Temporal shifts in the predominant carbapenemase gene types among carbapenemase-producing Klebsiella pneumoniae isolated in Bangkok, Thailand, during 2013–2016

Author:

Sakamoto Noriko12,Laolerd Warawut3,Akeda Yukihiro4562,Sugawara Yo21ORCID,Motooka Daisuke7,Yamamoto Norihisa462,Takeuchi Dan2,Shanmugakani Rathina Kumar62,Nishi Isao4,Suzuki Masato1,Shibayama Keigo8,Iida Tetsuya972,Santanirand Pitak3,Tomono Kazunori46,Hamada Shigeyuki2

Affiliation:

1. Antimicrobial Resistance Research Center, National Institute of Infectious Diseases, Tokyo, Japan

2. Japan-Thailand Research Collaboration Center for Infectious Diseases, Research Institute for Microbial Diseases, Osaka University, Osaka, Japan

3. Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand

4. Osaka University Hospital, Osaka University, Osaka, Japan

5. Department of Bacteriology I, National Institute of Infectious Diseases, Tokyo, Japan

6. Department of Infection Control and Prevention, Graduate School of Medicine, Osaka University, Osaka, Japan

7. Department of Infection Metagenomics, Genome Information Center, Research Institute for Microbial Diseases, Osaka University, Osaka, Japan

8. Nagoya University Graduate School of Medicine, Nagoya, Japan

9. Center for Infectious Disease Education and Research, Osaka University, Osaka, Japan

Abstract

Introduction. Carbapenemase-producing Enterobacteriaceae (CPE) have emerged as a global threat to public health and clinical practice. Hypothesis/Gap Statement. In Thailand, reports describing CPEs carrying bla NDM and bla OXA-48-like genes have been increasing recently; however, data on detailed plasmid analysis and temporal shift of sequence type and carbapenemase type are limited. Aim. In this study, we analysed whole-genome sequencing (WGS) data of clinically isolated carbapenemase-producing Klebsiella pneumoniae (CPKP) to reveal the molecular epidemiology of CPKP in a tertiary-care hospital in Bangkok, Thailand. Methodology. Seventy-seven non-duplicated CPKP isolates collected during 2013–2016 were examined for their drug-resistance genes, sequence types and phylogenetic relationships. Results. All the tested isolates possessed carbapenemase gene(s), and the major type of carbapenemase gene in 2014–2015 was bla NDM-1, whereas isolates in 2016 harboured more bla OXA-232 than bla NDM-1. Other carbapenemase gene variants, such as bla NDM-4, bla NDM-5, bla OXA-48, bla OXA-181 and bla IMP-14 were detected in some CPKP isolates. Furthermore, this study revealed that CPKP co-harbouring two genes, bla NDM-1 and bla OXA-232 or bla OXA-181, emerged during this period. Notably, such isolates co-carrying the two carbapenemase genes emerged in three different sequence types, even in a single hospital, and then spread clonally. The WGS of CPKP revealed a temporal shift of the predominant carbapenemase genes from bla NDM-1 to bla OXA-232 along with a variation in other carbapenemase gene types within a span of 4 years. Conclusion. Our findings suggest that a substantial change in CPE types occurred in Thailand and potentially in Southeast Asian countries.

Funder

Japan Agency for Medical Research and Development

Publisher

Microbiology Society

Subject

Microbiology (medical),General Medicine,Microbiology

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