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Cationic antimicrobial peptides promote microbial mutagenesis and pathoadaptation in chronic infections PLoS Pathog 10 e Helicobacter pylori genomic microevolution during naturally occurring transmission between adults PLoS One 8 e Cystic fibrosis-niche adaptation of Pseudomonas aeruginosa reduces virulence in multiple infection hosts PLoS One 7 e Proteomic profiling of Burkholderia cenocepacia clonal isolates with different virulence potential retrieved from a cystic fibrosis patient during chronic lung infection PLoS One 8 e Quantitative proteomics 2-D DIGE reveals molecular strategies employed by Burkholderia cenocepacia to adapt to the airways of cystic fibrosis patients under antimicrobial therapy Proteomics 11 Helicobacter pylori : friend or foe?

World J Gastroenterol 20 Google Preview. Lewis X biosynthesis in Helicobacter pylori. Mucoid conversion of Pseudomonas aeruginosa by hydrogen peroxide: a mechanism for virulence activation in the cystic fibrosis lung Microbiology Lipid A in Helicobacter pylori Infect Immun 60 7. Lipopolysaccharide transport to the cell surface: periplasmic transport and assembly into the outer membrane Philos Trans R Soc B PhoQ mutations promote lipid A modification and polymyxin resistance of Pseudomonas aeruginosa found in colistin-treated cystic fibrosis patients Antimicrob Agents Ch 55 9.

Genomic expression analysis reveals strategies of Burkholderia cenocepacia to adapt to cystic fibrosis patients' airways and antimicrobial therapy PLoS One 6 e Simultaneous expression of type 1 and type 2 Lewis blood group antigens by Helicobacter pylori lipopolysaccharides.

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Microevolution of Helicobacter pylori during prolonged infection of single hosts and within families PLoS Genet 6 e Pseudomonas aeruginosa population diversity and turnover in cystic fibrosis chronic infections Am J Resp Crit Care 9.

MutS deficiency and activity of the error-prone DNA polymerase IV are crucial for determining mucA as the main target for mucoid conversion in Pseudomonas aeruginosa Mol Microbiol 64 Low biological activity of Helicobacter pylori lipopolysaccharide Infect Immun 60 6.

Antigenic mimicry between Helicobacter pylori and gastric mucosa in the pathogenesis of body atrophic gastritis Gastroenterology Lipopolysaccharide diversity evolving in Helicobacter pylori communities through genetic modifications in fucosyltransferases PLoS One 3 e Extracellular zinc induces phosphoethanolamine addition to Pseudomonas aeruginosa lipid A via the ColRS two-component system Mol Microbiol 97 Metabolic network analysis of Pseudomonas aeruginosa during chronic cystic fibrosis lung infection J Bacteriol High frequency of hypermutable Pseudomonas aeruginosa in cystic fibrosis lung infection Science 4.

Establishment of systemic Brucella melitensis infection through the digestive tract requires urease, the type IV secretion system, and lipopolysaccharide O antigen Infect Immun 77 Structure elucidation of the O-Antigen of Salmonella enterica O51 and its structural and genetic relation to the O-Antigen of Escherichia coli O23 Biochemistry 76 9. Activation of human THP-1 cells and rat bone marrow-derived macrophages by Helicobacter pylori lipopolysaccharide Infect Immun 63 7.

Posselt G Backert S Wessler S The functional interplay of Helicobacter pylori factors with gastric epithelial cells induces a multi-step process in pathogenesis Cell Commun Signal 11 Lipid A modification systems in gram-negative bacteria Annu Rev Biochem 76 Lewis antigen expression and stability in Helicobacter pylori isolated from serial gastric biopsies J Infect Dis Bacterial polysaccharide synthesis and gene nomenclature Trends Microbiol 4 The WaaL O-antigen lipopolysaccharide ligase has features in common with metal ion-independent inverting glycosyltransferases Glycobiology 22 Structural characterization of the outer core and the O-chain linkage region of lipopolysaccharide from Pseudomonas aeruginosa serotype O5 Eur J Biochem Localization of Burkholderia cepacia complex bacteria in cystic fibrosis lungs and interactions with Pseudomonas aeruginosa in hypoxic mucus Infect Immun 82 Effect of Helicobacter pylori lipopolysaccharide LPS and LPS derivatives on the production of tissue factor and plasminogen activator inhibitor type 2 by human blood mononuclear cells J Infect Dis Complete structural characterization of the lipid A fraction of a clinical strain of B.

