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Microfluidic Cultivation and Laser Tweezers Raman Spectroscopy of E. coli under Antibiotic Stress

Z. Pilát, S. Bernatová, J. Ježek, J. Kirchhoff, A. Tannert, U. Neugebauer, O. Samek, P. Zemánek,

. 2018 ; 18 (5) : . [pub] 20180518

Language English Country Switzerland

Document type Journal Article

Analyzing the cells in various body fluids can greatly deepen the understanding of the mechanisms governing the cellular physiology. Due to the variability of physiological and metabolic states, it is important to be able to perform such studies on individual cells. Therefore, we developed an optofluidic system in which we precisely manipulated and monitored individual cells of Escherichia coli. We tested optical micromanipulation in a microfluidic chamber chip by transferring individual bacteria into the chambers. We then subjected the cells in the chambers to antibiotic cefotaxime and we observed the changes by using time-lapse microscopy. Separately, we used laser tweezers Raman spectroscopy (LTRS) in a different micro-chamber chip to manipulate and analyze individual cefotaxime-treated E. coli cells. Additionally, we performed conventional Raman micro-spectroscopic measurements of E. coli cells in a micro-chamber. We found observable changes in the cellular morphology (cell elongation) and in Raman spectra, which were consistent with other recently published observations. The principal component analysis (PCA) of Raman data distinguished between the cefotaxime treated cells and control. We tested the capabilities of the optofluidic system and found it to be a reliable and versatile solution for this class of microbiological experiments.

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$a Pilát, Zdeněk $u Institute of Scientific Instruments (ISI), Czech Academy of Sciences, v.v.i., Kralovopolska 147, 612 64 Brno, Czech Republic. pilat@isibrno.cz.
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$a Analyzing the cells in various body fluids can greatly deepen the understanding of the mechanisms governing the cellular physiology. Due to the variability of physiological and metabolic states, it is important to be able to perform such studies on individual cells. Therefore, we developed an optofluidic system in which we precisely manipulated and monitored individual cells of Escherichia coli. We tested optical micromanipulation in a microfluidic chamber chip by transferring individual bacteria into the chambers. We then subjected the cells in the chambers to antibiotic cefotaxime and we observed the changes by using time-lapse microscopy. Separately, we used laser tweezers Raman spectroscopy (LTRS) in a different micro-chamber chip to manipulate and analyze individual cefotaxime-treated E. coli cells. Additionally, we performed conventional Raman micro-spectroscopic measurements of E. coli cells in a micro-chamber. We found observable changes in the cellular morphology (cell elongation) and in Raman spectra, which were consistent with other recently published observations. The principal component analysis (PCA) of Raman data distinguished between the cefotaxime treated cells and control. We tested the capabilities of the optofluidic system and found it to be a reliable and versatile solution for this class of microbiological experiments.
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$a Bernatová, Silvie $u Institute of Scientific Instruments (ISI), Czech Academy of Sciences, v.v.i., Kralovopolska 147, 612 64 Brno, Czech Republic. berns@isibrno.cz.
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$a Ježek, Jan $u Institute of Scientific Instruments (ISI), Czech Academy of Sciences, v.v.i., Kralovopolska 147, 612 64 Brno, Czech Republic. jezek@isibrno.cz.
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$a Kirchhoff, Johanna $u Center for Sepsis Control and Care (CSCC), Jena University Hospital, Am Klinikum 1, D-07747 Jena, Germany. Johanna.Kirchhoff@med.uni-jena.de. Institute of Physical Chemistry, Friedrich Schiller University Jena, Helmholtzweg 4, D-07743 Jena, Germany. Johanna.Kirchhoff@med.uni-jena.de. Leibniz Institute of Photonic Technology (Leibniz IPHT), Albert-Einstein-Str. 9, D-07745 Jena, Germany. Johanna.Kirchhoff@med.uni-jena.de.
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$a Tannert, Astrid $u Center for Sepsis Control and Care (CSCC), Jena University Hospital, Am Klinikum 1, D-07747 Jena, Germany. Astrid.Tannert@med.uni-jena.de. Leibniz Institute of Photonic Technology (Leibniz IPHT), Albert-Einstein-Str. 9, D-07745 Jena, Germany. Astrid.Tannert@med.uni-jena.de.
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$a Neugebauer, Ute $u Center for Sepsis Control and Care (CSCC), Jena University Hospital, Am Klinikum 1, D-07747 Jena, Germany. ute.neugebauer@med.uni-jena.de. Institute of Physical Chemistry, Friedrich Schiller University Jena, Helmholtzweg 4, D-07743 Jena, Germany. ute.neugebauer@med.uni-jena.de. Leibniz Institute of Photonic Technology (Leibniz IPHT), Albert-Einstein-Str. 9, D-07745 Jena, Germany. ute.neugebauer@med.uni-jena.de.
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$a Samek, Ota $u Institute of Scientific Instruments (ISI), Czech Academy of Sciences, v.v.i., Kralovopolska 147, 612 64 Brno, Czech Republic. osamek@isibrno.cz.
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$a Zemánek, Pavel $u Institute of Scientific Instruments (ISI), Czech Academy of Sciences, v.v.i., Kralovopolska 147, 612 64 Brno, Czech Republic. pavlik@isibrno.cz.
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