The innovation of cryo-SEM freeze-fracturing methodology demonstrated on high pressure frozen biofilm. (July 2018)

• Record Type: Journal Article
• Authors: Hrubanova, Kamila; Nebesarova, Jana; Ruzicka, Filip; Krzyzanek, Vladislav
• Is Part Of: Micron. Volume 110(2018)
• Page Start: 28
• Page End: 35
• Publication Date: 2018-07
• Subjects: cryo-SEM -- High-pressure freezing (HPF) -- Freeze-fracturing -- Biofilm -- Candida -- Staphylococcus; Microscopy -- Periodicals; Electron Probe Microanalysis -- Periodicals; Microscopy -- Periodicals; Microscopie -- Périodiques; Microscopy; Periodicals; 502.82
• DOI: 10.1016/j.micron.2018.04.006
• Languages: English
• ISSNs: 0968-4328

Abstract

Highlights: New methodology for cryo-SEM investigation of samples requiring a sapphire disc as a substrate. Combination of high-pressure freezing (HPF) and perpendicular freeze-fracturing with cryo-SEM. Unusual applications of the HPF EMPACT2 for cryo-SEM imaging. A technique demonstrated on microbial biofilms significant for clinical microbiology. Abstract: In this study we present an innovative method for the preparation of fully hydrated samples of microbial biofilms of cultures Staphylococcus epidermidis, Candida parapsilosis and Candida albicans . Cryo-scanning electron microscopy (cryo-SEM) and high-pressure freezing (HPF) rank among cutting edge techniques in the electron microscopy of hydrated samples such as biofilms. However, the combination of these techniques is not always easily applicable. Therefore, we present a method of combining high-pressure freezing using EM PACT2 (Leica Microsystems), which fixes hydrated samples on small sapphire discs, with a high resolution SEM equipped with the widely used cryo-preparation system ALTO 2500 (Gatan). Using a holder developed in house, a freeze-fracturing technique was applied to image and investigate microbial cultures cultivated on the sapphire discs. In our experiments, we focused on the ultrastructure of the extracellular matrix produced during cultivation and the relationships among microbial cells in the biofilm. The main goal of our investigations was the detailed visualization of areas of the biofilm where the microbial cells adhere to the substrate/surface. We show the feasibility of this technique, which is clearly demonstrated in experiments with various freeze-etching times.