Feng B, Wang X, Hauser M, Kaufmann S, Jentsch S, Haase G, Becker J M, Szaniszlo P J
Section of Molecular Genetics and Microbiology, Institute for Cellular and Molecular Biology, The University of Texas at Austin, Austin, Texas 78712, USA.
Infect Immun. 2001 Mar;69(3):1781-94. doi: 10.1128/IAI.69.3.1781-1794.2001.
1,8-Dihydroxynaphthalene (1,8-DHN) is a fungal polyketide that contributes to virulence when polymerized to 1,8-DHN melanin in the cell walls of Wangiella dermatitidis, an agent of phaeohyphomycosis in humans. To begin a genetic analysis of the initial synthetic steps leading to 1,8-DHN melanin biosynthesis, a 772-bp PCR product was amplified from genomic DNA using primers based on conserved regions of fungal polyketide synthases (Pks) known to produce the first cyclized 1,8-DHN-melanin pathway intermediate, 1,3,6,8-tetrahydroxynaphthalene. The cloned PCR product was then used as a targeting sequence to disrupt the putative polyketide synthase gene, WdPKS1, in W. dermatitidis. The resulting wdpks1Delta disruptants showed no morphological defects other than an albino phenotype and grew at the same rate as their black wild-type parent. Using a marker rescue approach, the intact WdPKS1 gene was then successfully recovered from two plasmids. The WdPKS1 gene was also isolated independently by complementation of the mel3 mutation in an albino mutant of W. dermatitidis using a cosmid library. Sequence analysis substantiated that WdPKS1 encoded a putative polyketide synthase (WdPks1p) in a single open reading frame consisting of three exons separated by two short introns. This conclusion was supported by the identification of highly conserved Pks domains for a beta-ketoacyl synthase, an acetyl-malonyl transferase, two acyl carrier proteins, and a thioesterase in the deduced amino acid sequence. Studies using a neutrophil killing assay and a mouse acute-infection model confirmed that all wdpks1Delta strains were less resistant to killing and less virulent, respectively, than their wild-type parent. Reconstitution of 1,8-DHN melanin biosynthesis in a wdpks1Delta strain reestablished its resistance to killing by neutrophils and its ability to cause fatal mouse infections.
1,8 - 二羟基萘(1,8 - DHN)是一种真菌聚酮化合物,当它在人类皮肤着色芽生菌病病原体皮炎外瓶霉的细胞壁中聚合成1,8 - DHN黑色素时,会增强其毒力。为了对导致1,8 - DHN黑色素生物合成的初始合成步骤进行遗传分析,基于已知能产生第一个环化的1,8 - DHN - 黑色素途径中间体1,3,6,8 - 四羟基萘的真菌聚酮合酶(Pks)保守区域设计引物,从基因组DNA中扩增出一个772 bp的PCR产物。然后将克隆的PCR产物用作靶向序列,破坏皮炎外瓶霉中假定的聚酮合酶基因WdPKS1。所得的wdpks1Delta突变体除了白化病表型外没有其他形态缺陷,并且生长速度与黑色野生型亲本相同。使用标记拯救方法,然后成功地从两个质粒中回收了完整的WdPKS1基因。还通过使用粘粒文库互补皮炎外瓶霉白化突变体中的mel3突变,独立分离出了WdPKS1基因。序列分析证实,WdPKS1在一个由三个外显子和两个短内含子分隔的单一开放阅读框中编码一种假定的聚酮合酶(WdPks1p)。在推导的氨基酸序列中鉴定出β - 酮酰基合酶、乙酰 - 丙二酰转移酶、两个酰基载体蛋白和一个硫酯酶的高度保守的Pks结构域,支持了这一结论。使用中性粒细胞杀伤试验和小鼠急性感染模型的研究证实,所有wdpks1Delta菌株分别比其野生型亲本对杀伤的抵抗力更低且毒力更弱。在wdpks1Delta菌株中重建1,8 - DHN黑色素生物合成,恢复了其对中性粒细胞杀伤的抵抗力以及引起致命小鼠感染的能力。