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基因内抗菌肽 Hs02 抑制 和 的单种和两种生物膜的增殖:减轻生物膜相关感染的有前途的药物。

Intragenic Antimicrobial Peptide Hs02 Hampers the Proliferation of Single- and Dual-Species Biofilms of and : A Promising Agent for Mitigation of Biofilm-Associated Infections.

机构信息

LAQV/Requimte, Departamento de Química e Bioquímica, Faculdade de Ciências da, Universidade do Porto, 4050-313 Porto, Portugal.

Laboratório de Síntese e Análise de Biomoléculas, Instituto de Química, Universidade de Brasília, UnB, Brasília DF 70910-900, Brasil.

出版信息

Int J Mol Sci. 2019 Jul 23;20(14):3604. doi: 10.3390/ijms20143604.

Abstract

and are two major pathogens involved in a large variety of infections. Their co-occurrence in the same site of infection has been frequently reported and is linked to enhanced virulence and difficulty of treatment. Herein, the antimicrobial and antibiofilm activities of an intragenic antimicrobial peptide (IAP), named Hs02, which was uncovered from the human unconventional myosin 1H protein, were investigated against several and strains, including multidrug-resistant (MDR) isolates. The antibiofilm activity was evaluated on single- and dual-species biofilms of and . Moreover, the effect of peptide Hs02 on the membrane fluidity of the strains was assessed through Laurdan generalized polarization (GP). Minimum inhibitory concentration (MIC) values of peptide Hs02 ranged from 2 to 16 μg/mL against all strains and MDR isolates. Though Hs02 was not able to hamper biofilm formation by some strains at sub-MIC values, it clearly affected 24 h preformed biofilms, especially by reducing the viability of the bacterial cells within the single- and dual-species biofilms, as shown by confocal laser scanning microscopy (CLSM) and atomic force microscopy (AFM) images. Laurdan GP values showed that Hs02 induces membrane rigidification in both and . Peptide Hs02 can potentially be a lead for further improvement as an antibiofilm agent.

摘要

和 是两种主要的病原体,涉及多种感染。它们在同一感染部位的同时存在已被频繁报道,并与增强的毒力和治疗难度有关。在此,研究了一种从人类非传统肌球蛋白 1H 蛋白中发现的基因内抗菌肽 (IAP) Hs02 对几种 和 菌株的抗菌和抗生物膜活性,包括多药耐药 (MDR) 分离株。在 和 的单种和双种生物膜上评估了抗生物膜活性。此外,通过 Laurdan 广义偏振 (GP) 评估了肽 Hs02 对菌株膜流动性的影响。肽 Hs02 对所有菌株和 MDR 分离株的最小抑菌浓度 (MIC) 值范围为 2 至 16 μg/mL。尽管 Hs02 不能在亚 MIC 值下阻止某些菌株的生物膜形成,但它显然会影响 24 小时形成的生物膜,尤其是通过减少单种和双种生物膜中细菌细胞的活力,如共聚焦激光扫描显微镜 (CLSM) 和原子力显微镜 (AFM) 图像所示。Laurdan GP 值表明 Hs02 诱导 和 中的膜刚性化。肽 Hs02 可能是进一步作为抗生物膜剂改进的潜在先导。

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