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Sub-nanometer Resolution Imaging with Amplitude-modulation Atomic Force Microscopy in Liquid
Published on: December 20, 2016
Are the soft, liquid-like structures detected around bacteria by ambient dynamic atomic force microscopy capsules?
A Méndez-Vilas1, L Labajos-Broncano, J Perera-Núñez
1Department of Applied Physics, University of Extremadura, Avda. Elvas s/n, 06071 Badajoz, Spain. amvilas@formatex.org
Applied and Environmental Microbiology
|March 15, 2011
Summary
Atomic force microscopy (AFM) imaging of bacterial capsules is challenging. This study reveals that liquid-like substances observed around bacteria are not capsules but are formed by buffer deliquescence, refuting their biological origin.
Area of Science:
- Microbiology
- Biophysics
- Surface Science
Background:
- Bacterial capsules are crucial virulence factors, but their imaging is difficult.
- Atomic force microscopy (AFM) has been proposed for imaging delicate bacterial capsules.
- Previous studies suggested AFM could detect liquid-like substances as bacterial capsules.
Purpose of the Study:
- To investigate the capacity of AFM for imaging bacterial capsules.
- To explore the nature of the liquid-like substances observed around staphylococcal strains using AFM.
- To determine the origin and mechanism of formation of these observed structures.
Main Methods:
- Utilized atomic force microscopy (AFM) to image three staphylococcal strains.
- Employed phosphate buffer and water as suspending liquids.
- Conducted extensive imaging and chemical analysis, including experiments with nonliving particles.
Main Results:
- AFM visualized liquid-like substances around staphylococcal strains, similar to previously reported bacterial capsules.
- Chemical analysis and experiments with nonliving particles indicated the suspending liquid (buffer) is central to substance formation.
- The phenomenon was reproduced with nonliving particles, refuting a biological origin.
Conclusions:
- The observed liquid-like structures are not bacterial capsules but result from the deliquescence of buffer components (e.g., K(2)HPO(4), CaCl(2), HEPES).
- This deliquescence mechanism explains the similarity of results across different bacterial strains and suspending liquids.
- The biological/biomedical implications of these ultrasmall liquid amounts wrapping microorganisms warrant further discussion.
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