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Identification of individual biofilm-forming bacterial cells using Raman tweezers
O. Samek, S. Bernatová, J. Ježek, M. Šiler, M. Šerý, V. Krzyžánek, K. Hrubanová, P. Zemánek, V. Holá, F. Růžička,
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
Grant support
NT13242
MZ0
CEP Register
Digital library NLK
Full text - Article
Source
NLK
PubMed Central
from 2009
Europe PubMed Central
from 2009 to 1 year ago
ROAD: Directory of Open Access Scholarly Resources
from 1998
- MeSH
- Algorithms MeSH
- Principal Component Analysis MeSH
- Bacteria metabolism MeSH
- Biofilms * MeSH
- Cell Adhesion MeSH
- Phagocytosis MeSH
- Bacterial Physiological Phenomena MeSH
- Optical Tweezers * MeSH
- Polysaccharides chemistry MeSH
- Spectrum Analysis, Raman * MeSH
- Staphylococcus epidermidis metabolism MeSH
- Hot Temperature MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
A method for in vitro identification of individual bacterial cells is presented. The method is based on a combination of optical tweezers for spatial trapping of individual bacterial cells and Raman microspectroscopy for acquisition of spectral “Raman fingerprints” obtained from the trapped cell. Here, Raman spectra were taken from the biofilm-forming cells without the influence of an extracellular matrix and were compared with biofilm-negative cells. Results of principal component analyses of Raman spectra enabled us to distinguish between the two strains of Staphylococcus epidermidis. Thus, we propose that Raman tweezers can become the technique of choice for a clearer understanding of the processes involved in bacterial biofilms which constitute a highly privileged way of life for bacteria, protected from the external environment.
References provided by Crossref.org
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- $a A method for in vitro identification of individual bacterial cells is presented. The method is based on a combination of optical tweezers for spatial trapping of individual bacterial cells and Raman microspectroscopy for acquisition of spectral “Raman fingerprints” obtained from the trapped cell. Here, Raman spectra were taken from the biofilm-forming cells without the influence of an extracellular matrix and were compared with biofilm-negative cells. Results of principal component analyses of Raman spectra enabled us to distinguish between the two strains of Staphylococcus epidermidis. Thus, we propose that Raman tweezers can become the technique of choice for a clearer understanding of the processes involved in bacterial biofilms which constitute a highly privileged way of life for bacteria, protected from the external environment.
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