Nelson R T, Hua J, Pryor B, Lodge J K
Edward A. Doisy Department of Biochemistry and Molecular Biology, Saint Louis University School of Medicine, St. Louis, Missouri 63104, USA.
Genetics. 2001 Mar;157(3):935-47. doi: 10.1093/genetics/157.3.935.
Cryptococcus neoformans var. neoformans is an important opportunistic fungal pathogen of patients whose immune system has been compromised due to viral infection, antineoplastic chemotherapy, or tissue transplantation. As many as 13% of all AIDS patients suffer a life-threatening cryptococcal infection at some time during the course of their HIV disease. To begin to understand the molecular basis for virulence in Cryptococcus neoformans var. neoformans serotype A, we have employed signature-tagged mutagenesis (STM) to identify mutants with altered virulence in a mouse model. The critical parameters of signature-tagged mutagenesis in C. neoformans are explored. Data are presented showing that at least 100 different strains can be mixed together in a single animal with each participating in the infection and that there is no apparent interaction between a virulent strain and an avirulent strain in our animal model. Using signature-tagged mutagenesis, we identified 39 mutants with significantly altered growth in a competitive assay. Molecular analyses of these mutants indicated that 19 (49%) contained an insertion in the actin promoter by homologous recombination from a single crossover event, creating a duplication of the actin promoter and the integration of single or multiple copies of the vector. Analysis of the chromosomal insertion sites of those mutants that did not have an integration event in the actin promoter revealed an approximately random distribution among the chromosomes. Individual challenge of the putative mutants in a mouse model revealed five hypovirulent mutants and one hypervirulent mutant.
新型隐球菌新生变种是一种重要的机会性真菌病原体,可感染因病毒感染、抗肿瘤化疗或组织移植而导致免疫系统受损的患者。在所有艾滋病患者中,多达13%在其感染人类免疫缺陷病毒(HIV)的病程中的某个时候会遭受危及生命的隐球菌感染。为了开始了解新型隐球菌新生变种血清型A毒力的分子基础,我们采用了签名标签诱变技术(STM)来在小鼠模型中鉴定毒力改变的突变体。我们探索了新型隐球菌中签名标签诱变的关键参数。所呈现的数据表明,至少100种不同的菌株可以在一只动物体内混合在一起,每种菌株都参与感染,并且在我们的动物模型中,有毒力的菌株和无毒力的菌株之间没有明显的相互作用。利用签名标签诱变技术,我们在竞争试验中鉴定出39个生长有显著改变的突变体。对这些突变体的分子分析表明,19个(49%)通过单次交叉事件的同源重组在肌动蛋白启动子中含有一个插入,产生了肌动蛋白启动子的重复以及载体单拷贝或多拷贝的整合。对那些在肌动蛋白启动子中没有整合事件的突变体的染色体插入位点分析显示,它们在染色体之间大致呈随机分布。在小鼠模型中对假定的突变体进行单独攻击,发现了5个弱毒力突变体和1个强毒力突变体。