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      The staphylococcal exopolysaccharide PIA – Biosynthesis and role in biofilm formation, colonization, and infection

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          Highlights

          • PIA is a key extracellular matrix component in staphylococci and other bacteria.

          • PIA is a cationic, partially deacetylated N-acetylglucosamine polymer.

          • PIA has a major role in bacterial biofilms and biofilm-associated infection.

          Abstract

          Exopolysaccharide is a key part of the extracellular matrix that contributes to important mechanisms of bacterial pathogenicity, most notably biofilm formation and immune evasion. In the human pathogens Staphylococcus aureus and S. epidermidis, as well as in many other staphylococcal species, the only exopolysaccharide is polysaccharide intercellular adhesin (PIA), a cationic, partially deacetylated homopolymer of N-acetylglucosamine, whose biosynthetic machinery is encoded in the ica locus. PIA production is strongly dependent on environmental conditions and controlled by many regulatory systems. PIA contributes significantly to staphylococcal biofilm formation and immune evasion mechanisms, such as resistance to antimicrobial peptides and ingestion and killing by phagocytes, and presence of the ica genes is associated with infectivity. Due to its role in pathogenesis, PIA has raised considerable interest as a potential vaccine component or target.

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          Most cited references210

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          <i>Staphylococcus aureus</i> Infections

          New England Journal of Medicine, 339(8), 520-532
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            Molecular mechanisms of biofilm-based antibiotic resistance and tolerance in pathogenic bacteria.

            Biofilms are surface-attached groups of microbial cells encased in an extracellular matrix that are significantly less susceptible to antimicrobial agents than non-adherent, planktonic cells. Biofilm-based infections are, as a result, extremely difficult to cure. A wide range of molecular mechanisms contribute to the high degree of recalcitrance that is characteristic of biofilm communities. These mechanisms include, among others, interaction of antimicrobials with biofilm matrix components, reduced growth rates and the various actions of specific genetic determinants of antibiotic resistance and tolerance. Alone, each of these mechanisms only partially accounts for the increased antimicrobial recalcitrance observed in biofilms. Acting in concert, however, these defences help to ensure the survival of biofilm cells in the face of even the most aggressive antimicrobial treatment regimens. This review summarises both historical and recent scientific data in support of the known biofilm resistance and tolerance mechanisms. Additionally, suggestions for future work in the field are provided.
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              The skin microbiome

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                Author and article information

                Contributors
                Journal
                Comput Struct Biotechnol J
                Comput Struct Biotechnol J
                Computational and Structural Biotechnology Journal
                Research Network of Computational and Structural Biotechnology
                2001-0370
                04 November 2020
                2020
                04 November 2020
                : 18
                : 3324-3334
                Affiliations
                [a ]Pathogen Molecular Genetics Section, Laboratory of Bacteriology, National Institute of Allergy and Infectious Diseases, U.S. National Institutes of Health, 50 South Drive, Bethesda 20814, MD, USA
                [b ]School of Biotechnology, International University, Vietnam National University of Ho Chi Minh City, Khu Pho 6, Thu Duc, Ho Chi Minh City, Viet Nam
                Author notes
                [* ]Corresponding author. motto@ 123456niaid.nih.gov
                Article
                S2001-0370(20)30449-9
                10.1016/j.csbj.2020.10.027
                7674160
                33240473
                602be3e3-1d9e-4ca4-a4cd-9517584907c3

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 12 August 2020
                : 23 October 2020
                : 25 October 2020
                Categories
                Review

                cons, coagulase-negative staphylococci,pia, polysaccharide intercellular adhesin,pnag, poly-n-acetylglucosamine,mrsa, methicillin-resistant staphylococcus aureus,mssa, methicillin-sensitive staphylococcus aureus,poly-n-acetylglucosamine,pnag,pia,biofilm,colonization,polysaccharide intercellular adhesin,staphylococcus epidermidis,staphylococcus aureus,device-related infection

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