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烟曲霉通过铁载体和铁胺B介导的铁摄取的鉴定

Identification of ferrichrome- and ferrioxamine B-mediated iron uptake by Aspergillus fumigatus.

作者信息

Park Yong-Sung, Kim Ju-Yeon, Yun Cheol-Won

机构信息

School of Life Sciences and Biotechnology, Korea University Anam-dong, Sungbuk-gu, Seoul, Republic of Korea.

School of Life Sciences and Biotechnology, Korea University Anam-dong, Sungbuk-gu, Seoul, Republic of Korea

出版信息

Biochem J. 2016 May 1;473(9):1203-13. doi: 10.1042/BCJ20160066. Epub 2016 Feb 29.

DOI:10.1042/BCJ20160066
PMID:26929401
Abstract

Aspergillus fumigatus is an opportunistic fungal pathogen for immunocompromised patients, and genes involved in siderophore metabolism have been identified as virulence factors. Recently, we identified the membrane transporters sit1 and sit2, which are putative virulence factors of A. fumigatus; sit1 and sit2 are homologous to yeast Sit1, and sit1 and sit2 gene expression was up-regulated after iron depletion. When expressed heterologously in Saccharomyces cerevisiae, sit1 and sit2 were localized to the plasma membrane; sit1 efficiently complemented ferrichrome (FC) and ferrioxamine B (FOB) uptake in yeast cells, whereas sit2 complemented only FC uptake. Deletion of sit1 resulted in a decrease in FOB and FC uptake, and deletion of sit2 resulted in a decrease in FC uptake in A. fumigatus It is of interest that a sit1 and sit2 double-deletion mutant resulted in a synergistic decrease in FC uptake activity. Both sit1 and sit2 were localized to the plasma membrane in A. fumigatus The expression levels of the sit1 and sit2 genes were dependent on hapX under low-but not high-iron conditions. Furthermore, mirB, and sidA gene expression was up-regulated and sreA expression down-regulated when sit1 and sit2 were deleted. Although sit1 and sit2 failed to affect mouse survival rate, these genes affected conidial killing activity. Taken together, our results suggest that sit1 and sit2 are siderophore transporters and putative virulence factors localized to the plasma membrane.

摘要

烟曲霉是免疫功能低下患者的一种机会性真菌病原体,参与铁载体代谢的基因已被确定为毒力因子。最近,我们鉴定了膜转运蛋白sit1和sit2,它们是烟曲霉的假定毒力因子;sit1和sit2与酵母Sit1同源,并且在缺铁后sit1和sit2基因表达上调。当在酿酒酵母中异源表达时,sit1和sit2定位于质膜;sit1有效地补充了酵母细胞中铁色素(FC)和去铁胺B(FOB)的摄取,而sit2仅补充了FC的摄取。在烟曲霉中,sit1的缺失导致FOB和FC摄取减少,sit2的缺失导致FC摄取减少。有趣的是,sit1和sit2双缺失突变体导致FC摄取活性协同降低。在烟曲霉中,sit1和sit2都定位于质膜。在低铁而非高铁条件下,sit1和sit2基因的表达水平依赖于hapX。此外,当sit1和sit2缺失时,mirB和sidA基因表达上调,sreA表达下调。虽然sit1和sit2不影响小鼠存活率,但这些基因影响分生孢子杀伤活性。综上所述,我们的结果表明,sit1和sit2是定位于质膜的铁载体转运蛋白和假定毒力因子。

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