| Project/Area Number |
15K15383
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| Research Category |
Grant-in-Aid for Challenging Exploratory Research
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| Allocation Type | Multi-year Fund |
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| Research Field |
Infectious disease medicine
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| Research Institution | National Institute of Infectious Diseases |
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Principal Investigator |
Kinjo Yuki 国立感染症研究所, 真菌部, 室長 (20570831)
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| Co-Investigator(Kenkyū-buntansha) |
丸山 徹 熊本大学, 薬学部, 教授 (90423657)
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| Co-Investigator(Renkei-kenkyūsha) |
ISHIMA YU 徳島大学, 大学院医歯薬学研究部, 准教授 (00457590)
UENO KEIGO 国立感染症研究所, 真菌部第三室, 主任研究官 (10550220)
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| Research Collaborator |
SAKAI JUN 国立感染症研究所, 真菌部第三室, 協力研究員
SAITOH NORIKO 国立感染症研究所, 電顕室, 職員
TAKATSUKA SHOGO 国立感染症研究所, 真菌部第三室, 研究員
ABE MASAHIRO 国立感染症研究所, 真菌部第三室, 協力研究員
NAKAHARA MAKIKO 国立感染症研究所, 真菌部第三室, 研究生
KAWAKUBO SHUN 国立感染症研究所, 真菌部第三室, 実習生
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| Project Period (FY) |
2015-04-01 – 2017-03-31
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| Project Status |
Completed (Fiscal Year 2016)
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| Budget Amount *help |
¥3,640,000 (Direct Cost: ¥2,800,000、Indirect Cost: ¥840,000)
Fiscal Year 2016: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2015: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
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| Keywords | 感染症 / 真菌 / 抗真菌薬 / S-ニトロソ化蛋白 / 内科 / 薬学 |
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| Outline of Final Research Achievements |
Invasive fungal infections are associated with high mortality rates. The emergence of drug-resistant fungi is a great concern because of the limited number of antifungal drugs. In this study, we tested antifungal activities of S-nitrosated protein that had been developed as a stable donor of nitric oxide against major fungal pathogens including Candida spp., Cryptococcus spp. and Aspergillus fumigatus. S-nitrosated protein inhibited the growth of these fungi including drug-resistant strains. S-nitrosated protein increased the production of reactive oxygen species and decreased the mitochondrial membrane potential in C. albicans, indicating cell death of this fungus. Furthermore, scanning electron microscopy showed morphological changes in C. albicans upon treatment with this protein. These results demonstrate that S-nitrosated protein has antifungal activities against major fungal pathogens, indicating that this protein is a potential candidate for a new class of antifungal drugs.
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