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Review
. 2016 Nov 5;371(1707):20150499.
doi: 10.1098/rstb.2015.0499.

Shedding light on biology of bacterial cells

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Review

Shedding light on biology of bacterial cells

Johannes P Schneider et al. Philos Trans R Soc Lond B Biol Sci. .

Abstract

To understand basic principles of living organisms one has to know many different properties of all cellular components, their mutual interactions but also their amounts and spatial organization. Live-cell imaging is one possible approach to obtain such data. To get multiple snapshots of a cellular process, the imaging approach has to be gentle enough to not disrupt basic functions of the cell but also have high temporal and spatial resolution to detect and describe the changes. Light microscopy has become a method of choice and since its early development over 300 years ago revolutionized our understanding of living organisms. As most cellular components are indistinguishable from the rest of the cellular contents, the second revolution came from a discovery of specific labelling techniques, such as fusions to fluorescent proteins that allowed specific tracking of a component of interest. Currently, several different tags can be tracked independently and this allows us to simultaneously monitor the dynamics of several cellular components and from the correlation of their dynamics to infer their respective functions. It is, therefore, not surprising that live-cell fluorescence microscopy significantly advanced our understanding of basic cellular processes. Current cameras are fast enough to detect changes with millisecond time resolution and are sensitive enough to detect even a few photons per pixel. Together with constant improvement of properties of fluorescent tags, it is now possible to track single molecules in living cells over an extended period of time with a great temporal resolution. The parallel development of new illumination and detection techniques allowed breaking the diffraction barrier and thus further pushed the resolution limit of light microscopy. In this review, we would like to cover recent advances in live-cell imaging technology relevant to bacterial cells and provide a few examples of research that has been possible due to imaging.This article is part of the themed issue 'The new bacteriology'.

Keywords: bacteria; imaging; live cells.

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References

    1. Hardham AR. 2012. Confocal microscopy in plant-pathogen interactions. Methods Mol. Biol. 835, 295–309. (10.1007/978-1-61779-501-5_18) - DOI - PubMed
    1. Bain J, Gow NA, Erwig LP. 2015. Novel insights into host-fungal pathogen interactions derived from live-cell imaging. Semin. Immunopathol. 37, 131–139. (10.1007/s00281-014-0463-3) - DOI - PMC - PubMed
    1. Lepanto P, Lecumberry F, Rossello J, Kierbel A. 2014. A confocal microscopy image analysis method to measure adhesion and internalization of Pseudomonas aeruginosa multicellular structures into epithelial cells. Mol. Cell. Probes 28, 1–5. (10.1016/j.mcp.2013.10.001) - DOI - PubMed
    1. Bjarnsholt T, Ciofu O, Molin S, Givskov M, Hoiby N. 2013. Applying insights from biofilm biology to drug development: can a new approach be developed? Nat. Rev. Drug Discov. 12, 791–808. (10.1038/nrd4000) - DOI - PubMed
    1. Kirker KR, Fisher ST, James GA. 2015. Potency and penetration of telavancin in staphylococcal biofilms. Int. J. Antimicrob. Agents 46, 451–455. (10.1016/j.ijantimicag.2015.05.022) - DOI - PubMed

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