O-antigen protects gram-negative bacteria from histone killing
Beyond their traditional role of wrapping DNA, histones display antibacterial activity to Gram-negative and -positive bacteria. To identify bacterial components that allow survival to a histone challenge, we selected resistant bacteria from homologous Escherichia coli libraries that harbor plasmids...
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Published in | PloS one Vol. 8; no. 8; p. e71097 |
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Main Authors | , , , |
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Language | English |
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08.08.2013
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Abstract | Beyond their traditional role of wrapping DNA, histones display antibacterial activity to Gram-negative and -positive bacteria. To identify bacterial components that allow survival to a histone challenge, we selected resistant bacteria from homologous Escherichia coli libraries that harbor plasmids carrying pieces of the chromosome in different sizes. We identified genes required for exopolysaccharide production and for the synthesis of the polysaccharide domain of the lipopolysaccharide, called O-antigen. Indeed, O-antigen and exopolysaccharide conferred further resistance to histones. Notably, O-antigen also conferred resistance to histones in the pathogens Shigella flexneri and Klebsiella pneumoniae. |
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AbstractList | Beyond their traditional role of wrapping DNA, histones display antibacterial activity to Gram-negative and -positive bacteria. To identify bacterial components that allow survival to a histone challenge, we selected resistant bacteria from homologous
Escherichia coli
libraries that harbor plasmids carrying pieces of the chromosome in different sizes. We identified genes required for exopolysaccharide production and for the synthesis of the polysaccharide domain of the lipopolysaccharide, called O-antigen. Indeed, O-antigen and exopolysaccharide conferred further resistance to histones. Notably, O-antigen also conferred resistance to histones in the pathogens
Shigella flexneri
and
Klebsiella pneumoniae
. Beyond their traditional role of wrapping DNA, histones display antibacterial activity to Gram-negative and -positive bacteria. To identify bacterial components that allow survival to a histone challenge, we selected resistant bacteria from homologous Escherichia coli libraries that harbor plasmids carrying pieces of the chromosome in different sizes. We identified genes required for exopolysaccharide production and for the synthesis of the polysaccharide domain of the lipopolysaccharide, called O-antigen. Indeed, O-antigen and exopolysaccharide conferred further resistance to histones. Notably, O-antigen also conferred resistance to histones in the pathogens Shigella flexneri and Klebsiella pneumoniae. |
Audience | Academic |
Author | Chaput, Catherine Gill, Ryan T Zychlinsky, Arturo Spindler, Eileen |
AuthorAffiliation | 2 Department of Chemical and Biological Engineering, University of Colorado, Boulder, Colorado, United States of America 1 Department of Cellular Microbiology, Max-Planck Institute for Infection Biology, Berlin, Germany The Scripps Research Institute and Sorrento Therapeutics, Inc., United States of America |
AuthorAffiliation_xml | – name: 1 Department of Cellular Microbiology, Max-Planck Institute for Infection Biology, Berlin, Germany – name: 2 Department of Chemical and Biological Engineering, University of Colorado, Boulder, Colorado, United States of America – name: The Scripps Research Institute and Sorrento Therapeutics, Inc., United States of America |
Author_xml | – sequence: 1 givenname: Catherine surname: Chaput fullname: Chaput, Catherine email: catherine.chaput@charite.de organization: Department of Cellular Microbiology, Max-Planck Institute for Infection Biology, Berlin, Germany. catherine.chaput@charite.de – sequence: 2 givenname: Eileen surname: Spindler fullname: Spindler, Eileen – sequence: 3 givenname: Ryan T surname: Gill fullname: Gill, Ryan T – sequence: 4 givenname: Arturo surname: Zychlinsky fullname: Zychlinsky, Arturo |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/23951089$$D View this record in MEDLINE/PubMed |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Current address: Department of Infectious Diseases and Pulmonary Medicine, Charité University Hospital, Berlin, Germany Competing Interests: The authors have declared that no competing interests exist. Conceived and designed the experiments: CC RTG AZ. Performed the experiments: CC ES. Analyzed the data: CC. Contributed reagents/materials/analysis tools: CC ES RTG. Wrote the paper: CC. Current address: Opxbio, Boulder, Colorado, United States of America |
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SubjectTerms | Antibacterial activity Antigens Antimicrobial agents Bacteria Bacterial Proteins - genetics Bacterial Proteins - metabolism Bioengineering Biology Data analysis Deoxyribonucleic acid DNA DNA binding proteins E coli Escherichia coli Escherichia coli - physiology Gene Expression Regulation, Bacterial Genes, Bacterial Gram-negative bacteria Gram-Negative Bacterial Infections - metabolism Gram-Negative Bacterial Infections - microbiology Histones Histones - metabolism Homology Host-Pathogen Interactions Humans Klebsiella Klebsiella pneumoniae Klebsiella pneumoniae - physiology Lipopolysaccharides Medical screening Microbial drug resistance Mitogens Neutrophils O Antigens - genetics O Antigens - metabolism Peptides Plasmids Polysaccharides Polysaccharides - genetics Polysaccharides - metabolism Shigella Shigella flexneri - physiology Signal Transduction Staphylococcus aureus |
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Title | O-antigen protects gram-negative bacteria from histone killing |
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