Pediatric Cystic Fibrosis Sputum Can Be Chemically Dynamic, Anoxic, and Extremely Reduced Due to Hydrogen Sulfide Formation
暂无分享,去创建一个
[1] L. Lynd,et al. Coculture of Staphylococcus aureus with Pseudomonas aeruginosa Drives S. aureus towards Fermentative Metabolism and Reduced Viability in a Cystic Fibrosis Model , 2015, Journal of bacteriology.
[2] M. Whiteman,et al. Hydrogen sulfide and nitric oxide interactions in inflammation. , 2014, Nitric oxide : biology and chemistry.
[3] Dean Chapman,et al. Pseudomonas aeruginosa triggers CFTR-mediated airway surface liquid secretion in swine trachea , 2014, Proceedings of the National Academy of Sciences.
[4] S. Amalfitano,et al. Effects of water stratification and mixing on microbial community structure in a subtropical deep reservoir , 2014, Scientific Reports.
[5] D. Hess,et al. Aminoglycoside inhibition of Staphylococcus aureus biofilm formation is nutrient dependent. , 2014, Journal of medical microbiology.
[6] A. Stock,et al. Living at the Limits: Evidence for Microbial Eukaryotes Thriving under Pressure in Deep Anoxic, Hypersaline Habitats , 2014 .
[7] M. Sogin,et al. The microbiome in pediatric cystic fibrosis patients: the role of shared environment suggests a window of intervention , 2014, Microbiome.
[8] D. Newman,et al. Phenazine redox cycling enhances anaerobic survival in Pseudomonas aeruginosa by facilitating generation of ATP and a proton‐motive force , 2014, Molecular microbiology.
[9] K. Turner,et al. Metatranscriptomics of the Human Oral Microbiome during Health and Disease , 2014, mBio.
[10] Forest Rohwer,et al. Biogeochemical Forces Shape the Composition and Physiology of Polymicrobial Communities in the Cystic Fibrosis Lung , 2014, mBio.
[11] A. Kharazmi,et al. Nitrous Oxide Production in Sputum from Cystic Fibrosis Patients with Chronic Pseudomonas aeruginosa Lung Infection , 2014, PloS one.
[12] K. Chung. Hydrogen sulfide as a potential biomarker of asthma , 2014, Expert review of respiratory medicine.
[13] M. Follows,et al. Morphological optimization for access to dual oxidants in biofilms , 2013, Proceedings of the National Academy of Sciences.
[14] Deborah A Hogan,et al. Unique microbial communities persist in individual cystic fibrosis patients throughout a clinical exacerbation , 2013, Microbiome.
[15] Robert E W Hancock,et al. Bacterial biofilm development as a multicellular adaptation: antibiotic resistance and new therapeutic strategies. , 2013, Current opinion in microbiology.
[16] D. Newman,et al. Ferrous Iron Is a Significant Component of Bioavailable Iron in Cystic Fibrosis Airways , 2013, mBio.
[17] B. Baker,et al. The microbiology of deep-sea hydrothermal vent plumes: ecological and biogeographic linkages to seafloor and water column habitats , 2013, Front. Microbiol..
[18] D. Willner,et al. Metagenomics and metatranscriptomics: windows on CF-associated viral and microbial communities. , 2013, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[19] B. Ryall,et al. Metabolic adaptations of Pseudomonas aeruginosa during cystic fibrosis chronic lung infections. , 2013, Environmental microbiology.
[20] A. Teske. Tracking microbial habitats in subseafloor sediments , 2012, Proceedings of the National Academy of Sciences.
[21] Shengchang Su,et al. Anaerobic Pseudomonas aeruginosa and other obligately anaerobic bacterial biofilms growing in the thick airway mucus of chronically infected cystic fibrosis patients: an emerging paradigm or “Old Hat”? , 2012, Expert opinion on therapeutic targets.
[22] D. Newman,et al. Phenazine content in the cystic fibrosis respiratory tract negatively correlates with lung function and microbial complexity. , 2012, American journal of respiratory cell and molecular biology.
[23] Ming Yan,et al. Correlation between serum H2S and pulmonary function in children with bronchial asthma. , 2012, Molecular medicine reports.
[24] Curtis Huttenhower,et al. Microbial Co-occurrence Relationships in the Human Microbiome , 2012, PLoS Comput. Biol..
[25] Karline Soetaert,et al. Erratum to "Reactive transport in aquatic ecosystems: Rapid model prototyping in the open source software R" [Environ. Modell. Softw. 32(2012) 49-60] , 2012, Environ. Model. Softw..
[26] Karline Soetaert,et al. Reactive transport in aquatic ecosystems: Rapid model prototyping in the open source software R , 2012, Environ. Model. Softw..
[27] E. Nudler,et al. H2S: A Universal Defense Against Antibiotics in Bacteria , 2011, Science.
