111 research outputs found

    西部北太平洋における溶存酸素の長期および周期変動に関する研究

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    この博士論文は全文公表に適さないやむを得ない事由があり要約のみを公表していましたが、解消したため、令和2(2020)年6月1日に全文を公表しました。筑波大学 (University of Tsukuba)201

    Dissolved methane distribution in surface seawater and its controlling factors  in mid- and high-latitudes in the Southern Ocean

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    第6回極域科学シンポジウム分野横断セッション:[IB1] 海氷域における生物地球化学的研究11月17日(火) 統計数理研究所 セミナー室1(D305

    Trends and decadal oscillations of oxygen and nutrients at 50 to 300m depth in the equatorial and North Pacific

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    A strong oxygen-deficient layer is located in the upper layers of the tropical Pacific Ocean and deeper in the North Pacific. Processes related to climate change (upper-ocean warming, reduced ventilation) are expected to change ocean oxygen and nutrient inventories. In most ocean basins, a decrease in oxygen (“deoxygenation”) and an increase in nutrients have been observed in subsurface layers. Deoxygenation trends are not linear and there could be multiple influences on oxygen and nutrient trends and variability. Here oxygen and nutrient time series since 1950 in the Pacific Ocean were investigated at 50 to 300 m depth, as this layer provides critical pelagic habitat for biological communities. In addition to trends related to ocean warming the oxygen and nutrient trends show a strong influence of the Pacific Decadal Oscillation (PDO) in the tropical and the eastern Pacific, and the North Pacific Gyre Oscillation (NPGO) in particular in the North Pacific. In the Oyashio Region the PDO, the NPGO, the North Pacific Index (NPI) and an 18.6-year nodal tidal cycle overlay the long-term trend. In most eastern Pacific regions oxygen increases and nutrients decrease in the 50 to 300 m layer during the negative PDO phase, with opposite trends during the positive PDO phase. The PDO index encapsulates the major mode of sea surface temperature variability in the Pacific, and oxygen and nutrients trends throughout the basin can be described in the context of the PDO phases. El Niño and La Niña years often influence the oxygen and nutrient distribution during the event in the eastern tropical Pacific but do not have a multi-year influence on the trends

    Molecular Serotype-Specific Identification of Non-Type B \u3cem\u3eHaemophilus influenzae\u3c/em\u3e by Loop-Mediated Isothermal Amplification

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    In children, the incidence of pneumococcal meningitis has decreased since the introduction of pneumococcal conjugate vaccine (PCV7 and PCV13). However, since the introduction of the vaccine, developed countries have seen the emergence of non-PCV13 serotypes. However, invasive pneumococcal disease (IPD) caused by PCV13-targeted serotypes still represents an important public health problem in resource-limited countries. To develop a rapid, simple, and cost-effective assay to detect serotypes of Streptococcus pneumoniae, we developed a novel loop-mediated isothermal amplification (LAMP) assay based on the sequences available for the 13 capsular types that are included in PCV13: 1, 3, 4, 5, 6 A, 6B, 7 F, 9 V, 14, 18 C, 19 A, 19 F, and 23 F. We evaluated test reactivity, specificity, sensitivity and performance, and compared the results between established LAMP and conventional PCR assays. To support its clinical use, the detection limits of the LAMP assay were evaluated using bacterial genomic DNA-spiked cerebrospinal fluid (CSF) and blood specimens. We confirmed the specificity of the LAMP assay using 41 serotypes of pneumococcal strains. The sensitivity of the LAMP assay was 10 to 100 copies per reaction, compared to 10 to 104 copies per reaction for PCR assays. The detection limits of the LAMP assay were comparable when using DNA-spiked CSF and blood specimens, as compared to using purified DNA as the template. In conclusion, a rapid and simple LAMP-based pneumococcal serotyping method has been developed. This is the first report of a LAMP method for a PCV13 serotype-specific identification assay, which could be a promising step to facilitate epidemiological studies of pneumococcal serotyping

