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      A unique self-organization of bacterial sub-communities creates iridescence in Cellulophaga lytica colony biofilms

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          Abstract

          Iridescent color appearances are widespread in nature. They arise from the interaction of light with micron- and submicron-sized physical structures spatially arranged with periodic geometry and are usually associated with bright angle-dependent hues. Iridescence has been reported for many animals and marine organisms. However, iridescence has not been well studied in bacteria. Recently, we reported a brilliant “pointillistic” iridescence in colony biofilms of marine Flavobacteria that exhibit gliding motility. The mechanism of their iridescence is unknown. Here, using a multi-disciplinary approach, we show that the cause of iridescence is a unique periodicity of the cell population in the colony biofilm. Cells are arranged together to form hexagonal photonic crystals. Our model highlights a novel pattern of self-organization in a bacterial biofilm. ”Pointillistic” bacterial iridescence can be considered a new light-dependent phenomenon for the field of microbiology.

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          Most cited references36

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          Use of the Hough transformation to detect lines and curves in pictures

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            Photonic structures in biology.

            Millions of years before we began to manipulate the flow of light using synthetic structures, biological systems were using nanometre-scale architectures to produce striking optical effects. An astonishing variety of natural photonic structures exists: a species of Brittlestar uses photonic elements composed of calcite to collect light, Morpho butterflies use multiple layers of cuticle and air to produce their striking blue colour and some insects use arrays of elements, known as nipple arrays, to reduce reflectivity in their compound eyes. Natural photonic structures are providing inspiration for technological applications.
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              Growth phenotypes of Pseudomonas aeruginosa lasR mutants adapted to the airways of cystic fibrosis patients.

              The opportunistic pathogen Pseudomonas aeruginosa undergoes genetic change during chronic airway infection of cystic fibrosis (CF) patients. One common change is a mutation inactivating lasR, which encodes a transcriptional regulator that responds to a homoserine lactone signal to activate expression of acute virulence factors. Colonies of lasR mutants visibly accumulated the iridescent intercellular signal 4-hydroxy-2-heptylquinoline. Using this colony phenotype, we identified P. aeruginosa lasR mutants that emerged in the airway of a CF patient early during chronic infection, and during growth in the laboratory on a rich medium. The lasR loss-of-function mutations in these strains conferred a growth advantage with particular carbon and nitrogen sources, including amino acids, in part due to increased expression of the catabolic pathway regulator CbrB. This growth phenotype could contribute to selection of lasR mutants both on rich medium and within the CF airway, supporting a key role for bacterial metabolic adaptation during chronic infection. Inactivation of lasR also resulted in increased beta-lactamase activity that increased tolerance to ceftazidime, a widely used beta-lactam antibiotic. Loss of LasR function may represent a marker of an early stage in chronic infection of the CF airway with clinical implications for antibiotic resistance and disease progression.
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                Author and article information

                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group
                2045-2322
                28 January 2016
                2016
                : 6
                : 19906
                Affiliations
                [1 ]UMR 7266 CNRS- Littoral Environnement et Sociétés, Microbial Physiology Group - Université de La Rochelle, Avenue Michel Crépeau , 17042 La Rochelle, France
                [2 ]School of Physics, University of Exeter , Exeter EX4 4QL, United Kingdom
                [3 ]Laboratoire Mathématiques, Image et Applications EA 3165, Université de La Rochelle , France
                [4 ]Institut Français pour la Recherche et l’Exploitation de la Mer, Unité Santé Génétique et Microbiologie des Mollusques, Laboratoire de Génétique et de Pathologie des Mollusques Marins , La Tremblade, France
                [5 ]UMR 7283 CNRS Laboratoire de Chimie Bactérienne, Institut de Microbiologie de la Méditerranée, University of Aix-Marseille , Marseille, France
                Author notes
                [*]

                These authors contributed equally to this work.

                Article
                srep19906
                10.1038/srep19906
                4730217
                26819100
                b534013b-cdb3-4ab0-bb0a-320b626cbf93
                Copyright © 2016, Macmillan Publishers Limited

                This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

                History
                : 30 July 2015
                : 17 December 2015
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