The complete structure and pro-inflammatory activity of the lipooligosaccharide of the highly epidemic and virulent Gram-negative bacterium Burkholderia cenocepacia ET strain J Chemistry 13 Lipopolysaccharide transport to the cell surface: biosynthesis and extraction from the inner membrane Philos Trans R Soc B A changing gastric environment leads to adaptation of lipopolysaccharide variants in Helicobacter pylori populations during colonization PLoS One 4 e New insights into the Lpt machinery for lipopolysaccharide transport to the cell surface: LptA-LptC interaction and LptA stability as sensors of a properly assembled transenvelope complex J Bacteriol Microcolony formation: a novel biofilm model of Pseudomonas aeruginosa for the cystic fibrosis lung J Med Microbiol 54 Deciphering the unusual acylation pattern of Helicobacter pylori lipid A J Bacteriol Removal of the outer Kdo from Helicobacter pylori lipopolysaccharide and its impact on the bacterial surface Mol Microbiol 78 A divergent Pseudomonas aeruginosa palmitoyltransferase essential for cystic fibrosis-specific lipid A Mol Microbiol 91 Periplasmic cleavage and modification of the 1-phosphate group of Helicobacter pylori lipid A J Biol Chem The lipid A 1-phosphatase of Helicobacter pylori is required for resistance to the antimicrobial peptide polymyxin J Bacteriol Outbreak of Achromobacter xylosoxidans in an italian cystic fibrosis center: genome variability, biofilm production, antibiotic resistance, and motility in isolated strains Front Microbiol 5 Identification of specific and universal virulence factors in Burkholderia cenocepacia strains by using multiple infection hosts Infect Immun 77 Valvano MA Common themes in glycoconjugate assembly using the biogenesis of O-antigen lipopolysaccharide as a model system Biochemistry 76 Molecular Medical Microbiology Vol.

Valvano MA Messner P Kosma P Novel pathways for biosynthesis of nucleotide-activated glycero-manno-heptose precursors of bacterial glycoproteins and cell surface polysaccharides Microbiology Variable number of tandem repeats in clinical strains of Haemophilus influenzae Infect Immun 65 Adaptation of Stenotrophomonas maltophilia in cystic fibrosis: molecular diversity, mutation frequency and antibiotic resistance Int J Med Microbiol 9. Lipopolysaccharide core phosphates are required for viability and intrinsic drug resistance in Pseudomonas aeruginosa Mol Microbiol 35 Lewis antigens in Helicobacter pylori : biosynthesis and phase variation Mol Microbiol 36 Genotypic and phenotypic variation in Pseudomonas aeruginosa reveals signatures of secondary infection and mutator activity in certain cystic fibrosis patients with chronic lung infections Infect Immun 79 Comparative phylogenomics and evolution of the Brucellae reveal a path to virulence J Bacteriol WHO Schistosomes, liver flukes and Helicobacter pylori.

O-antigen diversity and lateral transfer of the wbe region among Vibrio splendidus isolates Environ Microbiol 12 Mucoid and nonmucoid Burkholderia cepacia complex bacteria in cystic fibrosis infections Am J Resp Crit Care 67 Swimming motility in a longitudinal collection of clinical isolates of Burkholderia cepacia complex bacteria from people with cystic fibrosis PLoS One 9 e Oxford University Press is a department of the University of Oxford.

It furthers the University's objective of excellence in research, scholarship, and education by publishing worldwide. Sign In or Create an Account. Sign In. Advanced Search. Search Menu. Article Navigation. Close mobile search navigation Article Navigation. Volume Lipopolysaccharide modification in Gram-negative bacteria during chronic infection.

Maldonado , Rita F. Oxford Academic. Miguel A. Revision received:. Cite Cite Rita F. Select Format Select format. Permissions Icon Permissions. Open in new tab Download slide. Table 1. LPS genes altered in P. LPS metabolism. Lipid A biosynthesis and modification lpxO2 Cramer et al. Open in new tab. Table 2. Homologous gene in. Gene or locus. Infection with transmissible strains of Pseudomonas aeruginosa and clinical outcomes in adults with cystic fibrosis. Google Scholar Crossref. Search ADS.

Functional characterization of WaaL, a ligase associated with linking O-antigen polysaccharide to the core of Pseudomonas aeruginosa lipopolysaccharide. Microevolution of Helicobacter pylori type IV secretion systems in an ulcer disease patient over a ten-year period. Evidence of interspecies O antigen gene cluster transfer between Shigella boydii 15 and Escherichia fergusonii. Genetic interaction maps in Escherichia coli reveal functional crosstalk among cell envelope biogenesis pathways.

Molecular structures that influence the immunomodulatory properties of the lipid A and inner core region oligosaccharides of bacterial lipopolysaccharides. Google Scholar PubMed. The Helicobacter pylori genome sequence: genetic factors for long life in the gastric mucosa. Effect of a waaL mutation on lipopolysaccharide composition, oxidative stress survival, and virulence in Erwinia amylovora.

