Profile Information
- Affiliation
- School of Medicine, Fujita Health UniversityCollege of Pharmacy, Kinjo Gakuin UniversityNational Institute of Infectious DiseasesNagoya University
- Degree
- 医学博士(Mar, 1989, 名古屋大学)
- Researcher number
- 10212622
- J-GLOBAL ID
- 201101032201306103
- Researcher ID
- P-5997-2015
- researchmap Member ID
- 6000030043
In the 1980s, I found that the chromosomal β‐lactamase of Klebsiella pneumoniae
LEN‐1 showed a very high similarity to the R‐plasmid‐mediated penicillinase
TEM‐1 on the amino acid sequence level, and this strongly suggested the origination
of TEM‐1 from the chromosomal penicillinases of K. pneumoniae or related
bacteria. Moreover, the chromosomal K1 β‐lactamase (KOXY) of Klebsiella oxytoca
was found to belong to the class A β‐lactamases that include LEN‐1 and TEM‐1,
although KOXY can hydrolyze cefoperazone (CPZ) like the chromosomal AmpC type
cephalosporinases of various Enterobacteriaceae that can hydrolyze several
cephalosporins including CPZ. Furthermore, my collaborators and I found plural
novel serine‐type β‐lactamases, such as MOX‐1, SHV‐24, TEM‐91, CTX‐M‐64,
CMY‐9, CMY‐19, GES‐3, GES‐4, and TLA‐3, mediated by plasmids. Besides these
serine‐type β‐lactamases, we also first identified exogenously acquired metallo‐
β‐lactamases (MBLs), IMP‐1 and SMB‐1, in imipenem‐resistant Serratia marcescens,
and the IMP‐1‐producing S. marcescens TN9106 became the index case for
carbapenemase‐producing Enterobacteriaceae. I developed the sodium mercaptoacetic
acid (SMA)‐disk test for the simple identification of MBL‐producing
bacteria. We were also the first to identify a variety of plasmid‐mediated 16S
ribosomal RNA methyltransferases, RmtA, RmtB, RmtC, and NpmA, from various
Gram‐negative bacteria that showed very high levels of resistance to a wide
range of aminoglycosides. Furthermore, we first found plasmid‐mediated quinolone
efflux pump (QepA) and fosfomycin‐inactivating enzymes (FosA3 and FosK).
We also first characterized penicillin reduced susceptible Streptococcus agalactiae (PRGBS),
macrolide‐resistant Mycoplasma pneumoniae, as well as Campylobacter jejuni, and
Helicobacter pylori, together with carbapenem‐resistant Haemophilus influenzae.
Research Interests
2Research Areas
3Major Research History
30-
Apr, 2020 - Present
-
Apr, 2020 - Present
-
Apr, 2020 - Mar, 2024
Education
3-
Apr, 1985 - Mar, 1989
-
Nov, 1984 - Mar, 1985
-
Apr, 1975 - Sep, 1983
Committee Memberships
29-
Oct, 2023 - Present
-
Mar, 2022 - Present
-
Jul, 2012 - Present
-
Apr, 2011 - Present
-
Apr, 2005 - Present
Awards
3Papers
299-
Journal of Microbiological Methods, 237 107235-107235, Oct, 2025 Peer-reviewed
-
Journal of Antibiotics(Tokyo), Jul 9, 2025 Peer-reviewed
-
PloS one, 20(8) e0329635, 2025INTRODUCTION: Antimicrobial resistance in Pseudomonas aeruginosa is one of the global health concerns. Like many countries, Japan monitors multidrug-resistant P. aeruginosa (MDRP) infections through a national sentinel surveillance system, which has shown a recent decline in MDRP reports. We evaluated this surveillance system to verify the validity of this trend and explore future directions. METHODS: We conducted a cross-sectional mixed-method study based mainly on the guidelines published by the United States Centers for Disease Control and Prevention in 2001. As a quantitative method, we analyzed characteristics of reports on MDRP infections from designated sentinel sites (DSSs) between 2013-2022. A questionnaire was sent to identifiable DSSs (target DSSs) requesting data on accurate numbers of MDRP infections between 2018-2022 to assess attributes such as geographical representativeness. Additionally, we conducted as a qualitative method face-to-face, semi-structured key informant interviews with surveillance system stakeholders to assess its usefulness and challenges. RESULTS: From 2013 to 2022, 1,666 cases of MDRP infections were reported by 463 target DSSs, which were scattered across the county. We obtained valid responses to the questionnaire survey from 231 target DSSs (49.9%). From 2018 to 2022, these sites reported 277 cases as MDRP infections, while 184 cases were accurate cases of MDRP infection, with both numbers declining over time. False reporting and underreporting of MDRP infections were common, resulting in a positive predictive value of 0.45 and a sensitivity of 0.65 for the reports of MDRP infections to the surveillance system. The interviews highlighted the difficulties in timely detection, accurate reporting, and international data comparison. CONCLUSION: Our evaluation indicated that the current sentinel surveillance system for MDRP infections partially captured the true decreasing trend in Japan. However, as the epidemiology of drug-resistant P. aeruginosa is changing, national policy and surveillance strategies would need to address changing public health needs.
-
Antimicrobial Agents and Chemotherapy, 68(4) e0117923, Apr 3, 2024 Peer-reviewedABSTRACT Streptococcus mitis/oralis group isolates with reduced carbapenem susceptibility have been reported, but its isolation rate in Japan is unknown. We collected 356 clinical α-hemolytic streptococcal isolates and identified 142 of them as S. mitis/oralis using partial sodA sequencing. The rate of meropenem non-susceptibility was 17.6% (25/142). All 25 carbapenem-non-susceptible isolates harbored amino acid substitutions in/near the conserved motifs in PBP1A, PBP2B, and PBP2X. Carbapenem non-susceptibility is common among S. mitis/oralis group isolates in Japan.
