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Characteristic of KPC-12, a KPC Variant Conferring Resistance to Ceftazidime-Avibactam in the Carbapenem-Resistant Klebsiella pneumoniae ST11-KL47 Clone Background

肺炎克雷伯菌 头孢他啶/阿维巴坦 头孢他啶 微生物学 肉汤微量稀释 生物 质粒 阿维巴坦 碳青霉烯 大肠杆菌 铜绿假单胞菌 抗菌剂 抗生素 最小抑制浓度 基因 细菌 遗传学
作者
Wei Han,Peiyao Zhou,Chun Chen,Chunyang Wu,Ли Шен,Chuanxing Wan,Yang-Hua Xiao,Jiao Zhang,Bingjie Wang,Junhong Shi,Xinru Yuan,Haojin Gao,Hongke Wang,Ying Zhou,Fangyou Yu
出处
期刊:Infection and Drug Resistance [Dove Medical Press]
卷期号:Volume 17: 2541-2554
标识
DOI:10.2147/idr.s465699
摘要

Background: Carbapenem-resistant Klebsiella pneumoniae (CRKP) infections are a great threat to public health worldwide. Ceftazidime-avibactam (CZA) is an effective β -lactam/ β -lactamase inhibitors against CRKP. However, reports of resistance to CZA, mainly caused by Klebsiella pneumoniae carbapenemase (KPC) variants, have increased in recent years. In this study, we aimed to describe the resistance characteristics of KPC-12, a novel KPC variant identified from a CZA resistant K. pneumoniae . Methods: The K. pneumoniae YFKP-97 collected from a patient with respiratory tract infection was performed whole-genome sequencing (WGS) on the Illumina NovaSeq 6000 platform. Genomic characteristics were analyzed using bioinformatics methods. Antimicrobial susceptibility testing was conducted by the broth microdilution method. Induction of resistant strain was carried out in vitro as previously described. The G. mellonella killing assay was used to evaluate the pathogenicity of strains, and the conjugation experiment was performed to evaluate plasmid transfer ability. Results: Strain YFKP-97 was a multidrug-resistant clinical ST11-KL47 K. pneumoniae confers high-level resistance to CZA (16/4 μg/mL). WGS revealed that a KPC variant, KPC-12, was carried by the IncFII (pHN7A8) plasmids (pYFKP-97_a and pYFKP-97_b) and showed significantly decreased activity against carbapenems. In addition, there was a dose-dependent effect of bla KPC-12 on its activity against ceftazidime. In vitro inducible resistance assay results demonstrated that the KPC-12 variant was more likely to confer resistance to CZA than the KPC-2 and KPC-3 variants. Discussion: Our study revealed that patients who was not treated with CZA are also possible to be infected with CZA-resistant strains harbored a novel KPC variant. Given that the transformant carrying bla KPC-12 was more likely to exhibit a CZA-resistance phenotype. Therefore, it is important to accurately identify the KPC variants as early as possible. Keywords: carbapenem-resistant Enterobacterales , Klebsiella pneumoniae , ceftazidime-avibactam, KPC-12, carbapenemase
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