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      Growth of Mycobacterium tuberculosis biofilms containing free mycolic acids and harbouring drug-tolerant bacteria

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          Abstract

          Successful treatment of human tuberculosis requires 6–9 months' therapy with multiple antibiotics. Incomplete clearance of tubercle bacilli frequently results in disease relapse, presumably as a result of reactivation of persistent drug-tolerant Mycobacterium tuberculosis cells, although the nature and location of these persisters are not known. In other pathogens, antibiotic tolerance is often associated with the formation of biofilms – organized communities of surface-attached cells – but physiologically and genetically defined M. tuberculosis biofilms have not been described. Here, we show that M. tuberculosis forms biofilms with specific environmental and genetic requirements distinct from those for planktonic growth, which contain an extracellular matrix rich in free mycolic acids, and harbour an important drug-tolerant population that persist despite exposure to high levels of antibiotics.

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          Most cited references40

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          Bacterial persistence as a phenotypic switch.

          A fraction of a genetically homogeneous microbial population may survive exposure to stress such as antibiotic treatment. Unlike resistant mutants, cells regrown from such persistent bacteria remain sensitive to the antibiotic. We investigated the persistence of single cells of Escherichia coli with the use of microfluidic devices. Persistence was linked to preexisting heterogeneity in bacterial populations because phenotypic switching occurred between normally growing cells and persister cells having reduced growth rates. Quantitative measurements led to a simple mathematical description of the persistence switch. Inherent heterogeneity of bacterial populations may be important in adaptation to fluctuating environments and in the persistence of bacterial infections.
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            Persister cells, dormancy and infectious disease.

            Kim Lewis (2007)
            Several well-recognized puzzles in microbiology have remained unsolved for decades. These include latent bacterial infections, unculturable microorganisms, persister cells and biofilm multidrug tolerance. Accumulating evidence suggests that these seemingly disparate phenomena result from the ability of bacteria to enter into a dormant (non-dividing) state. The molecular mechanisms that underlie the formation of dormant persister cells are now being unravelled and are the focus of this Review.
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              Biofilms: the matrix revisited.

              Microbes often construct and live within surface-associated multicellular communities known as biofilms. The precise structure, chemistry and physiology of the biofilm all vary with the nature of its resident microbes and local environment. However, an important commonality among biofilms is that their structural integrity critically depends upon an extracellular matrix produced by their constituent cells. Extracellular matrices might be as diverse as biofilms, and they contribute significantly to the organization of the community. This review discusses recent advances in our understanding of the extracellular matrix and its role in biofilm biology.
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                Author and article information

                Journal
                Mol Microbiol
                mmi
                Molecular Microbiology
                Blackwell Publishing Ltd
                0950-382X
                1365-2958
                July 2008
                27 May 2008
                : 69
                : 1
                : 164-174
                Affiliations
                [1 ]Department of Biological Sciences, University of Pittsburgh Pittsburgh, PA 15260, USA
                [2 ]Howard Hughes Medical Institute, Department of Microbiology and Immunology, Albert Einstein College of Medicine 1300 Morris Park Avenue, Bronx, NY 10461, USA
                [3 ]Unité de Glycobiologie Structurale et Fonctionnelle, CNRS UMR 8576, Université des Sciences et Technologies de Lille 59650 Villeneuve d'Ascq, Cédex, France
                [4 ]Laboratoire de Dynamique des Interactions Membranaires Normales et Pathologiques, Université de Montpellier II et I, CNRS UMR 5235, case 107, Place Eugène Bataillon, 34095 Montpellier Cedex 05, France
                [5 ]INSERM, DIMNP, Place Eugène Bataillon 34095 Montpellier Cedex 05, France
                Author notes
                *For correspondence. E-mail: gfh@ 123456pitt.edu ; Tel. 412 624 4350; Fax 412 624 9311.
                Article
                10.1111/j.1365-2958.2008.06274.x
                2615189
                18466296
                7caabe57-d524-4164-b51f-50ef2c281c0a
                © 2008 The Authors Journal compilation © 2008 Blackwell Publishing Ltd

                Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.

                History
                : 23 April 2008
                Categories
                Research Articles

                Microbiology & Virology
                Microbiology & Virology

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