Curriculum Vitaes

Yoshichika Arakawa

  (荒川 宜親)

Profile Information

Affiliation
School of Medicine, Fujita Health University
College of Pharmacy, Kinjo Gakuin University
National Institute of Infectious Diseases
Nagoya 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.


Education

 3

Papers

 299
  • Chihiro Norizuki, Yoshichika Arakawa, Jun-ichi Wachino
    Journal of Microbiological Methods, 237 107235-107235, Oct, 2025  Peer-reviewed
  • Sung-Jin Kawai, Shumpei Asamizu, Hiroaki Suzuki, Hiroyasu Onaka, Yoshichika Arakawa, Kouji Kimura, Makoto Ojika
    Journal of Antibiotics(Tokyo), Jul 9, 2025  Peer-reviewed
  • Shogo Otake, Takuya Yamagishi, Takayuki Shiomoto, Manami Nakashita, Hitomi Kurosu, Chiaki Ikenoue, Hirofumi Kato, Munehisa Fukusumi, Tomoe Shimada, Takuri Takahashi, Motoi Suzuki, Teruo Kirikae, Yoshichika Arakawa, Kandai Nozu, Tomimasa Sunagawa, Motoyuki Sugai
    PloS one, 20(8) e0329635, 2025  
    INTRODUCTION: 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.
  • Jayathilake Sarangi, Ayaka Ido, Masaya Ito, Chihiro Iinuma, Yo Doyama, Wanchun Jin, Jun-ichi Wachino, Masahiro Suzuki, Mitsutaka Iguchi, Tetsuya Yagi, Yoshichika Arakawa, Kouji Kimura
    Antimicrobial Agents and Chemotherapy, 68(4) e0117923, Apr 3, 2024  Peer-reviewed
    ABSTRACT 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.
  • Jun-ichi Wachino, Wanchun Jin, Chihiro Norizuki, Kouji Kimura, Motonori Tsuji, Hiromasa Kurosaki, Yoshichika Arakawa
    Microbiology Spectrum, 12(3) e0234423, Feb 5, 2024  
    The 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

Books and Other Publications

 27

Presentations

 108

Teaching 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

 6

Research Projects

 32

Industrial Property Rights

 25

Media Coverage

 1