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通过签名标签插入诱变鉴定ENA1作为人类致病真菌新型隐球菌的毒力基因。

Identification of ENA1 as a virulence gene of the human pathogenic fungus Cryptococcus neoformans through signature-tagged insertional mutagenesis.

作者信息

Idnurm Alexander, Walton Felicia J, Floyd Anna, Reedy Jennifer L, Heitman Joseph

机构信息

Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, North Carolina 27710, USA.

出版信息

Eukaryot Cell. 2009 Mar;8(3):315-26. doi: 10.1128/EC.00375-08. Epub 2009 Jan 16.

Abstract

A library of more than 4,500 signature-tagged insertion mutants of the human pathogenic fungus Cryptococcus neoformans was generated, and a subset was screened in a murine inhalation model to identify genes required for virulence. New genes that regulate aspects of C. neoformans virulence were also identified by screening the entire library for in vitro phenotypes related to the ability to cause disease, including melanin production, growth at high temperature, and growth under conditions of nutrient limitation. A screen of 10% of the strain collection in mice identified an avirulent mutant strain with an insertion in the ENA1 gene, which is predicted to encode a fungus-specific sodium or potassium P-type ATPase. The results of the deletion of the gene and complementation experiments confirmed its key role in mammalian virulence. ena1 mutant strains exhibited no change in sensitivity to high salt concentrations but were sensitive to alkaline pH conditions, providing evidence that the fungus may have to survive at elevated pH during infection of the mammalian host. The mutation of the well-characterized virulence factor calcineurin (CNA1) also rendered C. neoformans strains sensitive to elevated pH. ENA1 transcripts in wild-type and cna1 mutant strains were upregulated in response to high pH, and cna1 ena1 double mutant strains exhibited increased sensitivity to elevated pH, indicating that at least two pathways in the fungus mediate survival under alkaline conditions. Signature-tagged mutagenesis is an effective strategy for the discovery of new virulence genes in fungal pathogens of animals.

摘要

构建了一个包含超过4500个人类致病真菌新型隐球菌签名标签插入突变体的文库,并在小鼠吸入模型中筛选了一个子集,以鉴定毒力所需的基因。通过筛选整个文库中与致病能力相关的体外表型,包括黑色素产生、高温生长和营养限制条件下的生长,还鉴定了调节新型隐球菌毒力方面的新基因。在小鼠中对10%的菌株进行筛选,鉴定出一个在ENA1基因中有插入的无毒突变菌株,该基因预计编码一种真菌特异性钠或钾P型ATP酶。基因缺失和互补实验的结果证实了其在哺乳动物毒力中的关键作用。ena1突变菌株对高盐浓度的敏感性没有变化,但对碱性pH条件敏感,这表明真菌在感染哺乳动物宿主期间可能必须在升高的pH值下存活。特征明确的毒力因子钙调神经磷酸酶(CNA1)的突变也使新型隐球菌菌株对升高的pH敏感。野生型和cna1突变菌株中的ENA1转录本在高pH响应中上调,cna1 ena1双突变菌株对升高的pH表现出更高的敏感性,表明真菌中至少有两条途径介导碱性条件下的存活。签名标签诱变是发现动物真菌病原体中新毒力基因的有效策略。

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