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  • 學位論文

CX加強抗生素對革蘭氏陰性菌的殺菌效果之機制探討

Action Mechanism of CX in Increasing the Bactericidal Effect by Antibiotics on Gram-negative Bacteria

指導教授 : 陳進庭

摘要


臨床上,目前普遍使用抗生素治療因革蘭氏陰性菌所引起的感染症,這樣的治療方法缺點在於抗生素的濫用帶來的篩選壓力,使得抗藥性細菌出現。革蘭氏陰性菌具有多重的抗藥性機制,一旦發現抗藥性菌株大多已是多重抗藥性菌株,造成後續治療上的困難。本實驗室先前研究發現,CX能有效加強光動力的殺菌效果,希望藉由CX的協助加強抗生素對革蘭氏陰性菌的殺菌效果,降低抗生素的使用量。 研究發現,CX和抗生素作用與抗生素單獨使用時相比較,發現能多降低7個log值生菌數而達全殺的效果,而且加入CX於不同抗生素的MIC濃度時,最終達到的殺菌效果顯著比使用MIC以上濃度的殺菌效果更好,因此CX可加強不同種類的抗生素對革蘭氏陰性菌之殺菌效果,同時亦能協助降低抗生素使用劑量;CX的加強殺菌效果也對抗藥性菌株有效,但CX無法加強EDTA在綠膿桿菌的殺菌效果。至於應用在綠膿桿菌的生物膜殺菌上,可能是受到胞外聚合物的阻礙使CX無法進入生物膜與細菌接觸,因此無法如同在懸浮培養上有增強殺菌的效果。未來實驗室計劃將朝向改良CX的性質與破壞生物膜表面的胞外聚合物,再觀察CX在抗生素對生物膜上的殺菌效果之影響

並列摘要


Antibiotics are the most popular antimicrobial agent used for the treatment of infection caused by Gram-negative bacteria. However, drug-resistance is a growing problem largely due to the widespread use of antibiotics in medicine. The opportunistic Pseudomonas aeruginosa (P. aeruginosa) is one of Gram-negative bacteria, which has been identified several drug-resistant strains in clinics. Therefore, it is necessary to develop an alternative antimicrobial technique which is effective in the treatment of multi-drug resistant bacteria infections. In the presence of compound X (CX), we have previously found that hematoporphyrin (Hp)-mediated photodynamic inactivation (PDI) could increase the bacterial killing against Gram-positive as well as Gram-negative bacteria. In this study, we further address whether CX can exert synergistic antimicrobial effect in antibiotics against Gram-negative bacteria. We found that CX can synergistically increase the antibiotics-mediated bactericidal effects. Under the MIC concentration, the bacterial effect of Polymyxin B 、 Colistin 、 Imipenem 、Gentamicin and Ciprofloxacin is around 2~3 log against P. aeruginosa in platonic culture; however, complete killing could be found in the presence of 0.25% CX. Similar results were also found in other Gram-negative bacterial, Acinetobacter baumannii。However, this synergistic effect of antibiotics and CX was not found in biofilm study, which might relate to the extracellular polymeric substances of biofilm.

參考文獻


53 蔣采昕。2007。細菌細胞壁組成對光動力治療抑制革蘭氏陽性菌與革蘭氏陰性菌效果之影響。國立台灣大學,微生物與生化學研究所碩士論文。
1 Mugabe, C., Halwani, M., Azghani, A. O., Lafrenie, R. M. and Omri, A. (2006) Mechanism of enhanced activity of liposome-entrapped aminoglycosides against resistant strains of Pseudomonas aeruginosa. Antimicrobial agents and chemotherapy. 50, 2016-2022
2 Tre-Hardy, M., Vanderbist, F., Traore, H. and Devleeschouwer, M. J. (2008) In vitro activity of antibiotic combinations against Pseudomonas aeruginosa biofilm and planktonic cultures. International journal of antimicrobial agents. 31, 329-336
3 Trafny, E. A. (1998) Susceptibility of adherent organisms from Pseudomonas aeruginosa and Staphylococcus aureus strains isolated from burn wounds to antimicrobial agents. International journal of antimicrobial agents. 10, 223-228
4 Donlan, R. M. (2002) Biofilms: microbial life on surfaces. Emerging infectious diseases. 8, 881-890

被引用紀錄


張博涵(2010)。以白色念珠菌為模式探討甲殼素增強光動力殺菌的效果〔碩士論文,國立臺灣大學〕。華藝線上圖書館。https://doi.org/10.6342/NTU.2010.00870

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