Enhancement of the efficacy of erythromycin in multiple antibiotic-resistant gram-negative bacterial pathogens

被引:40
作者
Saha, S.
Savage, P. B. [2 ]
Bal, M. [1 ]
机构
[1] Univ Calcutta, Univ Coll Sci & Technol, Dept Physiol, Microbiol Sect, Kolkata 700009, W Bengal, India
[2] Brigham Young Univ, Dept Chem & Biochem, Provo, UT 84602 USA
关键词
amphiphilic Ceragenin CSA-13; erythromycin resistance; hydrophobic antibiotic; multiple antibiotic resistance; outer membrane permeabilizer;
D O I
10.1111/j.1365-2672.2008.03820.x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aims: To improve the efficacy of erythromycin, a hydrophobic antibiotic, against multiple antibiotic-resistant gram-negative bacterial pathogens by enhancing their outer membrane permeability. Methods and Results: Fifty-one nonrepeat gram-negative bacterial pathogens of various genera, resistant to multiple antibiotics, including erythromycin, were selected by disc agar diffusion tests. The amphiphilic cationic steroid antibiotic, Ceragenin CSA-13, a potent permeabilizer of bacterial outer membranes, reduced the minimum inhibitory concentration of erythromycin in 92% of the bacterial pathogens selected for the test, when supplemented with erythromycin. A synergistic effect of Ceragenin CSA-13 and erythromycin in combination was also observed. Spectrofluorimetric study confirmed that Ceragenin CSA-13 acts by depolarizing the bacterial outer membrane. The toxicity of Ceragenin CSA-13 was evaluated to be insignificant by measuring 'median lethal dose' (LD50) on mouse model. Conclusions: Ceragenin CSA-13 may be useful as an agent to make erythromycin effective against infections caused by multiple antibiotic resistant gram-negative bacteria. Significance and Impact of the Study: The outcome of the study suggests erythromycin-Ceragenin combination as a new approach to overcome the problem associated with the rapid emergence of multi-drug-resistant pathogens. The insignificant toxicity of Ceragenin CSA-13, as found, supports the possibility of the application of this compound for human therapeutics.
引用
收藏
页码:822 / 828
页数:7
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