SEM Analysis of Surface Impact on Biofilm Antibiotic Treatment.
Luciana Calheiros GomesFilipe José MergulhãoPublished in: Scanning (2017)
The aim of this work was to use scanning electron microscopy (SEM) to investigate the effect of ampicillin treatment on Escherichia coli biofilms formed on two surface materials with different properties, silicone (SIL) and glass (GLA). Epifluorescence microscopy (EM) was initially used to assess biofilm formation and killing efficiency on both surfaces. This technique showed that higher bacterial colonization was obtained in the hydrophobic SIL than in the hydrophilic GLA. It has also shown that higher biofilm inactivation was attained for GLA after the antibiotic treatment (7-log reduction versus 1-log reduction for SIL). Due to its high resolution and magnification, SEM enabled a more detailed analysis of the antibiotic effect on biofilm cells, complementing the killing efficiency information obtained by EM. SEM micrographs revealed that ampicillin-treated cells have an elongated form when compared to untreated cells. Additionally, it has shown that different materials induced different levels of elongation on cells exposed to antibiotic. Biofilms formed on GLA showed a 37% higher elongation than those formed on SIL. Importantly, cell elongation was related to viability since ampicillin had a higher bactericidal effect on GLA-formed biofilms. These findings raise the possibility of using SEM for understanding the efficacy of antimicrobial treatments by observation of biofilm morphology.
Keyphrases
- biofilm formation
- candida albicans
- staphylococcus aureus
- induced apoptosis
- pseudomonas aeruginosa
- escherichia coli
- high resolution
- cell cycle arrest
- endoplasmic reticulum stress
- electron microscopy
- stem cells
- signaling pathway
- healthcare
- single cell
- mass spectrometry
- optical coherence tomography
- oxidative stress
- single molecule
- high throughput
- bone marrow
- mesenchymal stem cells
- high glucose
- pi k akt
- smoking cessation
- newly diagnosed
- replacement therapy
- multidrug resistant