调节射流泵和衰减脂肪酸生物合成可能是必不可少的答:baumannii早期对多粘菌素的反应。我们的研究结果提供了重要的机械洞察细菌对多粘菌素的反应杀戮和可能促进优化多粘菌素治疗对这个问题‘superbug’。

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