Paul Sanjoy, Diekema Daniel, Moye-Rowley W Scott
Departments of Molecular Physiology and Biophysics.
Eukaryot Cell. 2013 Dec;12(12):1619-28. doi: 10.1128/EC.00171-13. Epub 2013 Oct 11.
In yeast cells such as those of Saccharomyces cerevisiae, expression of ATP-binding cassette (ABC) transporter proteins has been found to be increased and correlates with a concomitant elevation in azole drug resistance. In this study, we investigated the roles of two Aspergillus fumigatus proteins that share high sequence similarity with S. cerevisiae Pdr5, an ABC transporter protein that is commonly overproduced in azole-resistant isolates in this yeast. The two A. fumigatus genes encoding the ABC transporters sharing the highest sequence similarity to S. cerevisiae Pdr5 are called abcA and abcB here. We constructed deletion alleles of these two different ABC transporter-encoding genes in three different strains of A. fumigatus. Loss of abcB invariably elicited increased azole susceptibility, while abcA disruption alleles had variable phenotypes. Specific antibodies were raised to both AbcA and AbcB proteins. These antisera allowed detection of AbcB in wild-type cells, while AbcA could be visualized only when overproduced from the hspA promoter in A. fumigatus. Overproduction of AbcA also yielded increased azole resistance. Green fluorescent protein fusions were used to provide evidence that both AbcA and AbcB are localized to the plasma membrane in A. fumigatus. Promoter fusions to firefly luciferase suggested that expression of both ABC transporter-encoding genes is inducible by azole challenge. Virulence assays implicated AbcB as a possible factor required for normal pathogenesis. This work provides important new insights into the physiological roles of ABC transporters in this major fungal pathogen.
在诸如酿酒酵母的酵母细胞中,已发现ATP结合盒(ABC)转运蛋白的表达增加,并且与唑类药物抗性的同时升高相关。在本研究中,我们调查了两种烟曲霉蛋白的作用,它们与酿酒酵母Pdr5具有高度序列相似性,Pdr5是一种ABC转运蛋白,在这种酵母的唑类抗性分离株中通常过量产生。编码与酿酒酵母Pdr5具有最高序列相似性的ABC转运蛋白的两个烟曲霉基因在这里称为abcA和abcB。我们在三种不同的烟曲霉菌株中构建了这两个不同的ABC转运蛋白编码基因的缺失等位基因。abcB的缺失总是导致唑类敏感性增加,而abcA破坏等位基因具有可变的表型。针对AbcA和AbcB蛋白产生了特异性抗体。这些抗血清允许在野生型细胞中检测到AbcB,而只有当从烟曲霉的hspA启动子过量产生时,AbcA才能可视化。AbcA的过量产生也产生了增加的唑类抗性。绿色荧光蛋白融合用于提供证据,证明AbcA和AbcB都定位于烟曲霉的质膜。与萤火虫荧光素酶的启动子融合表明,两个ABC转运蛋白编码基因的表达都可被唑类挑战诱导。毒力测定表明AbcB是正常发病机制所需的可能因素。这项工作为ABC转运蛋白在这种主要真菌病原体中的生理作用提供了重要的新见解。