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与亲本肽相比,蛙皮抗菌肽天蚕素1Tb的类似物表现出更广泛的活性谱和更强的抗生物膜潜力。

Analogs of the Frog-skin Antimicrobial Peptide Temporin 1Tb Exhibit a Wider Spectrum of Activity and a Stronger Antibiofilm Potential as Compared to the Parental Peptide.

作者信息

Grassi Lucia, Maisetta Giuseppantonio, Maccari Giuseppe, Esin Semih, Batoni Giovanna

机构信息

Department of Translational Research and new Technologies in Medicine and Surgery, University of PisaPisa, Italy.

Center for Nanotechnology Innovation @NEST, Italian Institute of TechnologyPisa, Italy.

出版信息

Front Chem. 2017 Apr 11;5:24. doi: 10.3389/fchem.2017.00024. eCollection 2017.

Abstract

The frog skin-derived peptide Temporin 1Tb (TB) has gained increasing attention as novel antimicrobial agent for the treatment of antibiotic-resistant and/or biofilm-mediated infections. Nevertheless, such a peptide possesses a preferential spectrum of action against Gram-positive bacteria. In order to improve the therapeutic potential of TB, the present study evaluated the antibacterial and antibiofilm activities of two TB analogs against medically relevant bacterial species. Of the two analogs, TB_KKG6A has been previously described in the literature, while TB_L1FK is a new analog designed by us through statistical-based computational strategies. Both TB analogs displayed a faster and stronger bactericidal activity than the parental peptide, especially against Gram-negative bacteria in planktonic form. Differently from the parental peptide, TB_KKG6A and TB_L1FK were able to inhibit the formation of biofilms by more than 50% at 12 μM, while only TB_KKG6A prevented the formation of biofilms at 24 μM. A marked antibiofilm activity against preformed biofilms of both bacterial species was observed for the two TB analogs when used in combination with EDTA. Analysis of synergism at the cellular level suggested that the antibiofilm activity exerted by the peptide-EDTA combinations against mature biofilms might be due mainly to a disaggregating effect on the extracellular matrix in the case of , and to a direct activity on biofilm-embedded cells in the case of . Both analogs displayed a low hemolytic effect at the active concentrations and, overall, TB_L1FK resulted less cytotoxic toward mammalian cells. Collectively, the results obtained demonstrated that subtle changes in the primary sequence of TB may provide TB analogs that, used alone or in combination with adjuvant molecules such as EDTA, exhibit promising features against both planktonic and biofilm cells of medically relevant bacteria.

摘要

源自蛙皮的肽Temporin 1Tb(TB)作为一种新型抗菌剂,在治疗抗生素耐药和/或生物膜介导的感染方面越来越受到关注。然而,这种肽对革兰氏阳性菌具有优先作用谱。为了提高TB的治疗潜力,本研究评估了两种TB类似物对医学相关细菌物种的抗菌和抗生物膜活性。在这两种类似物中,TB_KKG6A先前已在文献中描述,而TB_L1FK是我们通过基于统计的计算策略设计的新类似物。两种TB类似物均表现出比亲本肽更快、更强的杀菌活性,尤其是对浮游形式的革兰氏阴性菌。与亲本肽不同,TB_KKG6A和TB_L1FK在12 μM时能够抑制超过50%的生物膜形成,而只有TB_KKG6A在24 μM时能阻止生物膜形成。当与EDTA联合使用时,两种TB类似物对两种细菌物种预先形成的生物膜均表现出显著的抗生物膜活性。细胞水平的协同分析表明,肽 - EDTA组合对成熟生物膜发挥的抗生物膜活性,在[具体情况1]下可能主要归因于对细胞外基质的解聚作用,在[具体情况2]下则归因于对生物膜包埋细胞的直接作用。两种类似物在活性浓度下均表现出低溶血作用,总体而言,TB_L1FK对哺乳动物细胞的细胞毒性较小。总的来说,所获得的结果表明,TB一级序列的细微变化可能产生TB类似物,这些类似物单独使用或与EDTA等佐剂分子联合使用时,对医学相关细菌的浮游和生物膜细胞均表现出有前景的特性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4700/5387044/52e3106b3cfa/fchem-05-00024-g0001.jpg

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