| Project/Area Number |
26660162
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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 |
Aquatic bioproduction science
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| Research Institution | National Institute for Environmental Studies |
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Principal Investigator |
Kodama Keita 国立研究開発法人国立環境研究所, 環境リスク研究センター, 主任研究員 (90391101)
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| Project Period (FY) |
2014-04-01 – 2016-03-31
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| Project Status |
Completed (Fiscal Year 2015)
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| Budget Amount *help |
¥4,030,000 (Direct Cost: ¥3,100,000、Indirect Cost: ¥930,000)
Fiscal Year 2015: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2014: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
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| Keywords | 食性解析 / ペプチド核酸 / 底棲魚介類 / 初期生活史 / 東京湾 / 食性 / 生活史初期 / 甲殻類 |
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| Outline of Final Research Achievements |
We developed a method of PCR-based diet analysis using the peptide nucleic acid (PNA) as a blocking probe for inhibiting DNA amplification of mantis shrimp from Tokyo Bay. We designed universal primers to amplify 28S rDNA for aquatic organisms of a wide range of taxon, and also designed a PNA probe specific to mantis shrimp 28S rDNA. We analyzed DNA template of host (mantis shrimp) and non-host organisms with the universal primers and PNA probe, and confirmed that inhibition of host DNA amplification. PNA-based analysis on samples including stomach and adjacent tissues (e.g., carapace and pleopod) of larvae and juveniles detected potential prey organisms, such as copepods and polychaetes. However, we also detected sequences of non-prey organisms, such as ctenophores whose mucus was attached to the external surface of the host organism. Further modification is required to minimize the effect of non-host contamination, and achieve more efficient detection of prey organisms.
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