4.7 Article

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

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JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY
卷 76, 期 8, 页码 2097-2105

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OXFORD UNIV PRESS
DOI: 10.1093/jac/dkab122

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资金

  1. National Natural Science Foundation of China [81903672]
  2. Peking University People's Hospital Research and Development Funds [RDY2018-14]
  3. Ministry of Science and Technology of China [2017ZX10103004-006]

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The study found synergistic or partial synergistic activity between tigecycline and aminoglycosides against CR-KP. Combination therapies showed better therapeutic effectiveness compared to monotherapy for susceptible isolates, indicating in vivo synergistic effects. Additionally, the combination of tigecycline with an aminoglycoside significantly reduced the occurrence of tigecycline-resistant mutants.
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.

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