Woods J P, Heinecke E L, Goldman W E
Department of Medical Microbiology and Immunology, University of Wisconsin Medical School, Madison 53706, USA.
Infect Immun. 1998 Apr;66(4):1697-707. doi: 10.1128/IAI.66.4.1697-1707.1998.
We developed an efficient electrotransformation system for the pathogenic fungus Histoplasma capsulatum and used it to examine the effects of features of the transforming DNA on transformation efficiency and fate of the transforming DNA and to demonstrate fungal expression of two recombinant Escherichia coli genes, hph and lacZ. Linearized DNA and plasmids containing Histoplasma telomeric sequences showed the greatest transformation efficiencies, while the plasmid vector had no significant effect, nor did the derivation of the selectable URA5 marker (native Histoplasma gene or a heterologous Podospora anserina gene). Electrotransformation resulted in more frequent multimerization, other modification, or possibly chromosomal integration of transforming telomeric plasmids when saturating amounts of DNA were used, but this effect was not observed with smaller amounts of transforming DNA. We developed another selection system using a hygromycin B resistance marker from plasmid pAN7-1, consisting of the E. coli hph gene flanked by Aspergillus nidulans promoter and terminator sequences. Much of the heterologous fungal sequences could be removed without compromising function in H. capsulatum, allowing construction of a substantially smaller effective marker fragment. Transformation efficiency increased when nonselective conditions were maintained for a time after electrotransformation before selection with the protein synthesis inhibitor hygromycin B was imposed. Finally, we constructed a readily detectable and quantifiable reporter gene by fusing Histoplasma URA5 with E. coli lacZ, resulting in expression of functional beta-galactosidase in H. capsulatum. Demonstration of expression of bacterial genes as effective selectable markers and reporters, together with a highly efficient electrotransformation system, provide valuable approaches for molecular genetic analysis and manipulation of H. capsulatum, which have proven useful for examination of targeted gene disruption, regulated gene expression, and potential virulence determinants in this fungus.
我们为致病性真菌荚膜组织胞浆菌开发了一种高效的电转化系统,并利用该系统研究转化DNA的特征对转化效率和转化DNA命运的影响,以及证明两个重组大肠杆菌基因hph和lacZ在真菌中的表达。线性化DNA和含有荚膜组织胞浆菌端粒序列的质粒显示出最高的转化效率,而质粒载体没有显著影响,可选择的URA5标记(荚膜组织胞浆菌天然基因或异源的嗜热栖热放线菌基因)的来源也没有显著影响。当使用饱和量的DNA时,电转化导致转化的端粒质粒更频繁地多聚化、其他修饰或可能的染色体整合,但使用较少量的转化DNA时未观察到这种效应。我们利用质粒pAN7-1中的潮霉素B抗性标记开发了另一种选择系统,该标记由侧翼为构巢曲霉启动子和终止子序列的大肠杆菌hph基因组成。许多异源真菌序列可以去除而不影响其在荚膜组织胞浆菌中的功能,从而允许构建一个实质上更小的有效标记片段。在用电转化法转化后,在施加蛋白质合成抑制剂潮霉素B进行选择之前,维持一段时间的非选择性条件,转化效率会提高。最后,我们通过将荚膜组织胞浆菌URA5与大肠杆菌lacZ融合,构建了一个易于检测和定量的报告基因,从而在荚膜组织胞浆菌中表达功能性β-半乳糖苷酶。证明细菌基因作为有效的选择标记和报告基因的表达,以及高效的电转化系统,为荚膜组织胞浆菌的分子遗传分析和操作提供了有价值的方法,这些方法已被证明可用于研究该真菌中的靶向基因破坏、调控基因表达和潜在的毒力决定因素。