Emergence of ceftazidime-avibactam resistance in blaKPC-33 -harbouring ST11 Klebsiella pneumoniae in a paediatric patient

被引:3
|
作者
Zhou, Jinlan [1 ]
Yan, Gangfeng [1 ]
Tang, Chengkang [2 ,3 ]
Liu, Jing [1 ]
Fu, Pan [4 ]
Ding, Li [2 ,3 ]
Yang, Weiwei [2 ,3 ]
Guo, Yan [2 ,3 ]
Wang, Chuanqing [4 ]
Lu, Guoping [1 ,5 ]
Hu, Fupin [2 ,3 ]
机构
[1] Fudan Univ, Intens Care Unit, Childrens Hosp, 399 Wanyuan Rd, Shanghai 201102, Peoples R China
[2] Fudan Univ, Inst Antibiot, Huashan Hosp, 12 Urumqi Middle Rd, Shanghai 200040, Peoples R China
[3] Minist Hlth, Key Lab Clin Pharmacol Antibiot, Shanghai, Peoples R China
[4] Fudan Univ, Natl Childrens Med Ctr, Dept Clin Microbiol Lab, Childrens Hosp, Shanghai, Peoples R China
[5] Fudan Univ, Shanghai Inst Infect Dis & Biosecur, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
Paediatric patient; Carbapenem-resistant Klebsiella pneumoniae; KPC-2; KPC-33; Ceftazidime-avibactam; CLINICAL MOLECULAR EPIDEMIOLOGY; ENTEROBACTERIACEAE; INFECTIONS; PHENOTYPE; CHINA;
D O I
10.1016/j.ijantimicag.2024.107163
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Carbapenem-resistant Klebsiella pneumoniae (CRKP) poses immense threats to the health of infected patients worldwide, especially children. This study reports the infection caused by CRKP in a paediatric intensive care unit (PICU) child and its drug-resistant mutation during the treatment. Twelve Klebsiella pneumoniae carbapenemase (KPC)-producing K. pneumoniae strains were isolated from the child. Broth microdilution method, plasmid transformation assay, and whole genome sequencing (WGS) were performed to investigate the antimicrobial susceptibility, resistance mechanisms, and genetic structural features of CRKPs. The results showed that 12 strains were highly resistant to most available antimicrobial agents. Among them, K. pneumoniae FD11 and K. pneumoniae FD12 were resistant to ceftazidime-avibactam (CZA, MIC >64 mg/L) and restored the carbapenem susceptibility (Imipenem, MIC =0.25 mg/L; Meropenem, MIC =2 mg/L). The patient improved after treatment with CZA in combination with aztreonam. Plasmid transformation assay demonstrated that the bla(KPC-33)-positive transformant increased MICs of CZA by at least 33-fold and 8-fold compared with the recipient Escherichia coli DH5 alpha and bla(KPC-2)-positive transformants. WGS analysis revealed that all strains belonged to the ST11-KL64 type and showed highly homologous (3-26 single nucleotide polymorphisms [SNPs]). A single base mutation (G532T) of bla(KPC-2) resulted in a tyrosine to aspartic acid substitution at Ambler amino acid position 179 (D179Y), which conferred CZA resistance in K. pneumoniae. This is the first report of a drug-resistant mutation evolving into bla(KPC-33) during the treatment of bla(KPC-2)-positive CRKP in paediatric-infected patients. It advises clinicians that routine sequential antimicrobial susceptibility testing and KPC genotyping are critical during CZA therapy in children infected with CRKP.<br /> (c) 2024 Elsevier Ltd and International Society of Antimicrobial Chemotherapy.All rights reserved.
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页数:8
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