In vivo growth of Pseudomonas aeruginosa strains PAO1 and PA14 and the hypervirulent strain LESB58 in a rat model of chronic lung infection

被引:71
作者
Kukavica-Ibrulj, Irena [1 ]
Bragonzi, Alessandra [2 ]
Paroni, Moira [2 ]
Winstanley, Craig [4 ]
Sanschagrin, Francois [1 ]
O'Toole, George A. [3 ]
Levesque, Roger C. [1 ]
机构
[1] Univ Laval, Fac Med, Ctr Rech Fonct, Quebec City, PQ G1K 7P4, Canada
[2] HS Raffaele Scientif Inst, Inst Expt Treatment Cyct Fibrosis, Milan, Italy
[3] Dartmouth Coll, Hitchcock Med Ctr, Dartmouth Med Sch, Dept Microbiol & Immunol, Hanover, NH 03755 USA
[4] Univ Liverpool, Div Med Microbiol & Genitourinary Med, Liverpool L69 3GA, Merseyside, England
关键词
D O I
10.1128/JB.01572-07
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Pseudomonas aeruginosa chronic lung infections are the major cause of morbidity and mortality in cystic fibrosis (CF) patients. The P. aeruginosa strains PAO1 and PA14 were compared with the Liverpool epidemic strain LESB58 to assess in vivo growth, infection kinetics, and bacterial persistence and localization within tissues in a rat model of chronic lung infection. The three P. aeruginosa strains demonstrated similar growth curves in vivo but differences in tissue distribution. The LESB58 strain persisted in the bronchial lumen, while the PAO1 and PA14 strains were found localized in the alveolar regions and grew as macrocolonies after day 7 postinfection. Bacterial strains were compared for swimming and twitching motility and for the production of biofilm. The P. aeruginosa LESB58 strain produced more biofilm than PAO1 and PA14. Competitive index (CI) analysis of PAO1, PA14, and LESB58 in vivo indicated CI values of 0.002, 0.0002, and 0.14 between PAO1-PA14, PAO1-LESB58, and LESB58-PA14, respectively. CI analysis comparing the in vivo growth of the PAO1 Delta PA5441 mutant and four PA14 surface attachment-defective (sad) mutants gave C1 values 10 to 1,000 times lower in competitions with their respective wild-type strains PAO1 and PA14. P. aeruginosa strains studied in the rat model of chronic lung infection demonstrated similar in vivo growth but differences in virulence as shown with a competitive in vivo assay. These differences were further confirmed with biofilm and motility in vitro assays, where strain LESB58 produced more biofilm but had less capacity for motility than PAO1 and PA14.
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页码:2804 / 2813
页数:10
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