2016 Fiscal Year Annual Research Report
Pathogenic microorganism identification in neonatal infectious diseases by a meta-genomic analysis using the next generation sequencer
| Project/Area Number |
26461632
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| Research Institution | Kobe University |
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Principal Investigator |
森岡 一朗 神戸大学, 医学研究科, 特命教授 (80437467)
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| Co-Investigator(Kenkyū-buntansha) |
池田 真理子 (谷口) 神戸大学, 医学研究科, 特命准教授 (00410738)
竹島 泰弘 神戸大学, 医学研究科, 客員教授 (40281141)
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| Project Period (FY) |
2014-04-01 – 2017-03-31
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| Keywords | 次世代シークエンサー / メタゲノミック診断法 / 周産期・新生児感染症 / 小児感染症 |
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| Outline of Annual Research Achievements |
本研究の目的は、周産期新生児感染症において次世代シークエンサーを用いたメタゲノミック診断法を確立し、今まで同定が困難だった病原微生物の同定を行うことを目指した。
平成26年度に、本研究課題内容に関して神戸大学大学院医学研究科遺伝子解析研究倫理審査委員会の承認を得（no. 104、平成26年9月29日付）、研究のセットアップと、すでに病原微生物を同定できている既存サンプルを用いて、次世代シークエンサーによるメタゲノミック解析（後ろ向き解析）で同定できることを確認した。
平成27年度は、正常分娩であっても、分娩方法の違い（経腟分娩か帝王切開か）によって細菌叢が異なるかを検出するために、患者の同意のもと、種々の分娩方法での胎盤および臍帯を計8検体ずつ収集し解析を試みた。また、先天性細菌感染症発症の胎盤を2検体収集し解析を試みた。さらなる次世代シークエンサーでの解析技術の習得を行った。
平成28年度は、次世代シークエンサー解析技術を含む感染症の病原微生物のゲノム解析を行い、周産期新生児および小児感染症に関連する研究成果発表を行った。
今回の科研費での研究を基に周産期新生児および小児感染症領域の病原微生物を検出するための次世代シークエンサーを用いたメタゲノミック診断法の応用や実用化を目指す。また、藤田保健衛生大学総合医科学研究所分子遺伝学教室倉橋浩樹教授や兵庫県衛生研究所感染症部との共同研究体制も構築できた。
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Research Products
(49 results)
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[Journal Article] Changes in the numbers of patients with acute gastroenteritis after voluntary introduction of the rotavirus vaccine in a Japanese children’s primary emergency medical center.2017
Author(s)
Morioka I, Kamiyoshi N, Nishiyama M, Yamamura T, Minamikawa S, Iwatani S, Nagase H, Nozu K, Nishimura N, Taniguchi-Ikeda M, Ishibashi K, Ishida A, Iijima K
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Journal Title
Environ Health Prev Med.
Volume: 22
Pages: 15
DOI
Peer Reviewed / Open Access / Acknowledgement Compliant
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[Journal Article] Novel missense mutation in DLL4 in a Japanese sporadic case of Adams-Oliver syndrome.2017
Author(s)
Nagasaka M, Taniguchi-Ikeda M, Inagaki H, Ouchi Y, Kuroda D, Yamana K, Harada R, Nozu K, Sakai Y, Morikoka I, Toda T, Kurahashi H, Iijima K
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Journal Title
J Hum Genet.
Volume: 印刷中
Pages: 印刷中
DOI
Peer Reviewed
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[Journal Article] A case of harlequin ichthyosis with a favorable outcome: early treatment and novel, differentially expressed, alternatively spliced transcripts of the ATP-binding cassette sub-family A member 12 gene.2017
Author(s)
Washio K, Sumi M, Nakata K, Fukunaga A, Yamana K, Koda T, Morioka I, Nishigori C, Yamanishi K
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Journal Title
J Dermatol.
Volume: 印刷中
Pages: 印刷中
DOI
Peer Reviewed
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[Journal Article] Characterization of contiguous gene deletions in COL4A6 and COL4A5 in Alport syndrome-diffuse leiomyomatosis.2017
Author(s)
Nozu K, Minamikawa S, Yamada S, Oka M, Yanagita M, Morisada N, Fujinaga S, Nagano C, Gotoh Y, Takahashi E, Morishita T, Yamamura T, Ninchoji T, Kaito H, Morioka I, Nakanishi K, Vorechovsky I, Iijima K
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Journal Title
J Hum Genet.
Volume: 印刷中
Pages: 印刷中
DOI
Peer Reviewed / Int'l Joint Research
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[Journal Article] A birth of bipartite exon by intragenic deletion.2017
Author(s)
Nozu K, Iijima K, Igarashi T, Yamada S, Kralovicova J, Nozu Y, Yamamura T, Minamikawa S, Morioka I, Ninchoji T, Kaito H, Nakanishi K, Vorechovsky I
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Journal Title
Mol Genet Genomic Med.