    南大洋110E度線の季節海氷域におけるpCO2の変動

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    第6回極域科学シンポジウム分野横断セッション:[IB1] 海氷域における生物地球化学的研究11月17日(火) 国立極地研究所1階交流アトリウ

    表層海水中溶存酸素の高精度連続観測

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    大気・海洋間の二酸化炭素や酸素の交換量と,その時空間変動要因や,大気中の温室効果ガスの動態を解明するための一環として,表層海水中溶存酸素の高精度連続観測に取り組んでいる.海洋地球研究船「みらい」では,表層海水連続測定装置により,水温・塩分の測定に加え,世界中で広く利用されているAADI社製OPTODEによる溶存酸素,および,蛍光光度計によるクロロフィルaの測定が行われてきた.OPTODEは時間安定性が優れており,連続観測に適していると考えられているが,応答時間が遅い(カタログによれば67%応答時間は20℃で23秒)という問題があった.そこで,船舶CTDO観測で培った高精度溶存酸素測定技術に基づき,2012年度から表層海水連続測定装置に応答時間が早いJFE Advantech社製RINKOを追加した.溶存酸素検出膜の適切なエイジングと標準ガスを用いたセンサー出力値の線形化,および,時間ドリフト補正用の溶存酸素の分析値を取得することで,溶存酸素の高精度連続観測を実現し,北極海,ベーリング海,西部太平洋,南大洋の広範囲でデータを蓄積した.従来のOPTODEと新たに導入したRINKOの比較から,RINKOに比べてOPTODEは約8分遅れて応答していることや,北極海などでの塩分の短時間での大きな変化に対応してOPTODEが不自然に大きく応答することが明らかになった.さらに,RINKOの技術を応用し,センサーを用いた酸素法による基礎生産量の測定を試みている.これらのデータを総合的に解析し,表層海水中の溶存酸素の時空間変動特性を把握し,変動要因の解明を目指す.BE13-19講演要旨 / ブルーアース2013(2013年3月14日~15日, 東京海洋大学品川キャンパス)http://www.godac.jamstec.go.jp/darwin/cruise/mirai/mr12-e03/

    DOCK2 is involved in the host genetics and biology of severe COVID-19

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    「コロナ制圧タスクフォース」COVID-19疾患感受性遺伝子DOCK2の重症化機序を解明 --アジア最大のバイオレポジトリーでCOVID-19の治療標的を発見--. 京都大学プレスリリース. 2022-08-10.Identifying the host genetic factors underlying severe COVID-19 is an emerging challenge. Here we conducted a genome-wide association study (GWAS) involving 2, 393 cases of COVID-19 in a cohort of Japanese individuals collected during the initial waves of the pandemic, with 3, 289 unaffected controls. We identified a variant on chromosome 5 at 5q35 (rs60200309-A), close to the dedicator of cytokinesis 2 gene (DOCK2), which was associated with severe COVID-19 in patients less than 65 years of age. This risk allele was prevalent in East Asian individuals but rare in Europeans, highlighting the value of genome-wide association studies in non-European populations. RNA-sequencing analysis of 473 bulk peripheral blood samples identified decreased expression of DOCK2 associated with the risk allele in these younger patients. DOCK2 expression was suppressed in patients with severe cases of COVID-19. Single-cell RNA-sequencing analysis (n = 61 individuals) identified cell-type-specific downregulation of DOCK2 and a COVID-19-specific decreasing effect of the risk allele on DOCK2 expression in non-classical monocytes. Immunohistochemistry of lung specimens from patients with severe COVID-19 pneumonia showed suppressed DOCK2 expression. Moreover, inhibition of DOCK2 function with CPYPP increased the severity of pneumonia in a Syrian hamster model of SARS-CoV-2 infection, characterized by weight loss, lung oedema, enhanced viral loads, impaired macrophage recruitment and dysregulated type I interferon responses. We conclude that DOCK2 has an important role in the host immune response to SARS-CoV-2 infection and the development of severe COVID-19, and could be further explored as a potential biomarker and/or therapeutic target
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