2011
DOI: 10.3390/ijerph8020554
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Prevalence and Antimicrobial-Resistance of Pseudomonas aeruginosa in Swimming Pools and Hot Tubs

Abstract: Pseudomonas aeruginosa is an important opportunistic pathogen in recreational waters and the primary cause of hot tub folliculitis and otitis externa. The aim of this surveillance study was to determine the background prevalence and antimicrobial resistance profile of P. aeruginosa in swimming pools and hot tubs. A convenience sample of 108 samples was obtained from three hot tubs and eight indoor swimming pools. Water and swab samples were processed using membrane filtration, followed by confirmation with pol… Show more

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Cited by 89 publications
(64 citation statements)
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“…Pseudomonas aeruginosa has intrinsic resistance to many antimicrobial agents including most penicillins, narrow-spectrum cephalosporins, cefotaxime, and also other compounds such as tetracycline and chloramphenicol, which in part explains the isolate's resistance phenotype obtained (Zhao and Hu, 2010;Lutz and Lee, 2011). However, E67 was found to have intermediate resistance to aztreonam, imipenem and meropenem, antibiotics which are considered to be clinically relevant antipseudomonal drugs (Magiorakos et al, 2012).…”
Section: Strain Phenotypic Analysismentioning
confidence: 99%
“…Pseudomonas aeruginosa has intrinsic resistance to many antimicrobial agents including most penicillins, narrow-spectrum cephalosporins, cefotaxime, and also other compounds such as tetracycline and chloramphenicol, which in part explains the isolate's resistance phenotype obtained (Zhao and Hu, 2010;Lutz and Lee, 2011). However, E67 was found to have intermediate resistance to aztreonam, imipenem and meropenem, antibiotics which are considered to be clinically relevant antipseudomonal drugs (Magiorakos et al, 2012).…”
Section: Strain Phenotypic Analysismentioning
confidence: 99%
“…All PCR assay was carried out using a Peltier-based thermal cycler (BioSeparation System, Shanxi, China) at the succeeding thermal cycler conditions: 95 °C for 1 min; 40 rounds of thermal denaturation at 95 °C for 15 s; primer annealing at 58 °C for 20 s; concluding extension at 68 °C for 40 s and holding temperature of 4 °C . P. aeruginosa primers used were pa722F (5'-GGCGTGGGTGTGGAAGTC-3') and pa899R (5'-TGGTGGCGATCT TGAACT TCTT-3') amplicon size of 199 bp [18]. Amplicons were electrophoresed with 1% agarose gel (Hispanagar, Spain) encompassing ethidium bromide 0.5 mg/L (Merck, SA) at 100 V for 1 h in 0.5 × tris-acetate-ethylene diamine tetraacetic acid buffer (40 mmol/L tris-HCl, 20 mmol/L Na-acetate, 1 mmol/L ethylene diamine tetraacetic acid, pH 8.5) and imagined under a UV transilluminator (EBOX VX5, Vilber Lourmat, France).…”
Section: Pcr Amplification Assaymentioning
confidence: 99%
“…Infections caused by this bacterium are difficult to root up because it has innate antimicrobial resistance due to low outer membrane permeability and an extensive efflux pump system [7]. However, genes make the bacteria more resistant to antibiotics such as β-lactams, aminoglycosides and fluoroquinolones acquired newly by this bacterium [8].…”
Section: Introductionmentioning
confidence: 99%