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      High‐throughput transposon sequencing highlights the cell wall as an important barrier for osmotic stress in methicillin resistant Staphylococcus aureus and underlines a tailored response to different osmotic stressors

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          Abstract

          Staphylococcus aureus is an opportunistic pathogen that can cause soft tissue infections but is also a frequent cause of foodborne illnesses. One contributing factor for this food association is its high salt tolerance allowing this organism to survive commonly used food preservation methods. How this resistance is mediated is poorly understood, particularly during long‐term exposure. In this study, we used transposon sequencing (TN‐seq) to understand how the responses to osmotic stressors differ. Our results revealed distinctly different long‐term responses to NaCl, KCl and sucrose stresses. In addition, we identified the DUF2538 domain containing gene SAUSA300_0957 (gene 957) as essential under salt stress. Interestingly, a 957 mutant was less susceptible to oxacillin and showed increased peptidoglycan crosslinking. The salt sensitivity phenotype could be suppressed by amino acid substitutions in the transglycosylase domain of the penicillin‐binding protein Pbp2, and these changes restored the peptidoglycan crosslinking to WT levels. These results indicate that increased crosslinking of the peptidoglycan polymer can be detrimental and highlight a critical role of the bacterial cell wall for osmotic stress resistance. This study will serve as a starting point for future research on osmotic stress response and help develop better strategies to tackle foodborne staphylococcal infections.

          Abstract

          Staphylococcus aureus is able to grow in the presence of high concentrations of NaCl but the exact genetic factors contributing to this are unknown. Using a high‐throughput TN‐seq approach, we identified gene 957 as an important factor for the salt stress resistance in S. aureus. A 957‐mutant was not only salt sensitive but also showed increased peptidoglycan crosslinking, altogether highlighting the cell wall as an important barrier against osmotic stress.

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          Most cited references73

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          Peptidoglycan structure and architecture.

          The peptidoglycan (murein) sacculus is a unique and essential structural element in the cell wall of most bacteria. Made of glycan strands cross-linked by short peptides, the sacculus forms a closed, bag-shaped structure surrounding the cytoplasmic membrane. There is a high diversity in the composition and sequence of the peptides in the peptidoglycan from different species. Furthermore, in several species examined, the fine structure of the peptidoglycan significantly varies with the growth conditions. Limited number of biophysical data on the thickness, elasticity and porosity of peptidoglycan are available. The different models for the architecture of peptidoglycan are discussed with respect to structural and physical parameters.
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            A Genetic Resource for Rapid and Comprehensive Phenotype Screening of Nonessential Staphylococcus aureus Genes

            ABSTRACT To enhance the research capabilities of investigators interested in Staphylococcus aureus, the Nebraska Center for Staphylococcal Research (CSR) has generated a sequence-defined transposon mutant library consisting of 1,952 strains, each containing a single mutation within a nonessential gene of the epidemic community-associated methicillin-resistant S. aureus (CA-MRSA) isolate USA300. To demonstrate the utility of this library for large-scale screening of phenotypic alterations, we spotted the library on indicator plates to assess hemolytic potential, protease production, pigmentation, and mannitol utilization. As expected, we identified many genes known to function in these processes, thus validating the utility of this approach. Importantly, we also identified genes not previously associated with these phenotypes. In total, 71 mutants displayed differential hemolysis activities, the majority of which were not previously known to influence hemolysin production. Furthermore, 62 mutants were defective in protease activity, with only 14 previously demonstrated to be involved in the production of extracellular proteases. In addition, 38 mutations affected pigment formation, while only 7 influenced mannitol fermentation, underscoring the sensitivity of this approach to identify rare phenotypes. Finally, 579 open reading frames were not interrupted by a transposon, thus providing potentially new essential gene targets for subsequent antibacterial discovery. Overall, the Nebraska Transposon Mutant Library represents a valuable new resource for the research community that should greatly enhance investigations of this important human pathogen.
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              Wall teichoic acids of gram-positive bacteria.

              The peptidoglycan layers of many gram-positive bacteria are densely functionalized with anionic glycopolymers known as wall teichoic acids (WTAs). These polymers play crucial roles in cell shape determination, regulation of cell division, and other fundamental aspects of gram-positive bacterial physiology. Additionally, WTAs are important in pathogenesis and play key roles in antibiotic resistance. We provide an overview of WTA structure and biosynthesis, review recent studies on the biological roles of these polymers, and highlight remaining questions. We also discuss prospects for exploiting WTA biosynthesis as a target for new therapies to overcome resistant infections.
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                Author and article information

                Contributors
                a.grundling@imperial.ac.uk
                Journal
                Mol Microbiol
                Mol. Microbiol
                10.1111/(ISSN)1365-2958
                MMI
                Molecular Microbiology
                John Wiley and Sons Inc. (Hoboken )
                0950-382X
                1365-2958
                16 December 2019
                April 2020
                : 113
                : 4 ( doiID: 10.1111/mmi.v113.4 )
                : 699-717
                Affiliations
                [ 1 ] Section of Molecular Microbiology and MRC Centre for Molecular Bacteriology and Infection Imperial College London London UK
                [ 2 ] Department of Microbiology and Immunobiology Harvard Medical School Boston MA USA
                [ 3 ]Present address: Section of Respiratory Infections National Heart and Lung Institute, Imperial College London London UK
                Author notes
                [*] [* ] Correspondence

                Angelika Gründling, Section of Molecular Microbiology and MRC Centre for Molecular Bacteriology and Infection, Imperial College London, London, SW7 2AZ, UK.

                Email: a.grundling@ 123456imperial.ac.uk

                Author information
                https://orcid.org/0000-0002-4566-7226
                https://orcid.org/0000-0001-6961-0980
                https://orcid.org/0000-0003-4585-319X
                https://orcid.org/0000-0002-5446-3452
                https://orcid.org/0000-0002-0545-914X
                https://orcid.org/0000-0002-6235-8687
                Article
                MMI14433
                10.1111/mmi.14433
                7176532
                31770461
                b6f6f24b-4d94-4e48-a0e6-beb20780a579
                © 2019 The Authors. Molecular Microbiology published by John Wiley & Sons Ltd

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 22 November 2019
                : 24 November 2019
                Page count
                Figures: 8, Tables: 0, Pages: 26, Words: 30121
                Funding
                Funded by: National Institutes of Health , open-funder-registry 10.13039/100000002;
                Award ID: P01AI083214
                Funded by: Deutsche Forschungsgemeinschaft , open-funder-registry 10.13039/501100001659;
                Award ID: SCHU 3159/1–1
                Funded by: Wellcome Trust , open-funder-registry 10.13039/100004440;
                Award ID: 100289 and 210671/Z/18/Z
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                April 2020
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.8.1 mode:remove_FC converted:12.05.2020

                Microbiology & Virology
                duf25380,kcl,nacl,osmotic stress,pbp2,sucrose,s. aureus
                Microbiology & Virology
                duf25380, kcl, nacl, osmotic stress, pbp2, sucrose, s. aureus

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