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抗菌肽对囊性纤维化患者分离病原体的抗菌和抗生物膜作用。

Antibacterial and anti-biofilm effects of cathelicidin peptides against pathogens isolated from cystic fibrosis patients.

机构信息

Department of Biomedical Sciences, G. d'Annunzio University of Chieti-Pescara, Via Vestini 31, 66100 Chieti, Italy.

出版信息

Peptides. 2011 Sep;32(9):1807-14. doi: 10.1016/j.peptides.2011.08.002. Epub 2011 Aug 7.

Abstract

Six different cathelicidin-derived peptides were compared to tobramycin for antibacterial and anti-biofilm effects against S. aureus, P. aeruginosa, and S. maltophilia strains isolated from cystic fibrosis patients. Overall, SMAP-29, BMAP-28, and BMAP-27 showed relevant antibacterial activity (MIC(50) 4-8μg/ml), and in some cases higher than tobramycin. In contrast, indolicidin, LL-37, and Bac7(1-35) showed no significant antimicrobial activity (MIC(50)>32μg/ml). Killing kinetics experiments showed that in contrast to tobramycin the active cathelicidin peptides exert a rapid bactericidal activity regardless of the species tested. All three peptides significantly reduced biofilm formation by S. maltophilia and P. aeruginosa strains at 1/2× MIC, although at a lower extent than tobramycin. In addition, BMAP-28, as well as tobramycin, was also active against S. aureus biofilm formation. Preformed biofilms were significantly affected by bactericidal SMAP-29, BMAP-27 and BMAP-28 concentrations, although at a lesser extent than tobramycin. Overall, our results indicate the potential of some cathelicidin-derived peptides for the development of novel therapeutic agents for cystic fibrosis lung disease.

摘要

六种不同的抗菌肽衍生肽与妥布霉素进行了比较,以评估它们对金黄色葡萄球菌、铜绿假单胞菌和粘质沙雷氏菌的抗菌和抗生物膜作用,这些菌株均从囊性纤维化患者中分离得到。总的来说,SMAP-29、BMAP-28 和 BMAP-27 表现出了相关的抗菌活性(MIC(50)为 4-8μg/ml),在某些情况下甚至高于妥布霉素。相比之下,Indolicidin、LL-37 和 Bac7(1-35)则没有明显的抗菌活性(MIC(50)>32μg/ml)。杀菌动力学实验表明,与妥布霉素不同,活性抗菌肽能够快速杀菌,而与测试的物种无关。这三种肽都能显著减少粘质沙雷氏菌和铜绿假单胞菌菌株的生物膜形成,在 1/2×MIC 时效果显著,尽管效果不及妥布霉素。此外,BMAP-28 与妥布霉素一样,也能有效抑制金黄色葡萄球菌生物膜的形成。杀菌浓度的 SMAP-29、BMAP-27 和 BMAP-28 显著影响了预先形成的生物膜,尽管效果不及妥布霉素。总的来说,我们的研究结果表明,一些抗菌肽衍生肽具有开发囊性纤维化肺部疾病新型治疗药物的潜力。

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