Sequential genotyping of Pseudomonas aeruginosa from upper and lower airways of cystic fibrosis patients

被引:49
作者
Jung, A
Kleinau, I
Schönian, G
Bauernfeind, A
Chen, C
Griese, M
Döring, G
Göbel, U
Wahn, U
Paul, K
机构
[1] Humboldt Univ, Childrens Univ Hosp, Med Fac Charite, Berlin, Germany
[2] Humboldt Univ, Inst Microbiol & Hyg, Med Fac Charite, Berlin, Germany
[3] Univ Munich, Max Pettenkofer Inst Microbiol & Hyg, Munich, Germany
[4] Univ Munich, Childrens Univ Hosp, Munich, Germany
[5] Univ Tubingen, Inst Hyg, Tubingen, Germany
关键词
bronchoalveolar lavage; cystic fibrosis; Pseudomonas aeruginosa; pulsed-field gel electrophoresis; restriction fragment length polymorphism;
D O I
10.1183/09031936.02.00268002
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
A controversy exists concerning the adequate specimen to characterise colonisation of cystic fibrosis (CF) airways by Pseudomonas aeruginosa. Oropharyngeal, sputum and bronchoalveolar lavage samples were evaluated from 38 stable CF patients for the detection of P. aeruginosa, genetically different isolates within the same host and longitudinal variations in the genotype during repeated examinations. Bacterial isolates were typed by pulsed-field gel electrophoresis of deoxyribonucleic acid macrorestriction fragments. Sensitivity, negative and positive predictive values and specificity to detect P. aeruginosa were 35.7, 73.5, 83.3 and 96.2% for oropharyngeal cultures in nonexpectorating patients and 91.7, 94.1, 100 and 100% for sputum cultures from expectorating patients, respectively. Genotypes of Pseudomonas isolates recovered from oropharyngeal swabs and sputum differed to the strains recovered by bronchoscopy in 55% and 40%, respectively. In 62% longitudinal variations in the genotype occurred. One-half of these alterations were detectable by bronchoscopy only. In conclusion, sputum samples were of equal value as specimens from bronchoalveolar lavage to detect Pseudomonas aeruginosa colonisation. Cultures from the oropharynx are not suitable for characterising bacterial conditions in the cystic fibrosis lung. Different genotypes within the same host and longitudinal genetic alterations are common and may be detectable in the bronchoalveolar lavage fluid exclusively.
引用
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页码:1457 / 1463
页数:7
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