Synergistic effects of ceftazidime/avibactam combined with meropenem in a murine model of infection with KPC-producing Klebsiella pneumoniae

头孢他啶/阿维巴坦 肺炎克雷伯菌 美罗培南 头孢他啶 微生物学 阿维巴坦 医学 抗药性 碳青霉烯 生物 抗生素 铜绿假单胞菌 细菌 大肠杆菌 抗生素耐药性 遗传学 基因
作者
Mei Zheng,Fu-Hao Li,Juan Liu,Wenjie Li,Ruo-Xi Yin,Da-Tong Cai,Diego O. Andrey,Si-Lin Zheng,Ana Cristina Gales,Wanjiang Zhang,Jian Sun,Xiao‐Ping Liao,Yang Yu
出处
期刊:Journal of Antimicrobial Chemotherapy [Oxford University Press]
卷期号:79 (5): 1069-1080 被引量:1
标识
DOI:10.1093/jac/dkae074
摘要

Abstract Objectives The emergence and expansion of carbapenem-resistant Klebsiella pneumoniae infections is a concern due to the lack of ‘first-line’ antibiotic treatment options. The ceftazidime/avibactam is an important clinical treatment for carbapenem-resistant K. pneumoniae infections but there is an increasing number of cases of treatment failure and drug resistance. Therefore, a potential solution is combination therapies that result in synergistic activity against K. pneumoniae carbapenemase: producing K. pneumoniae (KPC-Kp) isolates and preventing the emergence of KPC mutants resistant to ceftazidime/avibactam are needed in lieu of novel antibiotics. Methods To evaluate their synergistic activity, antibiotic combinations were tested against 26 KPC-Kp strains. Antibiotic resistance profiles, molecular characteristics and virulence genes were investigated by susceptibility testing and whole-genome sequencing. Antibiotic synergy was evaluated by in vitro chequerboard experiments, time-killing curves and dose–response assays. The mouse thigh model was used to confirm antibiotic combination activities in vivo. Additionally, antibiotic combinations were evaluated for their ability to prevent the emergence of ceftazidime/avibactam resistant mutations of blaKPC. Results The combination of ceftazidime/avibactam plus meropenem showed remarkable synergistic activity against 26 strains and restored susceptibility to both the partnering antibiotics. The significant therapeutic effect of ceftazidime/avibactam combined with meropenem was also confirmed in the mouse model and bacterial loads in the thigh muscle of the combination groups were significantly reduced. Furthermore, ceftazidime/avibactam plus meropenem showed significant activity in preventing the occurrence of resistance mutations. Conclusions Our results indicated that the combination of ceftazidime/avibactam plus meropenem offers viable therapeutic alternatives in treating serious infections due to KPC-Kp.
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