PBP3 inhibition elicits adaptive responses in Pseudomonas aeruginosa. Surface swarming motility by Pectobacterium atrosepticum is a latent phenotype that requires O antigen and is regulated by quorum sensing.

Sequence diversity of the mucABD locus in Pseudomonas aeruginosa isolates from patients with cystic fibrosis. Structures of the core oligosaccharide and O-units in the R- and SR-type lipopolysaccharides of reference strains of Pseudomonas aeruginosa O-serogroups.

Structural modifications of Helicobacter pylori lipopolysaccharide: an idea for how to live in peace. Dioxygenases in Burkholderia ambifaria and Yersinia pestis that hydroxylate the outer Kdo unit of lipopolysaccharide. Pseudomonas aeruginosa exploits lipid A and muropeptides modification as a strategy to lower innate immunity during cystic fibrosis lung infection. Antimicrobial resistance, respiratory tract infections and role of biofilms in lung infections in cystic fibrosis patients.

Long-term colonization of the cystic fibrosis lung by Burkholderia cepacia complex bacteria: epidemiology, clonal variation, and genome-wide expression alterations. Microevolution of the major common Pseudomonas aeruginosa clones C and PA14 in cystic fibrosis lungs. Helicobacter pylori versus the host: remodeling of the bacterial outer membrane is required for survival in the gastric mucosa.

The Yersinia kristensenii O11 O-antigen gene cluster was acquired by lateral gene transfer and incorporated at a novel chromosomal locus. Growth phenotypes of Pseudomonas aeruginosa lasR mutants adapted to the airways of cystic fibrosis patients. Ability of bacteria associated with chronic inflammatory disease to stimulate E-selectin expression and promote neutrophil adhesion.

Evolutionary genomics of epidemic and nonepidemic strains of Pseudomonas aeruginosa. Di Lorenzo. Myeloid differentiation factor 2 MD-2 by hypoacylated lipopolysaccharide from a clinical isolate of Burkholderia cenocepacia. Persistent cystic fibrosis isolate Pseudomonas aeruginosa strain RP73 exhibits an under-acylated LPS structure responsible of its low inflammatory activity.

Burkholderia cenocepacia in cystic fibrosis: epidemiology and molecular mechanisms of virulence. Evolutionary origins and sequence of the Escherichia coli O4 O-antigen gene cluster. O-antigen delays lipopolysaccharide recognition and impairs antibacterial host defense in murine intestinal epithelial cells. The Pseudomonas aeruginosa lipid A deacylase: selection for expression and loss within the cystic fibrosis airway.

Pseudomonas aeruginosa lipid A diversity and its recognition by Toll-like receptor 4. Unique lipid a modifications in Pseudomonas aeruginosa isolated from the airways of patients with cystic fibrosis. Antigastric autoantibodies in Helicobacter pylori infection: implications of histological and clinical parameters of gastritis. Recombination and mutation during long-term gastric colonization by Helicobacter pylori : estimates of clock rates, recombination size, and minimal age.

Dissemination of lipid A deacylases pagL among Gram-negative bacteria: identification of active-site histidine and serine residues. Lateral gene transfer of O1 serogroup encoding genes of Vibrio cholerae. Microbial pathogenesis in cystic fibrosis: mucoid Pseudomonas aeruginosa and Burkholderia cepacia.

Synthesis of lipopolysaccharide O-antigens by ABC transporter-dependent pathways. Pseudomonas aeruginosa isolates from patients with cystic fibrosis: a class of serum-sensitive, nontypable strains deficient in lipopolysaccharide O side chains. Five new genes are important for common polysaccharide antigen biosynthesis in Pseudomonas aeruginosa. Helicobacter pylori CagA and gastric cancer: a paradigm for hit-and-run carcinogenesis. Clinical significance of microbial infection and adaptation in cystic fibrosis.

Pseudomonas aeruginosa lasR mutants are associated with cystic fibrosis lung disease progression. Adaptation of Pseudomonas aeruginosa during persistence in the cystic fibrosis lung. Structural and genetic evidence for the close relationship between Escherichia coli O71 and Salmonella enterica O28 O-antigens. Helicobacter pylori lipopolysaccharide is synthesized via a novel pathway with an evolutionary connection to protein N -glycosylation.

Helicobacter pylori genetic diversity within the gastric niche of a single human host. Type III secretion phenotypes of Pseudomonas aeruginosa strains change during infection of individuals with cystic fibrosis. Interaction of gentamicin with the A band and B band lipopolysaccharides of Pseudomonas aeruginosa and its possible lethal effect.

