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      Lipopolysaccharide modification in Gram-negative bacteria during chronic infection

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          Abstract

          The Gram-negative bacterial lipopolysaccharide (LPS) is a major component of the outer membrane that plays a key role in host–pathogen interactions with the innate immune system. During infection, bacteria are exposed to a host environment that is typically dominated by inflammatory cells and soluble factors, including antibiotics, which provide cues about regulation of gene expression. Bacterial adaptive changes including modulation of LPS synthesis and structure are a conserved theme in infections, irrespective of the type or bacteria or the site of infection. In general, these changes result in immune system evasion, persisting inflammation and increased antimicrobial resistance. Here, we review the modifications of LPS structure and biosynthetic pathways that occur upon adaptation of model opportunistic pathogens ( Pseudomonas aeruginosa, Burkholderia cepacia complex bacteria, Helicobacter pylori and Salmonella enterica) to chronic infection in respiratory and gastrointestinal sites. We also discuss the molecular mechanisms of these variations and their role in the host–pathogen interaction.

          Abstract

          The authors review modifications of lipopolysaccharide structure and biosynthetic pathways that occur upon bacterial adaptation to chronic respiratory and gastrointestinal infections.

          Abstract

          Graphical Abstract Figure.

          The authors review modifications of lipopolysaccharide structure and biosynthetic pathways that occur upon bacterial adaptation to chronic respiratory and gastrointestinal infections.

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          Author and article information

          Journal
          FEMS Microbiol Rev
          FEMS Microbiol. Rev
          femsre
          femsre
          FEMS Microbiology Reviews
          Oxford University Press
          0168-6445
          1574-6976
          12 April 2016
          July 2016
          : 40
          : 4
          : 480-493
          Affiliations
          [1 ]Institute for Bioengineering and Biosciences, Department of Bioengineering, Instituto Superior Técnico, Universidade de Lisboa, Lisbon 1049-001, Portugal
          [2 ]Department of Microbiology and Immunology, University of Western Ontario, London, ON N6A 5C1, Canada
          [3 ]Centre for Infection and Immunity, Queen's University Belfast, Belfast BT9 7BL, UK
          Author notes
          [* ] Corresponding author: Centre for Infection and Immunity, Queen's University Belfast, 97 Lisburn Rd, Belfast BT9 7BL, UK. Tel: +44-28-9097-6025; E-mail: m.valvano@ 123456qub.ac.uk
          Article
          PMC4931227 PMC4931227 4931227
          10.1093/femsre/fuw007
          4931227
          27075488
          21004846-3c69-4ac9-9a7b-f620cf73fb7f
          © FEMS 2016. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com
          History
          : 10 March 2016
          : 23 August 2015
          Page count
          Pages: 14
          Categories
          Review Article
          Custom metadata
          July 2016

          gastric ulcer, Helicobacter pylori ,cystic fibrosis, Burkholderia cenocepacia , Pseudomonas aeruginosa ,lipid A,O antigen,adaptive mutation

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