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      Biofilms of a Bacillus subtilis Hospital Isolate Protect Staphylococcus aureus from Biocide Action

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          Abstract

          The development of a biofilm constitutes a survival strategy by providing bacteria a protective environment safe from stresses such as microbicide action and can thus lead to important health-care problems. In this study, biofilm resistance of a Bacillus subtilis strain (called hereafter ND medical) recently isolated from endoscope washer-disinfectors to peracetic acid was investigated and its ability to protect the pathogen Staphylococcus aureus in mixed biofilms was evaluated. Biocide action within Bacillus subtilis biofilms was visualised in real time using a non-invasive 4D confocal imaging method. The resistance of single species and mixed biofilms to peracetic acid was quantified using standard plate counting methods and their architecture was explored using confocal imaging and electronic microscopy. The results showed that the ND medical strain demonstrates the ability to make very large amount of biofilm together with hyper-resistance to the concentration of PAA used in many formulations (3500 ppm). Evidences strongly suggest that the enhanced resistance of the ND medical strain was related to the specific three-dimensional structure of the biofilm and the large amount of the extracellular matrix produced which can hinder the penetration of peracetic acid. When grown in mixed biofilm with Staphylococcus aureus, the ND medical strain demonstrated the ability to protect the pathogen from PAA action, thus enabling its persistence in the environment. This work points out the ability of bacteria to adapt to an extremely hostile environment, and the necessity of considering multi-organism ecosystems instead of single species model to decipher the mechanisms of biofilm resistance to antimicrobials agents.

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          Most cited references33

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          Fruiting body formation by Bacillus subtilis.

          Spore formation by the bacterium Bacillus subtilis has long been studied as a model for cellular differentiation, but predominantly as a single cell. When analyzed within the context of highly structured, surface-associated communities (biofilms), spore formation was discovered to have heretofore unsuspected spatial organization. Initially, motile cells differentiated into aligned chains of attached cells that eventually produced aerial structures, or fruiting bodies, that served as preferential sites for sporulation. Fruiting body formation depended on regulatory genes required early in sporulation and on genes evidently needed for exopolysaccharide and surfactin production. The formation of aerial structures was robust in natural isolates but not in laboratory strains, an indication that multicellularity has been lost during domestication of B. subtilis. Other microbial differentiation processes long thought to involve only single cells could display the spatial organization characteristic of multicellular organisms when studied with recent natural isolates.
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            Aminoglycoside antibiotics induce bacterial biofilm formation.

            Biofilms are adherent aggregates of bacterial cells that form on biotic and abiotic surfaces, including human tissues. Biofilms resist antibiotic treatment and contribute to bacterial persistence in chronic infections. Hence, the elucidation of the mechanisms by which biofilms are formed may assist in the treatment of chronic infections, such as Pseudomonas aeruginosa in the airways of patients with cystic fibrosis. Here we show that subinhibitory concentrations of aminoglycoside antibiotics induce biofilm formation in P. aeruginosa and Escherichia coli. In P. aeruginosa, a gene, which we designated aminoglycoside response regulator (arr), was essential for this induction and contributed to biofilm-specific aminoglycoside resistance. The arr gene is predicted to encode an inner-membrane phosphodiesterase whose substrate is cyclic di-guanosine monophosphate (c-di-GMP)-a bacterial second messenger that regulates cell surface adhesiveness. We found that membranes from arr mutants had diminished c-di-GMP phosphodiesterase activity, and P. aeruginosa cells with a mutation changing a predicted catalytic residue of Arr were defective in their biofilm response to tobramycin. Furthermore, tobramycin-inducible biofilm formation was inhibited by exogenous GTP, which is known to inhibit c-di-GMP phosphodiesterase activity. Our results demonstrate that biofilm formation can be a specific, defensive reaction to the presence of antibiotics, and indicate that the molecular basis of this response includes alterations in the level of c-di-GMP.
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              A major protein component of the Bacillus subtilis biofilm matrix.

              Microbes construct structurally complex multicellular communities (biofilms) through production of an extracellular matrix. Here we present evidence from scanning electron microscopy showing that a wild strain of the Gram positive bacterium Bacillus subtilis builds such a matrix. Genetic, biochemical and cytological evidence indicates that the matrix is composed predominantly of a protein component, TasA, and an exopolysaccharide component. The absence of TasA or the exopolysaccharide resulted in a residual matrix, while the absence of both components led to complete failure to form complex multicellular communities. Extracellular complementation experiments revealed that a functional matrix can be assembled even when TasA and the exopolysaccharide are produced by different cells, reinforcing the view that the components contribute to matrix formation in an extracellular manner. Having defined the major components of the biofilm matrix and the control of their synthesis by the global regulator SinR, we present a working model for how B. subtilis switches between nomadic and sedentary lifestyles.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2012
                4 September 2012
                : 7
                : 9
                : e44506
                Affiliations
                [1 ]INRA, UMR 1319 MICALIS, Jouy-en-Josas, France
                [2 ]AgroParisTech, UMR MICALIS, Jouy-en-Josas, France
                [3 ]CNRS, Jouy-en-Josas, France
                [4 ]Welsh School of Pharmacy, Cardiff University, Cardiff, United Kingdom
                [5 ]STERIS, Fontenay aux Roses, France
                Institut Pasteur, France
                Author notes

                Competing Interests: The authors have read the journal’s policy and have the following conflicts: V. Thomas, co-author of the paper, is employed by a commercial company, Steris SA (STERIS SA, 18, route du Panorama 92265 Fontenay-aux-Roses France +33-146548557 (phone), +33-146549843 (fax)). However, this does not alter the authors’ adherence to all the PLOS ONE policies on sharing data and materials.

                Conceived and designed the experiments: AB FDB VT RB. Performed the experiments: AB DLC TM MPSV RB. Analyzed the data: AB RB. Contributed reagents/materials/analysis tools: AB SA DL VT JYM RB. Wrote the paper: AB RB.

                Article
                PONE-D-12-06272
                10.1371/journal.pone.0044506
                3433435
                22973457
                87d08bec-cd3b-476c-bdca-623d7ec830d5
                Copyright @ 2012

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 2 March 2012
                : 6 August 2012
                Page count
                Pages: 9
                Funding
                This project was funded by the Medicen, Ile-de-France, competitiveness cluster and the National Institute for Agronomic Research. Financial support of the confopcal microscope was provided by the the Essonne department. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology
                Ecology
                Microbial Ecology
                Microbiology
                Bacteriology
                Bacterial Biofilms
                Applied Microbiology
                Bacterial Pathogens
                Medical Microbiology
                Microbial Control
                Microbial Growth and Development
                Microbial Pathogens
                Model Organisms
                Prokaryotic Models
                Bacillus Subtilis
                Medicine
                Diagnostic Medicine
                Pathology
                Clinical Pathology
                Clinical Microbiology
                Infectious Diseases
                Bacterial Diseases
                Staphylococcus Aureus
                Infectious Disease Control

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                Uncategorized

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