Cross-infection with Pseudomonas aeruginosa is rare in non-cystic fibrosis bronchiectasis http://ow.ly/sjvKz
نویسندگان
چکیده
Anthony De Soyza, Audrey Perry, Amanda J. Hall, Syba S. Sunny, Kathy E. Walton, Nazim Mustafa, Jane Turton, Dervla T. Kenna and Craig Winstanley Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, Sir William Leech Centre for Respiratory Research and Freeman Hospital Adult Bronchiectasis Unit, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, Dept of Medical Microbiology, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, Institute of Infection and Global Health, University of Liverpool, Liverpool, and Antimicrobial Resistance and Healthcare Associated Infections Reference Unit, Public Health England, London, UK.
منابع مشابه
Adherence of Pseudomonas aeruginosa to cystic fibrosis buccal epithelial cells
Pseudomonas aeruginosa cystic fibrosis buccal adherence assay http://ow.ly/lPtB306VKIQ.
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In patients with cystic fibrosis (CF) and non-CF bronchiectasis, Pseudomonas aeruginosa is the most important respiratory pathogen. It is able to synthesise hydrogen cyanide, a potent inhibitor of cellular respiration. The present study investigated whether cyanide is present in the sputum of CF and non-CF bronchiectasis patients infected with P. aeruginosa, and whether the detection of cyanide...
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1) Newcastle University, Institute of Cellular Medicine and 2) Sir William Leech Centre for Respiratory Research and Freeman Hospital Adult Bronchiectasis Unit, Newcastle upon Tyne Hospitals Trust, 3) Department of Medical Microbiology, The Newcastle upon Tyne Hospitals NHS Foundation Trust, 4) Institute of Infection and Global Health, University of Liverpool 5) Antibiotic Resistance and Health...
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Abstract Background and Objective: Cystic fibrosis (CF) is an autosomal recessive genetic disease and Pseudomonas aeruginosa is one of the most common bacteria colonized in CF patients. Growing resistance of this bacterium to antibiotics now a day is a challenge of controlling infection in CF patient. In this study colonization of CF patients with Pseudomonas aeruginosa and antibiotic suscep...
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Sixty four Iranian patients with cystic fibrosis (CF) were studied for colonization with Pseudomonasaeruginosa. The patient’s age ranged between 2 months to 18 years old. Twenty one patients werecolonized, 15 with non-mucoid and 6 with mucoid strains of P. aeruginosa. The colonization rateincreased with age and the mucoid phenotype was only recovered from the older patients. A...
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تاریخ انتشار 2014