Monod M, Paris S, Sarfati J, Jaton-Ogay K, Ave P, Latgé J P
Service de Dermatologie, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.
FEMS Microbiol Lett. 1993 Jan 1;106(1):39-46. doi: 10.1111/j.1574-6968.1993.tb05932.x.
The gene encoding the secreted alkaline protease, a suspected virulence factor of Aspergillus fumigatus, was inactivated by gene disruption. The disruption was performed by transformation of a pathogenic strain of the fungus with a linear DNA fragment carrying the gene from which the central part was replaced by the selectable Escherichia coli hygromycin B dominant resistance marker. Two transformants were shown to produce no alkaline protease. Restriction fragment analysis of the DNA of these two transformants was consistent for chromosomal integration of the disrupted gene by homologous recombination. Both isogenic alkaline protease-producing and non-producing A. fumigatus strains invaded lung tissues, causing comparable mortality in immunosuppressed mice. A significant residual proteolytic activity observed in alkaline protease non-producing strain cultures could play a role in the invasion of the tissues by the fungus.
编码分泌性碱性蛋白酶(烟曲霉一种潜在的毒力因子)的基因通过基因敲除使其失活。基因敲除是通过用携带该基因的线性DNA片段转化该真菌的致病菌株来进行的,该片段的中央部分被可选择的大肠杆菌潮霉素B显性抗性标记所取代。两个转化体均显示不产生碱性蛋白酶。对这两个转化体的DNA进行限制性片段分析,结果与通过同源重组使被破坏的基因整合到染色体上相一致。同源的产碱性蛋白酶和不产碱性蛋白酶的烟曲霉菌株均侵袭肺组织,在免疫抑制小鼠中导致相当的死亡率。在不产碱性蛋白酶的菌株培养物中观察到的显著残余蛋白水解活性可能在真菌对组织的侵袭中起作用。