[28] L. Hoffman,et al. Does bacterial density in cystic fibrosis sputum increase prior to pulmonary exacerbation? , 2011, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[29] C. von Buchwald,et al. Decreased mucosal oxygen tension in the maxillary sinuses in patients with cystic fibrosis. , 2011, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[30] W. Bowen,et al. Elevated Incidence of Dental Caries in a Mouse Model of Cystic Fibrosis , 2011, PloS one.
[31] D. Canfield,et al. Aerobic growth at nanomolar oxygen concentrations. , 2010 .
[32] A. Bakhrouf,et al. A microtiter plate assay for Staphylococcus aureus biofilm quantification at various pH levels and hydrogen peroxide supplementation. , 2010, The new microbiologica.
[33] S. Snyder,et al. Hydrogen sulfide as a gasotransmitter , 2010, Journal of neurochemistry.
[34] C. Barbosa,et al. The timing of diammonium phosphate supplementation of wine must affects subsequent H2S release during fermentation , 2010, Journal of applied microbiology.
[35] A. Kharazmi,et al. Polymorphonuclear leucocytes consume oxygen in sputum from chronic Pseudomonas aeruginosa pneumonia in cystic fibrosis , 2009, Thorax.
[36] A. Dozor,et al. Exhaled breath condensate pH and ammonia in cystic fibrosis and response to treatment of acute pulmonary exacerbations , 2009, Pediatric pulmonology.
[37] O. Ulloa,et al. Determination of ultra‐low oxygen concentrations in oxygen minimum zones by the STOX sensor , 2009 .
[38] Yen Cu,et al. Mathematical modeling of molecular diffusion through mucus. , 2009, Advanced drug delivery reviews.
[39] S. Ragsdale,et al. Acetogenesis and the Wood-Ljungdahl pathway of CO(2) fixation. , 2008, Biochimica et biophysica acta.
[40] P. Španěl,et al. A study of sulfur-containing compounds in mouth- and nose-exhaled breath and in the oral cavity using selected ion flow tube mass spectrometry , 2008, Journal of breath research.
[41] Karline Soetaert,et al. A Practical Guide to Ecological Modelling: Using R as a Simulation Platform , 2008 .
[42] B. Costello,et al. A sensor system for monitoring the simple gases hydrogen, carbon monoxide, hydrogen sulfide, ammonia and ethanol in exhaled breath , 2008, Journal of breath research.
[43] D. Newman,et al. Redox reactions of phenazine antibiotics with ferric (hydr)oxides and molecular oxygen. , 2008, Environmental science & technology.
[44] M. Lieberman,et al. Proteomic, Microarray, and Signature-Tagged Mutagenesis Analyses of Anaerobic Pseudomonas aeruginosa at pH 6.5, Likely Representing Chronic, Late-Stage Cystic Fibrosis Airway Conditions , 2008, Journal of bacteriology.
[45] M. Whiteley,et al. Nutritional Cues Control Pseudomonas aeruginosa Multicellular Behavior in Cystic Fibrosis Sputum , 2007, Journal of bacteriology.
[46] C. Harwood,et al. Responses of Pseudomonas aeruginosa to low oxygen indicate that growth in the cystic fibrosis lung is by aerobic respiration , 2007, Molecular microbiology.
[47] C. Haidaris,et al. Nitrate Sensing and Metabolism Modulate Motility, Biofilm Formation, and Virulence in Pseudomonas aeruginosa , 2007, Infection and Immunity.
[48] R. Boucher. Airway surface dehydration in cystic fibrosis: pathogenesis and therapy. , 2007, Annual review of medicine.
[49] J. Wallace,et al. Hydrogen sulfide is an endogenous modulator of leukocyte‐mediated inflammation , 2006, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[50] David A. D'Argenio,et al. Genetic adaptation by Pseudomonas aeruginosa to the airways of cystic fibrosis patients. , 2006, Proceedings of the National Academy of Sciences of the United States of America.
[51] D. Blake,et al. Breath sulfides and pulmonary function in cystic fibrosis. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[52] Yahong Chen,et al. Endogenous hydrogen sulfide in patients with COPD. , 2005, Chest.
[53] C. Haidaris,et al. Effect of Anaerobiosis and Nitrate on Gene Expression in Pseudomonas aeruginosa , 2005, Infection and Immunity.
[54] R. Novick,et al. Effect of Mild Acid on Gene Expression in Staphylococcus aureus , 2004, Journal of bacteriology.
[55] P. Davis,et al. State of the Art: Why do the lungs of patients with cystic fibrosis become infected and why can't they clear the infection? , 2003, Respiratory research.
[56] Philip S. Stewart,et al. Diffusion in Biofilms , 2003, Journal of bacteriology.
[57] Z. Lewandowski,et al. The double substrate growth kinetics of Pseudomonas aeruginosa , 2003 .
[58] J. Innes,et al. Airways in cystic fibrosis are acidified: detection by exhaled breath condensate , 2002, Thorax.
[59] George M. Hilliard,et al. Pseudomonas aeruginosa anaerobic respiration in biofilms: relationships to cystic fibrosis pathogenesis. , 2002, Developmental cell.
[60] Gerald B. Pier,et al. Lung Infections Associated with Cystic Fibrosis , 2002, Clinical Microbiology Reviews.
