Hanafi Aimi, Lee Woon Ching, Loke Mun Fai, Teh Xinsheng, Shaari Ain, Dinarvand Mojdeh, Lehours Philippe, Mégraud Francis, Leow Alex Hwong Ruey, Vadivelu Jamuna, Goh Khean Lee
Department of Medical Microbiology, Faculty of Medicine, University of Malaya Kuala Lumpur, Malaysia.
Department of Medical Microbiology, Faculty of Medicine, University of MalayaKuala Lumpur, Malaysia; Department of Microbiology and Immunology, Yong Loo Lin School of Medicine, National University of SingaporeSingapore, Singapore.
Front Microbiol. 2016 Dec 15;7:2015. doi: 10.3389/fmicb.2016.02015. eCollection 2016.
Antibiotic resistance in bacteria incurs fitness cost, but compensatory mechanisms may ameliorate the cost and sustain the resistance even under antibiotics-free conditions. The aim of this study was to determine compensatory mechanisms of antibiotic resistance in . Five strains of levofloxacin-sensitive were induced to develop resistance. In addition, four pairs of metronidazole-sensitive and -resistant strains were isolated from patients carrying dual populations that consist of both sensitive and resistant phenotypes. Growth rate, virulence and biofilm-forming ability of the sensitive and resistant strains were compared to determine effects of compensatory response. Proteome profiles of paired sensitive and resistant strains were analyzed by liquid chromatography/mass spectrophotometry (LC/MS). Although there were no significant differences in growth rate between sensitive and resistant pairs, bacterial virulence (in terms of abilities to induce apoptosis and form biofilm) differs from pair to pair. These findings demonstrate the complex and strain-specific phenotypic changes in compensation for antibiotics resistance. Compensation for induced levofloxacin resistance involving mutations of and was functionally random. Furthermore, higher protein translation and non-functional protein degradation capabilities in naturally-occuring dual population metronidazole sensitive-resistant strains may be a possible alternative mechanism underlying resistance to metronidazole without mutations in and . This may explain the lack of mutations in target genes in ~10% of metronidazole resistant strains.
细菌中的抗生素耐药性会带来适应性代价,但补偿机制可能会减轻这种代价,甚至在无抗生素条件下维持耐药性。本研究的目的是确定[具体细菌名称]中抗生素耐药性的补偿机制。诱导五株左氧氟沙星敏感的[具体细菌名称]产生耐药性。此外,从携带由敏感和耐药表型组成的双重[具体细菌名称]群体的患者中分离出四对甲硝唑敏感和耐药的[具体细菌名称]菌株。比较敏感和耐药菌株的生长速率、毒力和生物膜形成能力,以确定补偿反应的影响。通过液相色谱/质谱联用(LC/MS)分析配对的敏感和耐药菌株的蛋白质组图谱。虽然敏感和耐药配对之间的生长速率没有显著差异,但细菌毒力(就诱导凋亡和形成生物膜的能力而言)因配对而异。这些发现证明了补偿抗生素耐药性的复杂且菌株特异性的表型变化。补偿诱导的左氧氟沙星耐药性涉及[具体基因名称1]和[具体基因名称2]的突变,其功能是随机的。此外,天然存在的双重群体甲硝唑敏感 - 耐药菌株中较高的蛋白质翻译和非功能性蛋白质降解能力可能是在[具体基因名称1]和[具体基因名称2]无突变情况下对甲硝唑耐药的一种可能替代机制。这可能解释了约10%的甲硝唑耐药菌株中靶基因缺乏突变的现象。