2022 Fiscal Year Final Research Report
Pathogenesis of invasive infections caused by non typeable H. influenzae.
Project/Area Number |
20K08244
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Review Section |
Basic Section 52050:Embryonic medicine and pediatrics-related
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Research Institution | Kurume University |
Principal Investigator |
Gotoh Kenji 久留米大学, 医学部, 講師 (90572313)
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Co-Investigator(Kenkyū-buntansha) |
多々良 一彰 久留米大学, 医学部, 助教 (30839006)
田中 悠平 久留米大学, 医学部, 助教 (70446102)
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Project Period (FY) |
2020-04-01 – 2023-03-31
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Keywords | 侵襲性インフルエンザ菌感染症 / 無莢膜型インフルエンザ菌 / バイオフィルム |
Outline of Final Research Achievements |
Strains isolated from invasive infections caused by non-capsular influenza (NTHi) bacteria infections had a higher biofilm-producing capacity compared to strains isolated from the respiratory tract. Strains isolated from bacterial meningitis in neonates did not show biofilm production. The results suggest that the pathogenesis of invasive infections in neonates and children differs. Structural analysis of biofilms showed that strains causing invasive infections had extracellular DNA covering their surfaces, in which a large number of viable bacteria were present, whereas strains of respiratory origin produced biofilms but had less extracellular DNA. Expression analysis of the HI1296 gene was performed to confirm this phenomenon, but again, the expression of the gene was higher in strains derived from invasive infections.
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Free Research Field |
小児感染症 予防接種 感染制御学
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Academic Significance and Societal Importance of the Research Achievements |
小児だけでなく成人においても増加傾向にある侵襲性インフルエンザ菌感染症の病態解明の糸口になると考えられる。我々の研究結果からバイフィルムの解析に基づき治療戦略や予防法の確立に貢献できると考えられる。また、これらの菌株の分子生物学的特徴も明らかにできれば菌株の早期発見を行うことができ、感染症が起こった時の早期介入も可能となり治療成績の向上に貢献できると考えられる。
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