[61] M. Knowles,et al. Mucus clearance as a primary innate defense mechanism for mammalian airways. , 2002, The Journal of clinical investigation.
[62] Richard C Boucher,et al. Effects of reduced mucus oxygen concentration in airway Pseudomonas infections of cystic fibrosis patients. , 2002, The Journal of clinical investigation.
[63] N. Revsbech,et al. An oxygen insensitive microsensor for nitrous oxide , 2001 .
[64] N. Høiby,et al. Diagnosis and Treatment of Cystic Fibrosis , 2000, Respiration.
[65] Tian C. Zhang,et al. Fabrication of Redox Potential Microelectrodes for Studies in Vegetated Soils or Biofilm Systems , 1998 .
[66] P. Stewart,et al. Spatial Physiological Heterogeneity inPseudomonas aeruginosa Biofilm Is Determined by Oxygen Availability , 1998, Applied and Environmental Microbiology.
[67] M. Kühl,et al. A H2S microsensor for profiling biofilms and sediments: application in an acidic lake sediment , 1998 .
[68] D. Sims,et al. Heterogeneity of the composition and thickness of tracheal mucus in rats. , 1997, The American journal of physiology.
[69] Michael Kühl,et al. An amperometric microsensor for the determination of H2S in aquatic environments , 1996 .
[70] D. Hassett. Anaerobic production of alginate by Pseudomonas aeruginosa: alginate restricts diffusion of oxygen , 1996, Journal of bacteriology.
[71] R. T. Rosen,et al. Breath Analysis of Garlic-Borne Phytochemicals in Human Subjects: Combined Adsorbent Trapping and Short-Path Thermal Desorption Gas Chromatography—Mass Spectrometry , 1993 .
[72] N. Høiby,et al. Pathogenesis of cystic fibrosis , 1993, The Lancet.
[73] Janet G. Hering,et al. Principles and Applications of Aquatic Chemistry , 1993 .
[74] Louis I. Gordon,et al. Oxygen solubility in seawater : better fitting equations , 1992 .
[75] G. Macfarlane,et al. Growth and activities of sulphate-reducing bacteria in gut contents of healthy subjects and patients with ulcerative colitis , 1991 .
[76] N. Revsbech,et al. An oxygen microsensor with a guard cathode , 1989 .
[77] P. Visscher,et al. Production and Fate of Methylated Sulfur Compounds from Methionine and Dimethylsulfoniopropionate in Anoxic Salt Marsh Sediments , 1987, Applied and environmental microbiology.
[78] T. Gilat,et al. Methane Production in Patients with Cystic Fibrosis , 1987, Journal of pediatric gastroenterology and nutrition.
[79] A. Piérard,et al. Pseudomonas aeruginosa mutants affected in anaerobic growth on arginine: evidence for a four-gene cluster encoding the arginine deiminase pathway , 1984, Journal of bacteriology.
[80] B. Babior,et al. The particulate superoxide-forming system from human neutrophils. Properties of the system and further evidence supporting its participation in the respiratory burst. , 1976, The Journal of clinical investigation.
[81] D. Harrison. Physiological effects of dissolved oxygen tension and redox potential on growing populations of micro-organisms , 1972 .
[82] M. Kühl,et al. Denitrification by cystic fibrosis pathogens - Stenotrophomonas maltophilia is dormant in sputum. , 2015, International journal of medical microbiology : IJMM.
[83] C. H. K. Wu. The role of hydrogen sulphide in lung diseases , 2013 .
[84] S. Lory,et al. Phylogenetic and metabolic diversity of bacteria associated with cystic fibrosis , 2011, The ISME Journal.
[85] R. Tarran,et al. Methods for ASL measurements and mucus transport rates in cell cultures. , 2011, Methods in molecular biology.
[86] C. Fuqua,et al. Bacterial competition: surviving and thriving in the microbial jungle , 2010, Nature Reviews Microbiology.
[87] P. Herman,et al. A Practical Guide to Ecological Modelling , 2009 .
[88] R. B. Hespell,et al. Amino acid and glucose fermentation by Treponema denticola , 2004, Archiv für Mikrobiologie.
[89] F. Saraví,et al. Oxygen diffusive barriers of rat distal colon: role of subepithelial tissue, mucosa, and mucus gel layer. , 2000, Digestive diseases and sciences.
[90] Chi-Tang Ho,et al. Food phytochemicals for cancer prevention , 1994 .
[91] L. Tsui,et al. Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA. , 1989, Science.
[92] J. Noebels. Ion-Sensitive Intracellular Microelectrodes. How to Make and Use Them , 1979, The Yale Journal of Biology and Medicine.
[93] Y. Ishida,et al. Production of volatile sulfur compounds by microorganisms. , 1972, Annual review of microbiology.
[94] J. J. Morgan,et al. Aquatic Chemistry: Chemical Equilibria and Rates in Natural Waters , 1970 .
[95] M. Tian,et al. Correlation between serum H 2 S and pulmonary function in children with bronchial asthma , 2022 .