de Repentigny Louis
Department of Microbiology and Immunology, Sainte-Justine Hospital and University of Montreal, 3175 Côte Ste-Catherine, Montreal, Quebec, Canada, H3T 1C5.
Curr Opin Microbiol. 2004 Aug;7(4):324-9. doi: 10.1016/j.mib.2004.06.001.
An increasingly diverse array of clinically relevant animal models of candidiasis have been established that mimic both the immune perturbations of the host and tissue-specific features of candidiasis in humans. Cause-and-effect analysis of Candida host-pathogen interactions using these animal models has made a quantum leap forward in the genomic era, with the concurrent construction of C. albicans mutants with targeted mutations of putative virulence factors, the application of microarrays and other emerging technologies to comprehensively assess C. albicans gene expression in vivo, and construction of transgenic and knockout mice to simulate specific host immunodeficiencies. The opportunity to combine these powerful tools will yield an unprecedented wealth of new information on the molecular and cellular pathogenesis of candidiasis.
已经建立了越来越多样化的念珠菌病临床相关动物模型,这些模型既模拟了宿主的免疫紊乱,也模拟了人类念珠菌病的组织特异性特征。在基因组时代,使用这些动物模型对念珠菌宿主 - 病原体相互作用进行因果分析取得了巨大飞跃,同时构建了具有假定毒力因子靶向突变的白色念珠菌突变体,应用微阵列和其他新兴技术全面评估白色念珠菌在体内的基因表达,并构建转基因和基因敲除小鼠以模拟特定的宿主免疫缺陷。结合这些强大工具的机会将产生关于念珠菌病分子和细胞发病机制的前所未有的丰富新信息。