Developement of Reverse Genetics for Ibaraki Virus to reveal its replication mechanisms
Project/Area Number |
24780285
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Multi-year Fund |
Research Field |
Basic veterinary science/Basic zootechnical science
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Research Institution | Kobe University |
Principal Investigator |
MATSUO Eiko 神戸大学, (連合)農学研究科(研究院), 助教 (40620878)
|
Research Collaborator |
ROY Polly London School of Hygiene & Tropical Medicine(United Kingdom), 教授
|
Project Period (FY) |
2012-04-01 – 2015-03-31
|
Project Status |
Completed (Fiscal Year 2014)
|
Budget Amount *help |
¥4,550,000 (Direct Cost: ¥3,500,000、Indirect Cost: ¥1,050,000)
Fiscal Year 2014: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2013: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2012: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
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Keywords | 遺伝子改変法 / イバラキウイルス / VP6 / 複製機構 / IBAV / 遺伝子操作系 / 初期複製機構 / リバースジェネティクス / 二本鎖RNAウイルス / ウイルス複製 |
Outline of Final Research Achievements |
Ibaraki virus (IBAV) is a strain of the epizootic hemorrhagic disease virus (EHDV) serogroup, which belongs to the Orbivirus genus of the Reoviridae family. Reverse genetics (RG) system is one of the strong tools to understand molecular mechanisms of virus replication. Here, we developed a RG system for IBAV to identify a nonessential region of a minor structural protein, VP6, by generating VP6-truncated IBAV. Interestingly, the nonessential region of VP6 is sheared in orbiviruses. In addition, several tags were inserted into the truncated region of IBAV VP6 to produce viable VP6-tagged IBAV. We demonstrated that tagged-VP6 proteins were first assembled into puncta in cells infected with VP6-tagged IBAV. Further, as it is believed that orbivirus VP6 is likely to be important for genome packaging, we tried to clarify how orbivirus VP6 could recruit virus genome into the particle by using several orbivirus RG systems.
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Report
(4 results)
Research Products
(23 results)