In vitro and in vivo synergistic effects of tigecycline combined with aminoglycosides on carbapenem-resistant Klebsiella pneumoniae

被引:19
|
作者
Ni, Wentao [1 ]
Yang, Deqing [2 ,3 ]
Guan, Jie [4 ]
Xi, Wen [1 ]
Zhou, Dexun [1 ]
Zhao, Lili [1 ]
Cui, Junchang [5 ]
Xu, Yu [1 ]
Gao, Zhancheng [1 ]
Liu, Youning [5 ]
机构
[1] Peking Univ, Dept Pulm & Crit Care Med, Peoples Hosp, Beijing 100044, Peoples R China
[2] Sichuan Univ, West China Hosp, Div Pulm Dis, State Key Lab Biotherapy China, Chengdu 610041, Peoples R China
[3] Sichuan Univ, Dept Resp & Crit Care Med, West China Hosp, Chengdu 610041, Peoples R China
[4] Peking Univ, Clin Lab, Hosp 1, Beijing 100034, Peoples R China
[5] Chinese Peoples Liberat Army Gen Hosp, Dept Resp Dis, Beijing 100853, Peoples R China
基金
中国国家自然科学基金;
关键词
CRITICALLY-ILL PATIENTS; ENTEROBACTERIACEAE; PHARMACOKINETICS; GENTAMICIN; AMIKACIN; EFFICACY;
D O I
10.1093/jac/dkab122
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: Carbapenem-resistant Klebsiella pneumoniae (CR-KP) infections represent severe threats to public health worldwide. The aim of this study was to assess potential synergistic interaction between tigecycline and aminoglycosides via in vitro and in vivo studies. Methods: Antibiotic resistance profiles and molecular characteristics of 168 CR-KP clinical isolates were investigated by susceptibility testing, PCR and MLST. Chequerboard tests and time-kill assays were performed for 20 CR-KP isolates to evaluate in vitro synergistic effects of tigecycline combined with aminoglycosides. A tissuecage infection model of rats was established to evaluate in vivo synergistic effects. Different doses of tigecycline and aminoglycosides alone or in combination were administered for 7 days via tail vein injection. Antibiotic efficacy was evaluated in tissue-cage fluid and emergence of resistance was screened. Results: The chequerboard tests showed that this combination displayed synergistic or partial synergistic activity against CR-KP. The time-kill assays further demonstrated that strong synergistic effects of such a combination existed against isolates that were susceptible to both drugs but for resistant isolates no synergy was observed if clinical pharmacokinetics were taken into consideration. The in vivo study showed that the therapeutic effectiveness of combination therapies was better than that of monotherapy for susceptible isolates, suggesting in vivo synergistic effects. Furthermore, combinations of tigecycline with an aminoglycoside showed significant activity in reducing the occurrence of tigecycline-resistant mutants. Conclusions: Compared with single drugs, tigecycline combined with aminoglycosides could exert synergistic effects and reduce theemergence of tigecycline resistance. Such a combination might be an effective alternative when treating CR-KP infections in clinical practice.
引用
收藏
页码:2097 / 2105
页数:9
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