4.2 Article

In vitro antibacterial effects of Tanreqing injection combined with vancomycin or linezolid against methicillin-resistant Staphylococcus aureus

期刊

出版社

BMC
DOI: 10.1186/s12906-018-2231-8

关键词

Tanreqing; Vancomycin; Linezolid; Methicillin-resistant Staphylococcus aureus; MRSA; Synergistic effect; Biofilm

资金

  1. National Natural Sciences Foundation of China [81373884]
  2. Basic Scientific Research Fund from Ministry of Finance of China [Y201701, ZZ0808011, ZZ2014004]
  3. National Natural Sciences Foundation of Beijing [7132157]
  4. Bilateral Cooperation Project Croatia-China - Ministry of Science & Technology of the People's Republic of China
  5. Ministry of Science and Education of the Republic of Croatia [7-10]

向作者/读者索取更多资源

Background: Combining conventional drugs and traditional medicine may represent a useful approach to combating antibiotic resistance, which has become a serious threat to global public health. This study aimed to evaluate the potential synergistic interactions between Tanreqing (TRQ) injection, a commercial traditional Chinese medicine formula used for the treatment of upper respiratory tract infection, and selected antibiotics used against methicillin-resistant Staphylococcus aureus (MRSA). Methods: The minimum inhibitory concentrations (MICs) of TRQ, vancomycin and linezolid against planktonic MRSA strain were determined by the broth microdilution method. The combined effects of TRQ and antibiotics were studied by the checkerboard method and the time-kill curve assay. The 2,3-bis-(2-methoxy-4-nitro-5-sulfophenyl)-2H-tetrazolium5-carboxanilide (XTT) reduction assay was employed to determine the inhibitory effect of the test compounds alone and in combination against MRSA embedded in biofilms. Results: MRSA strain was found to be susceptible to TRQ formula with MIC value 4125 mu g/ml, while the MIC values for antibiotics, vancomycin and linezolid, were 2.5 mu g/ml. The checkerboard analysis revealed that TRQ markedly enhanced activities of the tested antibiotics by reducing their MICs. In the time-kill analysis, TRQ at 1/2 xMIC in combination with vancomycin at 1/2 xMIC, as well as TRQ at 1/8 xMIC in combination with linezolid at 1/2 xMIC decreased the viable colonies by >= 2log10 CFU/ml, resulting in a potent synergistic effect against planktonic MRSA. In contrast to the tested antibiotics, which did not affect mature MRSA biofilms at subinhibitory concentrations, TRQ alone showed strong ability to disrupt preformed biofilms and induce biofilm cell death. The combination of TRQ with vancomycin or linezolid at sub-MIC concentrations resulted in a synergistic antibiofilm effect significantly higher than for each single agent. Conclusions: This study provides the first in vitro evidence on the synergistic effects of TRQ and vancomycin or linezolid against planktonic and biofilm MRSA, and revealed their optimal combination doses, thereby providing a rational basis for the combination therapies against MRSA.

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