The comprehensive study of bacterial IpaH family effectors
Project/Area Number |
25460527
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Bacteriology (including mycology)
|
Research Institution | The University of Tokyo |
Principal Investigator |
Ashida Hiroshi 東京大学, 医科学研究所, 特任准教授 (10535115)
|
Project Period (FY) |
2013-04-01 – 2016-03-31
|
Project Status |
Completed (Fiscal Year 2015)
|
Budget Amount *help |
¥5,200,000 (Direct Cost: ¥4,000,000、Indirect Cost: ¥1,200,000)
Fiscal Year 2015: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2014: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Fiscal Year 2013: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
|
Keywords | 赤痢菌 / エフェクター / 自然免疫 / I型インターフェロン |
Outline of Final Research Achievements |
In this study, we tried to identify the mechanism of IpaH family effector proteins, which have E3 ubiquitin ligase activity, in Shigella infection. One of IpaH family protein, IpaH0722 inhibits NF-κB activity in its E3 ubiquitin ligase dependent manner. As a result, we found that IpaH0722 inhibits phagosome disruption mediated PKC-NF-κB activation by targeting TRAF2 for ubiquitination and proteasome-dependent degradation, thereby downregulating host inflammatory responses.In addition, another IpaH family protein, IpaH5 inhibits DNA dependent type I interferon signaling by targeting signaling factor X for ubiquitination.
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Report
(4 results)
Research Products
(15 results)