Molecular epidemiology of Pseudomonas aeruginosa

被引:44
作者
Speert, DP [1 ]
机构
[1] Childrens Variety Res Ctr, Vancouver, BC V5Z 4H4, Canada
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2002年 / 7卷
关键词
Pseudomonas aeruginosa; epidemiology; cystic fibrosis; neutropenia; burns; molecular epidemiology; pulsed field gel electrophoresis; random amplified polymorphic DNA; review;
D O I
10.2741/speert
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pseudomonas aeruginosa is a serious opportunistic pathogen in certain compromised hosts, such as those with cystic fibrosis, thermal burns and cancer. It also causes less severe noninvasive disease, such as otitis externa and hot tub folliculitis, in normal hosts. P. aeruginosa is phenotypically very unstable, particularly in patients with chronic infection. Phenotypic typing techniques are useful for understanding the epidemiology of acute infections, but they are limited by their discriminatory power and by their inability to group isolates that are phenotypically unrelated but genetically homologous. Molecular typing techniques, developed over the past decade, are highly discriminatory and are useful for typing strains from patients with chronic infection where the bacterial phenotype is unstable; this is particularly true in cystic fibrosis, where patients often are infected with the same strain for several decades, but the bacteria undergo phenotypic alteration. Molecular typing techniques, which have proven useful in typing P. aeruginosa for epidemiological purposes, include pulsed field gel electrophoresis, restriction fragment length polymorphic DNA analysis, random amplified polymorphic DNA analysis, repetitive extrapalindromic PCR analysis, and multilocus sequence typing. These methods are generally only available in specialized laboratories, but they should be used when data from phenotypic typing analysis are ambiguous or when phenotypic methods are unreliable, such as in cystic fibrosis.
引用
收藏
页码:E354 / E361
页数:8
相关论文
共 53 条
[1]  
Bauer T T, 2000, Semin Respir Infect, V15, P272
[2]  
Bergmans DCJJ, 1998, INFECT CONT HOSP EP, V19, P853
[3]   Cross-colonisation with Pseudomonas aeruginosa of patients in an intensive care unit [J].
Bergmans, DCJJ ;
Bonten, MJM ;
van Tiel, FH ;
Gaillard, CA ;
van der Geest, S ;
Wilting, RM ;
de Leeuw, PW ;
Stobberingh, EE .
THORAX, 1998, 53 (12) :1053-1058
[4]   Prospective study of nosocomial colonization and infection due to Pseudomonas aeruginosa in mechanically ventilated patients [J].
Berthelot, P ;
Grattard, E ;
Mahul, P ;
Pain, P ;
Jospé, R ;
Venet, C ;
Carricajo, A ;
Aubert, G ;
Ros, A ;
Dumont, A ;
Lucht, F ;
Zéni, F ;
Auboyer, C ;
Bertrand, JC ;
Pozzetto, B .
INTENSIVE CARE MEDICINE, 2001, 27 (03) :503-+
[5]   Pseudomonas aeruginosa infections in cancer patients:: have they gone away? [J].
Bodey, GP .
CURRENT OPINION IN INFECTIOUS DISEASES, 2001, 14 (04) :403-407
[6]   Characteristics of polyclonal endemicity of Pseudomonas aeruginosa colonization in intensive care units -: Implications for infection control [J].
Bonten, MJM ;
Bergmans, DCJJ ;
Speijer, H ;
Stobberingh, EE .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1999, 160 (04) :1212-1219
[7]  
Botzenhart K., 1993, Pseudomonas aeruginosa as an Opportunistic Pathogen, P1, DOI 10.1007/978-1-4615-3036-7_1
[8]  
Chastre J, 2000, Semin Respir Infect, V15, P287
[9]   Spread of beta-lactam-resistant Pseudomonas aeruginosa in a cystic fibrosis clinic [J].
Cheng, K ;
Smyth, RL ;
Govan, JRW ;
Doherty, C ;
Winstanley, C ;
Denning, N ;
Heaf, DP ;
vanSaene, H ;
Hart, CA .
LANCET, 1996, 348 (9028) :639-642
[10]   Analysis of epidemic Pseudomonas aeruginosa isolates by isoelectric focusing of pyoverdine and RAPD-PCR: modern tools for an integrated anti-nosocomial infection strategy in burn wound centres [J].
DeVos, D ;
Lim, A ;
Pirnay, JP ;
Duinslaeger, L ;
Revets, H ;
Vanderkelen, A ;
Hamers, R ;
Cornelis, P .
BURNS, 1997, 23 (05) :379-386