| Literature DB >> 29170805 |
Xiaodong Jia1, Xi Zhang1, Yingsong Hu1, Mandong Hu1, Shuguang Tian1, Xuelin Han1, Yansong Sun2, Li Han3.
Abstract
Aspergillus fumigatus is a major fungal pathogen that is responsible for approximately 90% of human aspergillosis. Cofilin is an actin depolymerizing factor that plays crucial roles in multiple cellular functions in many organisms. However, the functions of cofilin in A. fumigatus are still unknown. In this study, we constructed an A. fumigatus strain overexpressing cofilin (cofilin OE). The cofilin OE strain displayed a slightly different growth phenotype, significantly increased resistance against H2O2 and diamide, and increased activation of the high osmolarity glycerol pathway compared to the wild-type strain (WT). The cofilin OE strain internalized more efficiently into lung epithelial A549 cells, and induced increased transcription of inflammatory factors (MCP-1, TNF-α and IL-8) compared to WT. Cofilin overexpression also resulted in increased polysaccharides including β-1, 3-glucan and chitin, and increased transcription of genes related to oxidative stress responses and polysaccharide synthesis in A. fumigatus. However, the cofilin OE strain exhibited similar virulence to the wild-type strain in murine and Galleria mellonella infection models. These results demonstrated for the first time that cofilin, a regulator of actin cytoskeleton dynamics, might play a critical role in the regulation of oxidative stress responses and cell wall polysaccharide synthesis in A. fumigatus.Entities:
Keywords: Aspergillus fumigatus; Cell wall polysaccharides; Cofilin; Inflammatory response; Oxidative stress resistance
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Year: 2017 PMID: 29170805 DOI: 10.1007/s00294-017-0777-5
Source DB: PubMed Journal: Curr Genet ISSN: 0172-8083 Impact factor: 3.886