| Project/Area Number |
06557034
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| Research Category |
Grant-in-Aid for Scientific Research (A)
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| Allocation Type | Single-year Grants |
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| Section | 試験 |
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| Research Field |
Legal medicine
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| Research Institution | Mie University |
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Principal Investigator |
FUKUNAGA Tatsushige Faculty of Medicine, Mie University, Professor, 医学部, 教授 (70156800)
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| Co-Investigator(Kenkyū-buntansha) |
NISHI Katsuji Shiga University of Medical Science, Faculty of Medicine, Professor, 医学部, 教授 (60073681)
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| Project Period (FY) |
1994 – 1996
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| Project Status |
Completed (Fiscal Year 1996)
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| Budget Amount *help |
¥7,200,000 (Direct Cost: ¥7,200,000)
Fiscal Year 1996: ¥800,000 (Direct Cost: ¥800,000)
Fiscal Year 1995: ¥900,000 (Direct Cost: ¥900,000)
Fiscal Year 1994: ¥5,500,000 (Direct Cost: ¥5,500,000)
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| Keywords | Plankton / Diatom / Drowning / PCR / ribosomal DNA / Lake Biwa / Picoplankton / Legal Medicine / Legal Medicine / Biwa Lake / Pico plankton |
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| Research Abstract |
A diagnosis of death by drowning is normally based on findings from the external examination of the body and autopsy together with laboratory investigations. The detection of planktons in organs using the chemical digestion method is routinely performed on cadavers for the diagnosis of drowning. In the present study, we attempted to use the molecular biological method for the diagnosis of drowning by PCR analysis of the 16S ribosomal DNA (rDNA) of picoplanktons, belonging to the Synechococcus genus in cyanobacteria (approximately 1 mum in size).
We designed primers complementary to the variable regions of 16S rDNA of the picoplankton we had sequenced.A comparison was made of the PCR products from the three picoplanktons, five other cyanobacteria, Melosira (diatom), Staurasturum (green alga), bacteria from Lake Bikal, and humans. The picogram order of template DNA from picoplankton was specifically amplified by the primers. When the template of picoplankton was mixed with human lung tissue, at least 10 ng of template DNA was needed to obtain a PCR product. The isolation of the picoplankton from lung tissue increased sensitivity of PCR more than a hundred-fold. The specific PCR products of the picoplankton were obtained from formalin-fixed drowning tissue. Molecular biological diagnosis of drowning was successful using picoplankton 16S rDNA.
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