Laboratory Surveillance for Prospective Plasmid-Mediated AmpC β-Lactamases in the Kinki Region of Japan

Author:

Yamasaki Katsutoshi12,Komatsu Masaru3,Abe Noriyuki4,Fukuda Saori4,Miyamoto Yugo5,Higuchi Takeshi6,Ono Tamotsu7,Nishio Hisaaki8,Sueyoshi Noriyuki9,Kida Kaneyuki10,Satoh Kaori11,Toyokawa Masahiro12,Nishi Isao12,Sakamoto Masako13,Akagi Masahiro14,Nakai Isako15,Kofuku Tomomi16,Orita Tamaki17,Wada Yasunao18,Jikimoto Takumi19,Kinoshita Shohiro19,Miyamoto Kazuaki20,Hirai Itaru2,Yamamoto Yoshimasa2

Affiliation:

1. Department of Clinical Laboratory, Wakayama Rosai Hospital

2. Department of Biomedical Informatics, Osaka University Graduate School of Medicine

3. Department of Technical Section 3, Central Laboratory, FALCO biosystems Ltd

4. Department of Clinical Pathology, Tenri Hospital, Nara

5. Clinical Laboratory, National Hospital Organization Minami Wakayama Medical Center

6. Laboratory for Clinical Investigation, Kyoto University Hospital

7. Clinical Laboratory, Japanese Red Cross Kyoto Daini Hospital, Kyoto

8. Clinical Laboratory, Shiga Medical Center for Adults

9. Clinical Laboratory, Social Insurance Shiga Hospital

10. Clinical Laboratory, Japanese Red Cross Otsu Hospital, Shiga

11. Department of Medical Technology, Kinki University Faculty of Medicine

12. Laboratory for Clinical Investigation, Osaka University Hospital

13. Clinical Laboratory, The Research Foundation for Microbial Diseases of Osaka University

14. Department of Clinical Laboratory, Osaka Police Hospital

15. Clinical Laboratory, Sumitomo Hospital, Osaka

16. Clinical Laboratory, Hyogo Prefectural Nishinomiya Hospital

17. Clinical Laboratory, Takarazuka Municipal Hospital

18. Clinical Laboratory, Hyogo Medical University Hospital

19. Clinical Laboratory, Kobe University Hospital, Hyogo, Japan

20. Department of Microbiology, Wakayama Medical University, School of Medicine, Wakayama

Abstract

ABSTRACT Extended-spectrum β-lactamases, plasmid-mediated AmpC β-lactamases (PABLs), and plasmid-mediated metallo-β-lactamases confer resistance to many β-lactams. In Japan, although several reports exist on the prevalence of extended-spectrum β-lactamases and metallo-β-lactamases, the prevalence and characteristics of PABLs remain unknown. To investigate the production of PABLs, a total of 22,869 strains of 4 enterobacterial species, Escherichia coli , Klebsiella pneumoniae , Klebsiella oxytoca , and Proteus mirabilis , were collected during six 6-month periods from 17 clinical laboratories in the Kinki region of Japan. PABLs were detected in 29 (0.13%) of 22,869 isolates by the 3-dimensional test, PCR analysis, and DNA sequencing analysis. PABL-positive isolates were detected among isolates from 13 laboratories. Seventeen of 13,995 (0.12%) E. coli isolates, 8 of 5,970 (0.13%) K. pneumoniae isolates, 3 of 1,722 (0.17%) K. oxytoca isolates, and 1 of 1,182 (0.08%) P. mirabilis isolates were positive for PABLs. Of these 29 PABL-positive strains, 20 (69.0%), 6 (20.7%), 2 (6.9%), and 1 (3.4%) carried the genes for CMY-2, DHA-1, CMY-8, and MOX-1 PABLs, respectively. Pattern analysis of randomly amplified polymorphic DNA and pulsed-field gel electrophoretic analysis revealed that the prevalence of CMY-2-producing E. coli strains was not due to epidemic strains and that 3 DHA-1-producing K. pneumoniae strains were identical, suggesting their clonal relatedness. In conclusion, the DHA-1 PABLs were predominantly present in K. pneumoniae strains, but CMY-2 PABLs were predominantly present in E. coli strains. The present findings will provide significant information to assist in preventing the emergence and further spread of PABL-producing bacteria.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

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