-
Microbiology Spectrum, 12(3) e0234423, Feb 5, 2024The number and type of metallo-β-lactamase (MΒL) are increasing over time. Carbapenem resistance conferred by MΒL is a significant threat to our antibiotic regimen, and the development of MΒL inhibitors is urgently required to restore carbapenem efficacy. Microbial natural products have served as important sources for developing antimicrobial agents targeting pathogenic bacteria since the discovery of antibiotics in the mid-20th century. MΒL inhibitors derived from microbial natural products are still rare compared to those derived from chemical compound libraries. Hydroxyhexylitaconic acids (HHIAs) produced by members of the genus Aspergillus have potent inhibitory activity against clinically relevant IMP-type MBL. HHIAs may be good lead compounds for the development of MBL inhibitors applicable for controlling carbapenem resistance in IMP-type MBL-producing Enterobacterales .
Misc.
1124-
結核等抗酸菌感染症における生体防御及び抗菌制御を介した治療予防法の開発戦略 平成23年度 総括・分担研究報告書, 17-20, 2012
-
第40回 薬剤耐性菌研究会 【シンポジウムI】<耐性菌の疫学・サーベイランス・感染制御>(2011年12月1日-2日:伊香保), Dec, 2011
-
第40回 薬剤耐性菌研究会発表抄録集【シンポジウムI】 <耐性菌の疫学・サーベイランス・感染制御> (2011年12月1日-2日:伊香保), Dec, 2011
-
第40回 薬剤耐性菌研究会発表抄録集 (2011年12月1日-2日:伊香保), Dec, 2011
-
第40回 薬剤耐性菌研究会発表抄録集 (2011年12月1日-2日:伊香保), Dec, 2011
-
第40回 薬剤耐性菌研究会【シンポジウムI】<耐性菌の疫学・サーベイランス・感染制御>(2011年12月1日-2日:伊香保), Nov, 2011
-
福井県衛生環境研究センター年報, 9 33-37, Nov, 2011平成21年から平成22年に福井市内で購入した国内産鶏肉66検体中23検体から分離された30株および散発下痢症患者から分離された27株のCTX-M型基質特異性拡張型β-ラクタマーゼ(ESBL)産生大腸菌の分子疫学的性状を比較検討した。最も多かった血清型は鶏肉由来株でO78:H9、ヒト由来株でO25:H4であった。鶏肉とヒトの両方で確認された血清型はO78:H9およびO25:HNMの2種類であった。鶏肉由来およびヒト由来のO78:H9の各1株は、CTX-M型はCTX-M-55、系統発生群はA、パルスフィールドゲル電気泳動パターンは類似し、MIC値はセフピロム以外がほぼ一致した。CTX-M-15型、シークエンスタイプが131、系統発生群がB2、シプロフロキサシン耐性を示すO25:H4がヒトから分離された。
-
IUMS2011 Sapporo; Abstract, 242-242, Sep 10, 2011 Last author
-
IUMS2011 Sapporo; Abstract, 222-222, Sep 9, 2011
-
IUMS2011 Sapporo: Abstract, 221-221, Sep 9, 2011 Last author
-
IUMS 2011 Sapporo; Abstract, 151-151, Sep 7, 2011 Last author
-
小児科診療, 74(9) 1315-1321, Sep, 2011 Lead author
-
SRL宝函, 32(2) 24-32, Jul, 2011カルバペネム耐性菌は、メタロ-β-ラクタマーゼ(MBL)、OXA型カルバペネマーゼ、KPC型カルバペネマーゼを産生するタイプが代表的である。2010年にNDM-1と命名された新型のMBLを産生する多剤耐性肺炎桿菌は全世界に広がりをみせている。新型の多剤耐性グラム陰性桿菌には有効な抗菌薬が殆どなく、血流中に侵入すると致命的である。その対策として、サーベイランスデータの活用、早期検出、伝播防止対策の徹底、情報共有が必要である。
-
日本化学療法学会雑誌, 59(Suppl.A) 189-189, Jun, 2011
-
日本環境感染学会総会プログラム・抄録集, 26回 165-165, Feb, 2011
-
結核等抗酸菌感染症における生体防御及び抗菌制御を介した治療予防法の開発戦略 平成22年度 総括・分担研究報告書, 15-20, 2011
Books and Other Publications
27Presentations
108Teaching Experience
1-
1989 - Present医学細菌学、病原細菌学、薬剤耐性菌等 (名古屋大学 [医、保健、工]、群馬大学 [医]、千葉大学 [薬]、東京薬科大学 [薬]、愛知学院大学 [歯・薬]、岐阜薬科大学 [薬]、愛知医科大学[医]、 他)
Professional Memberships
6Research Projects
32-
創薬支援推進事業・創薬総合支援事業, 日本医療研究開発機構(AMED), Apr, 2022 - Mar, 2025
-
創薬支援推進事業, 日本医療研究開発機構(AMED), Apr, 2020 - Mar, 2022
-
創薬総合支援事業, 日本医療研究開発機構(AMED), Jan, 2017 - Dec, 2019
-
感染症実用化研究事業, 日本医療研究開発機構(AMED), Apr, 2016 - Mar, 2019
-
感染症研究国際展開戦略プログラム(J-GRID), 日本医療研究開発機構(AMED), Oct, 2015 - Mar, 2018