Bacterial populations as perfect gases: genomic integrity and diversification tensions in Helicobacter pylori. A novel pathway for O-polysaccharide biosynthesis in Salmonella enterica serovar Borreze. Review: Lipopolysaccharide biosynthesis in Pseudomonas aeruginosa. Conserved and variable structural features in the lipopolysaccharide of Pseudomonas aeruginosa. Impact of large chromosomal inversions on the adaptation and evolution of Pseudomonas aeruginosa chronically colonizing cystic fibrosis lungs.

Genetic and Functional Diversity of Pseudomonas aeruginosa Lipopolysaccharide. Heterogeneity of biofilms formed by nonmucoid Pseudomonas aeruginosa isolates from patients with cystic fibrosis. Parallel bacterial evolution within multiple patients identifies candidate pathogenicity genes.

Cationic antimicrobial peptides promote microbial mutagenesis and pathoadaptation in chronic infections. Helicobacter pylori genomic microevolution during naturally occurring transmission between adults. Interactions of bacterial adhesins with extracellular matrix and plasma proteins: pathogenic implications and therapeutic possibilities. Cystic fibrosis-niche adaptation of Pseudomonas aeruginosa reduces virulence in multiple infection hosts. A decade of Burkholderia cenocepacia virulence determinant research.

Role of structural variations of polysaccharide antigens in the pathogenicity of Gram-negative bacteria. Proteomic profiling of Burkholderia cenocepacia clonal isolates with different virulence potential retrieved from a cystic fibrosis patient during chronic lung infection. Data collected with the food records were used in the multivariable models to study the association between dietary intake, at the level of energy and macronutrient intake, and serum LPS activity.

In the current LPS-diet analyses, data from individuals who completed the record for a minimum of three days were included. From the food record entries, data on all food items for which an unambiguous match was found in the diet questionnaire were extracted for subsequent analyses.

For example, the numbers of cups of coffee, reported in the food record, were calculated and divided by the number of days the record was kept six to obtain the average of daily cups of coffee consumed. These values were then compared with the entries made in the diet questionnaires. Similarly, for the food record entries of fish dishes, meat dishes, poultry, and so on the items listed in the FFQ part of the diet questionnaire , a daily average consumption frequency was calculated.

Based on these calculated consumption frequencies, each food group was recoded according to the seven-point scale of the FFQ part of the diet questionnaire, to allow the comparison between the two methods.

The respective statistical comparisons were performed using Chi squared test, Mann-Whitney U-test, and t-test. Exploratory factor analysis maximal likelihood and varimax rotation was conducted to reveal underlying constructs within the FFQ in both the LPS-diet study and the validation study.

The factor score was the sum of the scores for all items associated with that particular factor multiplied by its corresponding factor loading. In the validation study, the factor analysis was additionally conducted for the 6-day food record data. Within each dietary pattern, for which we could identify a reasonable match between the FFQ and the food record derived patterns, quartiles were formed based on the factor scores.

The proportion of individuals classified into the same quartile, the same or adjacent quartile, or opposite quartile by the FFQ and the food record, was calculated. The Spearman correlation coefficient was used to calculate the correlation between the factor scores of the matched dietary patterns in the validation study.

Moreover, it was used to explore the correlations between serum LPS activity and dietary variables both the factor scores of the FFQ-derived dietary patterns, and the energy, macronutrient, and fibre intake calculated from the food records. The independent associations between these dietary variables, and serum LPS activity were investigated in a multivariable generalized linear model. Multivariable nutrient density substitution model was used to examine the associations between macronutrient intakes and LPS activity, as previously described However one of the macronutrients, in each analysis, was left out.

Full models were corrected for sample storage time as the LPS activity may reduce with increasing sample storage time , age, sex, smoking, physical activity, and diabetic nephropathy status. The substitution models with fatty acid intake were additionally adjusted for trans fatty acid intake. Rhee, S. Lipopolysaccharide: basic biochemistry, intracellular signaling, and physiological impacts in the gut. Intest Res 12 , 90—95 Brun, P. Increased intestinal permeability in obese mice: new evidence in the pathogenesis of nonalcoholic steatohepatitis.

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Inulin controls inflammation and metabolic endotoxemia in women with type 2 diabetes mellitus: a randomized-controlled clinical trial. Int J Food Sci Nutr 65 , — Liu, Y. Last updated on June 21st, Salmonella-Shigella SS agar is used for selective isolation and differentiation of Salmonella and Shigella. It is used for the isolation, cultivation and differentiation of gram-negative enteric microorganisms from both […]. Last updated on June 21st, Salmonella is a member of the family Enterobacteriaceae.

It is a Gram-negative bacilli, motile and non-lactose fermenter. The genus can be divided into two species S. Last updated on June 30th, Although most prokaryotes cannot survive in nature without their cell walls, some do so naturally.

These include the mycoplasmas, a group of pathogenic bacteria that causes several infectious diseases […]. News Ticker.



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