Kukavica-Ibrulj Irena, Bragonzi Alessandra, Paroni Moira, Winstanley Craig, Sanschagrin François, O'Toole George A, Levesque Roger C
Centre de Recherche sur la Fonction, Structure et Ingénierie des Protéines, Pavillon Charles-Eugène Marchand, Biologie Médicale, Faculté de Médecine, Université Laval, Laval, Québec G1K 7P4, Canada.
J Bacteriol. 2008 Apr;190(8):2804-13. doi: 10.1128/JB.01572-07. Epub 2007 Dec 14.
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 DeltaPA5441 mutant and four PA14 surface attachment-defective (sad) mutants gave CI 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.
铜绿假单胞菌慢性肺部感染是囊性纤维化(CF)患者发病和死亡的主要原因。将铜绿假单胞菌菌株PAO1和PA14与利物浦流行菌株LESB58进行比较,以评估慢性肺部感染大鼠模型中的体内生长、感染动力学以及细菌在组织内的持久性和定位。这三种铜绿假单胞菌菌株在体内显示出相似的生长曲线,但在组织分布上存在差异。LESB58菌株在支气管腔内持续存在,而PAO1和PA14菌株在感染后第7天被发现定位于肺泡区域并形成大菌落生长。比较了细菌菌株的游动和颤动运动能力以及生物膜的产生情况。铜绿假单胞菌LESB58菌株产生的生物膜比PAO1和PA14更多。PAO1、PA14和LESB58在体内的竞争指数(CI)分析表明,PAO1与PA14、PAO1与LESB58、LESB58与PA14之间的CI值分别为0.002、0.0002和0.14。比较PAO1 ΔPA5441突变体和四个PA14表面附着缺陷(sad)突变体的体内生长的CI分析表明,在与各自的野生型菌株PAO1和PA14的竞争中,CI值低10至1000倍。在慢性肺部感染大鼠模型中研究的铜绿假单胞菌菌株在体内生长相似,但如体内竞争试验所示,毒力存在差异。这些差异通过体外生物膜和运动试验进一步得到证实,其中LESB58菌株产生更多生物膜,但与PAO1和PA14相比,运动能力较弱。