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抗菌光动力疗法通过肽 aurein 1.2 得到增强。

Antimicrobial Photodynamic therapy enhanced by the peptide aurein 1.2.

机构信息

Universidade Estadual Paulista (Unesp), Faculdade de Ciências Farmacêuticas, Araraquara, SP, Rodovia Araraquara-Jaú, km 1, Campus Ville, CEP, 14800-903, Brazil.

Universidade Federal de Goiás, Instituto de Ciências Biológicas, Departamento de Bioquímica e Biologia Molecular, Campus II Samambaia, 74690-900, Goiânia, GO, Brazil.

出版信息

Sci Rep. 2018 Mar 9;8(1):4212. doi: 10.1038/s41598-018-22687-x.

DOI:10.1038/s41598-018-22687-x
PMID:29523862
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5844988/
Abstract

In the past few years, the World Health Organization has been warning that the post-antibiotic era is an increasingly real threat. The rising and disseminated resistance to antibiotics made mandatory the search for new drugs and/or alternative therapies that are able to eliminate resistant microorganisms and impair the development of new forms of resistance. In this context, antimicrobial photodynamic therapy (aPDT) and helical cationic antimicrobial peptides (AMP) are highlighted for the treatment of localized infections. This study aimed to combine the AMP aurein 1.2 to aPDT using Enterococcus faecalis as a model strain. Our results demonstrate that the combination of aPDT with aurein 1.2 proved to be a feasible alternative capable of completely eliminating E. faecalis employing low concentrations of both PS and AMP, in comparison with the individual therapies. Aurein 1.2 is capable of enhancing the aPDT activity whenever mediated by methylene blue or chlorin-e6, but not by curcumin, revealing a PS-dependent mechanism. The combined treatment was also effective against different strains; noteworthy, it completely eliminated a vancomycin-resistant strain of Enterococcus faecium. Our results suggest that this combined protocol must be exploited for clinical applications in localized infections as an alternative to antibiotics.

摘要

在过去的几年里,世界卫生组织一直警告说,后抗生素时代是一个日益严重的现实威胁。抗生素耐药性的不断上升和传播,使得寻找新的药物和/或替代疗法变得势在必行,这些疗法能够消除耐药微生物,并防止新形式的耐药性产生。在这种情况下,光动力抗菌疗法(aPDT)和螺旋阳离子抗菌肽(AMP)因其能够治疗局部感染而备受关注。本研究旨在将 AMP aurein 1.2 与 aPDT 结合,使用粪肠球菌作为模型菌株。我们的研究结果表明,与单独使用两种 PS 和 AMP 相比,aPDT 联合 aurein 1.2 可以作为一种可行的替代方案,能够完全消除粪肠球菌,而且只需使用低浓度的 PS 和 AMP。aurein 1.2 能够增强由亚甲蓝或氯己定介导的 aPDT 活性,但不能增强由姜黄素介导的 aPDT 活性,这表明其作用机制与 PS 有关。联合治疗对不同的菌株也有效;值得注意的是,它完全消除了一株耐万古霉素的屎肠球菌。我们的研究结果表明,这种联合方案可以作为抗生素的替代方案,用于局部感染的临床应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8bc/5844988/de035d057c13/41598_2018_22687_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8bc/5844988/e3aafaa17d8d/41598_2018_22687_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8bc/5844988/204d7a144f71/41598_2018_22687_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8bc/5844988/a3b91f316c85/41598_2018_22687_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8bc/5844988/e34e52367a78/41598_2018_22687_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8bc/5844988/c0bff30b3f5e/41598_2018_22687_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8bc/5844988/6c0fe7a81125/41598_2018_22687_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8bc/5844988/ffbb2b5e5218/41598_2018_22687_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8bc/5844988/2b0c9348ecb2/41598_2018_22687_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8bc/5844988/de035d057c13/41598_2018_22687_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8bc/5844988/e3aafaa17d8d/41598_2018_22687_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8bc/5844988/204d7a144f71/41598_2018_22687_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8bc/5844988/a3b91f316c85/41598_2018_22687_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8bc/5844988/e34e52367a78/41598_2018_22687_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8bc/5844988/c0bff30b3f5e/41598_2018_22687_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8bc/5844988/6c0fe7a81125/41598_2018_22687_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8bc/5844988/ffbb2b5e5218/41598_2018_22687_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8bc/5844988/2b0c9348ecb2/41598_2018_22687_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8bc/5844988/de035d057c13/41598_2018_22687_Fig9_HTML.jpg

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