Uzoechi Samuel C, Abu-Lail Nehal I
Gene and Linda Voiland School of Chemical Engineering and Bioengineering,Washington State University,Pullman, WA 99164,USA.
Department of Biomedical Engineering,The University of Texas at San Antonio,San Antonio, TX 78249,USA.
Microsc Microanal. 2019 Feb;25(1):135-150. doi: 10.1017/S1431927618015696.
Possible multidrug-resistant (MDR) mechanisms of four resistant strains of Escherichia coli to a model β-lactam, ampicillin, were investigated using contact angle measurements of wettability, crystal violet assays of permeability, biofilm formation, fluorescence imaging, and nanoscale analyses of dimensions, adherence, and roughness. Upon exposure to ampicillin, one of the resistant strains, E. coli A5, changed its phenotype from elliptical to spherical, maintained its roughness and biofilm formation abilities, decreased its length and surface area, maintained its cell wall integrity, increased its hydrophobicity, and decreased its nanoscale adhesion to a model surface of silicon nitride. Such modifications are suggested to allow these cells to conserve energy during metabolic dormancy. In comparison, resistant strains E. coli D4, A9, and H5 elongated their cells, increased their roughness, increased their nanoscale adhesion forces, became more hydrophilic, and increased their biofilm formation upon exposure to ampicillin. These results suggest that these strains resisted ampicillin through biofilm formation that possibly introduces diffusion limitations to antibiotics. Investigations of how MDR bacterial cells modify their surfaces in response to antibiotics can guide research efforts aimed at designing more effective antibiotics and new treatment strategies for MDR bacterial infections.
利用润湿性接触角测量、通透性结晶紫测定、生物膜形成、荧光成像以及尺寸、粘附和粗糙度的纳米级分析,研究了四株大肠杆菌对模型β-内酰胺类抗生素氨苄西林的可能多重耐药(MDR)机制。在接触氨苄西林后,其中一株耐药菌株大肠杆菌A5的表型从椭圆形变为球形,保持其粗糙度和生物膜形成能力,缩短其长度和表面积,维持其细胞壁完整性,增加其疏水性,并降低其与氮化硅模型表面的纳米级粘附力。这些修饰被认为可使这些细胞在代谢休眠期间保存能量。相比之下,耐药菌株大肠杆菌D4、A9和H5在接触氨苄西林后细胞伸长,粗糙度增加,纳米级粘附力增加,变得更亲水,并增加其生物膜形成。这些结果表明,这些菌株通过生物膜形成来抵抗氨苄西林,而生物膜形成可能会给抗生素带来扩散限制。研究多重耐药细菌细胞如何响应抗生素改变其表面,可为旨在设计更有效抗生素和多重耐药细菌感染新治疗策略的研究工作提供指导。