Miyata Sachiko, Casey Monika, Frank Dara W, Ausubel Frederick M, Drenkard Eliana
Department of Genetics, Harvard Medical School, Boston, Massachusetts 02114, USA.
Infect Immun. 2003 May;71(5):2404-13. doi: 10.1128/IAI.71.5.2404-2413.2003.
Nonvertebrate model hosts represent valuable tools for the study of host-pathogen interactions because they facilitate the identification of bacterial virulence factors and allow the discovery of novel components involved in host innate immune responses. In this report, we determined that the greater wax moth caterpillar Galleria mellonella is a convenient nonmammalian model host for study of the role of the type III secretion system (TTSS) in Pseudomonas aeruginosa pathogenesis. Based on the observation that a mutation in the TTSS pscD gene of P. aeruginosa strain PA14 resulted in a highly attenuated virulence phenotype in G. mellonella, we examined the roles of the four known effector proteins of P. aeruginosa (ExoS, ExoT, ExoU, and ExoY) in wax moth killing. We determined that in P. aeruginosa strain PA14, only ExoT and ExoU play a significant role in G. mellonella killing. Strain PA14 lacks the coding sequence for the ExoS effector protein and does not seem to express ExoY. Moreover, using Delta exoU Delta exoY, Delta exoT Delta exoY, and Delta exoT Delta exoU double mutants, we determined that individual translocation of either ExoT or ExoU is sufficient to obtain nearly wild-type levels of G. mellonella killing. On the other hand, data obtained with a Delta exoT Delta exoU Delta exoY triple mutant and a Delta pscD mutant suggested that additional, as-yet-unidentified P. aeruginosa components of type III secretion are involved in virulence in G. mellonella. A high level of correlation between the results obtained in the G. mellonella model and the results of cytopathology assays performed with a mammalian tissue culture system validated the use of G. mellonella for the study of the P. aeruginosa TTSS.
非脊椎动物模型宿主是研究宿主-病原体相互作用的宝贵工具,因为它们有助于鉴定细菌毒力因子,并能发现宿主固有免疫反应中涉及的新成分。在本报告中,我们确定大蜡螟幼虫是研究III型分泌系统(TTSS)在铜绿假单胞菌致病机制中作用的便捷非哺乳动物模型宿主。基于对铜绿假单胞菌PA14菌株TTSS pscD基因突变导致其在大蜡螟中致病力显著减弱的观察,我们研究了铜绿假单胞菌四种已知效应蛋白(ExoS、ExoT、ExoU和ExoY)在杀死蜡螟中的作用。我们确定,在铜绿假单胞菌PA14菌株中,只有ExoT和ExoU在杀死大蜡螟中起重要作用。PA14菌株缺乏ExoS效应蛋白的编码序列,似乎也不表达ExoY。此外,使用缺失exoU缺失exoY、缺失exoT缺失exoY和缺失exoT缺失exoU双突变体,我们确定ExoT或ExoU的单独转运足以获得接近野生型水平的杀死大蜡螟能力。另一方面,用缺失exoT缺失exoU缺失exoY三突变体和缺失pscD突变体获得的数据表明,III型分泌的其他尚未鉴定的铜绿假单胞菌成分参与了大蜡螟的致病过程。在大蜡螟模型中获得的结果与在哺乳动物组织培养系统中进行的细胞病理学分析结果之间的高度相关性,验证了使用大蜡螟研究铜绿假单胞菌TTSS的可行性。