Dissemination of IncF group F1:A2:B20 plasmid-harbouring multidrug-resistant Escherichia coli ST131 before the acquisition of blaCTX-M in Japan

被引:9
作者
Hayashi, Michiko [1 ,2 ,5 ]
Matsui, Mari [2 ]
Sekizuka, Tsuyoshi [3 ]
Shima, Ayaka [4 ,6 ]
Segawa, Takaya [4 ,7 ]
Kuroda, Makoto [3 ]
Kawamura, Kumiko [1 ]
Suzuki, Satowa [2 ]
机构
[1] Nagoya Univ, Grad Sch Med, Nagoya, Aichi, Japan
[2] Natl Inst Infect Dis, Antimicrobial Resistance Res Ctr, 4-2-1 Aobachou, Higashimurayama, Tokyo 1890002, Japan
[3] Natl Inst Infect Dis, Pathogen Genom Ctr, Tokyo, Japan
[4] Natl Inst Infect Dis, Dept Bacteriol 2, Tokyo, Japan
[5] Healthcare Syst Co Ltd, Nagoya, Aichi, Japan
[6] Anicom Specialty Med Inst Inc, Tokyo, Japan
[7] Univ Minnesota, Dept Microbiol & Immunol, Minneapolis, MN USA
关键词
Escherichia coli ST131; CTX-M; ESBL; Digestive tract colonization; Plasmid analysis; IncF F1:A2:B20; SEQUENCE TYPE 131; SPECTRUM-CEPHALOSPORIN-RESISTANT; MOLECULAR EPIDEMIOLOGY; H30-RX SUBCLONES; HEALTHY-SUBJECTS; HIGH PREVALENCE; COMMUNITY; VIRULENCE;
D O I
10.1016/j.jgar.2020.10.021
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: The Escherichia coli O25-ST131 clone is responsible for global dissemination of the bla(CTX-M) gene. However, the prevalence of this clone in the digestive tract, devoid of antimicrobial selection, and its molecular epidemiology remain unclear. In this study, we examined the origin of bla(CTX-M)-positive E. coli O25-ST131 and its distribution. Methods: We separately sequenced the chromosomal and plasmid genomes of 50 E. coli O25 isolates obtained from faecal samples of patients with diarrhoea in Japan. Results: Although 36 (72%) of 50 E. coli O25 isolates were ST131, only 6 harboured bla(CTX-M). According to thefimH and ybbW sequences and fluoroquinolone susceptibility, H30R1 isolates were dominant (27/36; 75%) and possessed IncFll-FIA-FIB with FAB formula subtype F1:A2:620 plasmids at a high frequency (24/27; 89%). The F1:A2:620 plasmids possessed more resistance genes such as bla(TEM-1), aminoglycoside resistance genes and trimethoprim/sulfamethoxazole resistance genes compared with non-F1:A2:620 plasmids. In contrast, only one bla(CTX-M-14) gene was located on the F1:A2:620 plasmids, whereas the other three were located on IncEll (F4:A-:B-) (n =1) and IncZ (n = 2) plasmids. Two H30Rx-ST131 isolates harboured bla(CTX-M-15): one was on the chromosome and the other on the IncFIA-R plasmid. The stability and conjugation ability of the F1:A2:620 plasmids were compared with those of non-F1:A2:620 plasmids, which revealed higher stability but lower conjugative ability. Conclusions: These results suggest that E. coli H3OR1-ST131 is a multidrug-resistant clone containing several resistance genes in the F1:A2:620 plasmid, which were widely distributed before the acquisition of bla(CTX-M). (C) 2020 The Author(s). Published by Elsevier Ltd on behalf of International Society for Antimicrobial Chemotherapy.
引用
收藏
页码:456 / 465
页数:10
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