Polak A
F. Hoffmann-La Roche Ltd, Pharma Division, Basel, Switzerland.
Mycoses. 1992 Jan-Feb;35(1-2):9-16. doi: 10.1111/j.1439-0507.1992.tb00813.x.
Mutant strains of the fungal pathogen Candida albicans blocked in pyrimidine transport and salvage metabolism were tested for virulence in various animal models. The growth rate, germination and proteolytic enzyme production did not correlate with the virulence of the strains. However, a defect in the uridine transport system significantly decreased virulence in murine candidosis, although it had no effect in vaginal candidosis or in a Candida cyst model. It remains unclear whether this is due to the differing host defence mechanisms involved in systemic and superficial mycoses, or to the different requirements of the fungal systems for adherence and tissue invasion in the two types of infection.
对嘧啶转运和补救代谢受阻的真菌病原体白色念珠菌突变株在各种动物模型中进行了毒力测试。这些菌株的生长速率、发芽和蛋白酶产生与毒力无关。然而,尿苷转运系统的缺陷显著降低了小鼠念珠菌病的毒力,尽管它对阴道念珠菌病或念珠菌囊肿模型没有影响。目前尚不清楚这是由于全身和浅表真菌病中涉及的宿主防御机制不同,还是由于两种感染类型中真菌系统对黏附和组织侵袭的不同需求。