Volume: 印刷中
Pages: 印刷中
DOI
Peer Reviewed / Open Access / Int'l Joint Research
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[Journal Article] Cryptic exon activation in SLC12A3 in Gitelman syndrome.2017
Author(s)
Nozu K, Nozu Y, Nakanishi K, Konomoto T, Horinouchi T, Shono A, Morisada N, Minamikawa S, Yamamura T, Fujimura J, Nakanishi K, Ninchoji T, Kaito H, Morioka I, Taniguchi-Ikeda M, Vorechovsky I, Iijima K
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Journal Title
J Hum Genet.
Volume: 62
Pages: 335-337
DOI
Peer Reviewed / Int'l Joint Research
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[Journal Article] Rare renal ciliopathies in non-consanguineous families identified by targeted resequencing.2017
Author(s)
Yamamura T, Morisada N, Nozu K, Ishimori S, Toyoshima D, Ninchoji T, Yasui M, Taniguchi-Ikeda M, Morioka I, Nakanishi K, Nishio H, Iijima K
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Journal Title
Clin Exp Nephrol.
Volume: 21
Pages: 136-142
DOI
Peer Reviewed
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[Journal Article] A pediatric patient with interstitial pneumonia due to enterovirus D68.2016
Author(s)
Matsumoto M, Awano H, Ogi M, Tomioka K, Unzaki A, Nishiyama M, Toyoshima D, Taniguchi-Ikeda M, Ishida A, Nagase H, Morioka I, Iijima K
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Journal Title
J Infect Chemother.
Volume: 22
Pages: 712-715
DOI
Peer Reviewed / Acknowledgement Compliant
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[Journal Article] Next generation sequencing discloses a nonsense mutation in the dystrophin gene from long preserved dried umbilical cord and low-level somatic mosaicism in the proband mother.2016
Author(s)
Taniguchi-Ikeda M, Takeshima Y, LeeT, Emoto T, Nishiyama M, Awano H, Yagi M, Unzaki A, Nozu K, Nishio H, Matsuo M, Kurahashi H, Toda T, Morioka I, Iijima K
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Journal Title
J Hum Genet.
Volume: 61
Pages: 351-355
DOI
Peer Reviewed
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[Presentation] Changes in patients with acute gastroenteritis after voluntary introduction of rotavirus vaccine in a Japanese children’s primary emergency medical center.2016
Author(s)
Kamiyoshi N, Iwatani S, Nishiyama M, Yamamura T, Minamikawa S, Taniguchi-Ikeda M, Ishibashi K, Iijima K, Ishida A, Morioka I
Organizer
12nd Congress of Asian Society for Pediatric Research
Place of Presentation
Bangkok, Thailand
Year and Date
2016-11-10 – 2016-11-11
Int'l Joint Research
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[Presentation] A pediatric patient with interstitial pneumonia due to enterovirus D68.2016
Author(s)
Matsumoto M, Awano H, Ogi M, Tomioka K, Unzaki A, Nishiyama M, Toyoshima D, Taniguchi-Ikeda M, Ishida A, Nagase H, Morioka I, Iijima K
Organizer
12nd Congress of Asian Society for Pediatric Research
Place of Presentation
Bangkok, Thailand
Year and Date
2016-11-10 – 2016-11-11
Int'l Joint Research
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[Presentation] Countermeasures against congenital toxoplasmosis and cytomegalovirus infection led by the research team under the supervision of the Ministry of Health, Labor and Welfare in Japan.2016
Author(s)
Fujii T, Ikeda T, Inoue N, Kanayama N, Kawana T, Kimura H, Kobayashi Y, Koyano S, Masuzaki H, Matsuyama H, Minematsu T, Morioka I, Moriuchi H, Oka A, Saito S, Samejima H, Suzutani T, Yamada H, Yoshikawa T
Organizer
CMV Public Health & Policy Conference
Place of Presentation
Austin, Texas, USA
Year and Date
2016-09-26 – 2016-09-27
Int'l Joint Research
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[Presentation] Advantage of next generation sequencing in molecular diagnosis in DMD -mutation screening with long preserved dried umbilical cord and detection of mosaicism-.2016
Author(s)
Taniguchi-Ikeda M, Unzaki A, Takeshima Y, Lee T, Awano H, Yagi M, Kurahashi H, Morioka I, Toda T, Matsuo M, Iijima K
Organizer
13th International Congress of Human Genetics
Place of Presentation
Kyoto, Japan
Year and Date
2016-04-03 – 2016-04-07
Int'l Joint Research
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