Facility for Anti-Infective Drug Development and Innovation, Monash Institute of Pharmaceutical Sciences, Monash University, Parkville, Victoria 3052, Australia.
Antimicrob Agents Chemother. 2009 Dec;53(12):4979-86. doi: 10.1128/AAC.00497-09. Epub 2009 Sep 28.
The prevalence of infections caused by multidrug-resistant gram-negative Acinetobacter baumannii strains and the lack of novel antibiotics under development are posing a global dilemma, forcing a resurgence of the last-line antibiotic colistin. Our aim was to use atomic force microscopy (AFM) to investigate the morphology and topography of paired colistin-susceptible and -resistant cells from colistin-heteroresistant A. baumannii strains as a function of bacterial growth phase and colistin exposure. An optimal AFM bacterial sample preparation protocol was established and applied to examine three paired strains. Images revealed rod-shaped colistin-susceptible cells (1.65 +/- 0.27 microm by 0.98 +/- 0.07 microm) at mid-logarithmic phase, in contrast to spherical colistin-resistant cells (1.03 +/- 0.09 microm); the latter were also more diverse in appearance and exhibited a rougher surface topography (7.05 +/- 1.3 nm versus 11.4 +/- 2.5 nm for susceptible versus resistant, respectively). Cellular elongation up to approximately 18 microm at stationary phase was more commonly observed in susceptible strains, although these "worm-like" cells were also observed occasionally in the resistant population. The effects of colistin exposure on the cell surface of colistin-susceptible and -resistant cells were found to be similar; topographical changes were minor in response to 0.5 microg/ml colistin; however, at 4 microg/ml colistin, a significant degree of surface disruption was detected. At 32 microg/ml colistin, cellular clumping and surface smoothening were evident. Our study has demonstrated for the first time substantial morphological and topographical differences between colistin-susceptible and -resistant cells from heteroresistant A. baumannii strains. These results contribute to an understanding of colistin action and resistance in regard to this problematic pathogen.
耐多药革兰氏阴性鲍曼不动杆菌菌株感染的流行以及缺乏新的开发中的抗生素,这给全球带来了困境,迫使最后一线抗生素粘菌素重新使用。我们的目的是使用原子力显微镜(AFM)研究耐多药鲍曼不动杆菌菌株中粘菌素敏感和耐药细胞的形态和形貌,作为细菌生长阶段和粘菌素暴露的函数。建立了最佳的 AFM 细菌样品制备方案,并应用于检查三对菌株。图像显示对数中期的粘菌素敏感细胞(1.65 +/- 0.27 微米×0.98 +/- 0.07 微米)呈杆状,而粘菌素耐药细胞呈球形(1.03 +/- 0.09 微米);后者在外观上也更加多样化,表面形貌更粗糙(敏感株为 7.05 +/- 1.3nm,耐药株为 11.4 +/- 2.5nm)。在静止期,敏感株中更常见的是细胞伸长至约 18 微米,尽管耐药株中偶尔也观察到这些“虫样”细胞。粘菌素暴露对粘菌素敏感和耐药细胞表面的影响被发现相似;对 0.5μg/ml 粘菌素的反应,形貌变化较小;然而,在 4μg/ml 粘菌素时,检测到明显的表面破坏。在 32μg/ml 粘菌素时,细胞聚集和表面光滑化明显。我们的研究首次证明了耐多药鲍曼不动杆菌菌株中粘菌素敏感和耐药细胞之间存在显著的形态和形貌差异。这些结果有助于了解粘菌素在这种有问题的病原体中的作用和耐药性。