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International Journal of Clinical & Medical Microbiology Volume 3 (2018), Article ID 3:IJCMM-136, 4 pages
https://doi.org/10.15344/2456-4028/2018/136
Research Article
Whole Genome Sequence Analysis of CTX-M-55 Producing Escherichia coli Isolates from Clinical Patients in Japan

Yuya Hasunuma1,*, Moe Yokemura1, Nozomi Hiyoshi1, Takashi Ishimatsu2, Takuya Tsunoda2, Satoshi Kugawa2 and Yoshikazu Tokuoka1

1Graduate School of Engineering, Toin University of Yokohama, Kurogane-cho, Aoba-ku, Yokohama, Kanagawa, Japan
2Health Sciences Research Institute, Toin University of Yokohama, Godo-cho, Hodogaya-ku, Yokohama, Kanagawa, Japan
Dr. Yuya Hasunuma, Graduate School of Engineering, Toin University of Yokohama, 1614 Kurogane-cho, Aoba-ku, Yokohama, Kanagawa 225-8503, Japan, Tel: +81-45-972-5881; E-mail: hyuya@toin.ac.jp
06 November 2018; 10 December 2018; 12 December 2018
Hasunuma Y, Yokemura M, Hiyoshi N, Ishimatsu T, Tsunoda T, et al. (2018) Whole Genome Sequence Analysis of CTX-M-55 Producing Escherichia coli Isolates from Clinical Patients in Japan. Int J Clin Med Microbiol 3: 136. doi: https://doi.org/10.15344/2456-4028/2018/136

Abstract

Extended-spectrum β-lactamase (ESBL) producing Escherichia coli is one of the most important drug resistant pathogen of clinical infection and is of global concern. CTX-M-55 type ESBL that has D240G amino acid substitution to confer ceftazidime resistance is often isolated from not only clinical patients, but also livestocks and retail meats. This study revealed molecular epidemiology and characteristics of CTX-M-55 producing E. coli isolated from medical facilities in Japan with less than 300 beds. Among the isolates possessing blaCTX-M-55, antimicrobial susceptibility was examined, and resistant genes, sequence type, and incompatibility type of its plasmids were determined by next-generation sequencing. The proportion of E. coli harboring blaCTX-M-55 ESBL was 12.5% (8/64) of the CTX-M-1 group ESBL genes positive isolates. Four and six isolates were resistant to fosfomycin and ciprofloxacin, respectively. Results of the whole genome sequencing for blaCTX-M-55 positive strains, sequence type and plasmid incompatibility were dominant as ST131 and IncF, respectively. Further, two isolates determind as ST131 were likely to be isolated from the same facility, and are identical. This finding suggests that continuous surveillance for CTX-M-55 producing E. coli ST131 is needed. Moreover, the presence of floR gene in clinical strain implied that ingestion of contaminated meat and/or contact of livestocks transferred CTX-M-55 producing E. coli to community human. Additionally, the spread of fosA possessing E. coli combined with blaCTX-M-55 may restrict therapeutic options against patients of urinary tract infection on which β-lactam has no therapeutic effect. In conclusion, this is the first study on the epidemiology and characteristics of CTX-M-55 ESBL producing E. coli isolates from regional medical facilities with less than 300 beds in Japan. These results show that CTX-M-55 producing E. coli originates from a different clone such as pandemic and veterinary clone.