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
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Apr, 2020 - Present
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Apr, 2020 - Mar, 2024
Education
3-
Apr, 1985 - Mar, 1989
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Nov, 1984 - Mar, 1985
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Apr, 1975 - Sep, 1983
Committee Memberships
29-
Oct, 2023 - Present
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Mar, 2022 - Present
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Jul, 2012 - Present
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Apr, 2011 - Present
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Apr, 2005 - Present
Awards
3Papers
299-
Journal of Microbiological Methods, 237 107235-107235, Oct, 2025 Peer-reviewed
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Journal of Antibiotics(Tokyo), Jul 9, 2025 Peer-reviewed
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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.
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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.
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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-
日本臨床, 57(増刊 広範囲血液・尿化学検査 免疫学的検査(3)) 147-149, Nov, 1999
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The Journal of the Japanese Society for Clinical Microbiology, 9(3) 244-250, Sep 25, 1999
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The Japanese Journal of Antibiotics, 52(8) 525-532, Aug, 1999アルベカシン(Arbekacin;ABK)耐性菌43株を対象に,試験を行った.菌学的性状試験によって33株は黄色ブドウ球菌,10株は腸球菌と同定された.ABK耐性は,0.5%食塩含有普通寒天平板にABKを添加して試験した結果,100μg/ml以上の高度耐性を示した株は7株(MRSA2株,腸球菌5株)で,臨床情報の23株と大きく異なった.2つの耐性遺伝子は,黄色ブドウ球菌33株は全てmecA陽性で,うち23株がaac(6')/aph(2")陽性であった.腸球菌はいずれもmecA陰性で,5株がaac(6')/aph(2")陽性であった
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化学療法の領域, 15(9) 1336-1343, Aug, 1999最近,国内で分離された,Klebsiella pneumoniae(K.pneumoniae),Escherichia coli(E.coli),Serratia marcescens(S.marcescens)等の中から第三世代セフェム薬に耐性を示す株を選択し,PCR法による解析を行った.Toho-1,Klebsiella oxytoca(K.oxytoca)の染色体性β-ラクタマーゼに類似のクラスAβ-ラクタマーゼ,AmpC型セファロスポリナーゼ,更にIMP-1型メタロ-β-ラクタマーゼなど,様々なβ-ラクタマーゼを産生している株が混在していることが確認された.また,欧米で問題となっているTEM,SHV由来ESBL産生菌の存在も,複数の国内施設で確認することができた
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Progress in Medicine, 18(11) 2691-2696, Nov, 1998
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小児感染免疫, 10(3) 215-220, Oct, 1998
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臨床検査, 42(11) 1468-1469, Oct, 1998 Lead author
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日本細菌学雑誌, 52(1) 262-262, Jan, 1997
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日本化学療法学会雑誌, 44(補冊A) 106-106, May, 1996
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緑膿菌感染症研究会講演記録, 30回 93-96, Feb, 1996S.marcescens AK9373の例のような,blaIMPとインテグラーゼ遺伝子とアミノ配糖体アセチル化酵素遺伝子の三つのgene cassetteから成るインテグロン構造が,blaIMPが,陽性であるP.aeruginosaの17/24株とS.marcescensの7/12株とK.pneumoniaeで検出された.インテグラーゼ遺伝子はblaIMP陽性のP.aeruginosaの19/24株とS.marcescensの11/12株とK.pneumoniaeで保存されていた.このことから日本全国に,インテグロン構造によってblaIMPのgene cassetteが,異なった菌株の染色体やプラスミド上を転移して,カルバペネム耐性グラム陰性桿菌が伝播しつつあることが示された
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
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創薬支援推進事業, 日本医療研究開発機構(AMED), Apr, 2020 - Mar, 2022
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創薬総合支援事業, 日本医療研究開発機構(AMED), Jan, 2017 - Dec, 2019
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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
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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