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富含脯氨酸的抗菌肽B7-005:细菌耐药性低,对人体细胞安全,在斑马鱼胚胎菌血症模型中有效。

The proline-rich antimicrobial peptide B7-005: low bacterial resistance, safe for human cells and effective in zebrafish embryo bacteraemia model.

作者信息

Di Stasi Adriana, Bozzer Sara, Pacor Sabrina, de Pascale Luigi, Morici Martino, Favero Lara, Spazzapan Mariagiulia, Pegoraro Silvia, Bulla Roberta, Wilson Daniel N, Macor Paolo, Scocchi Marco, Mardirossian Mario

机构信息

Department of Life Sciences, University of Trieste, 34127 Trieste, Italy.

Institute for Biochemistry and Molecular Biology, University of Hamburg, 20146 Hamburg, Germany.

出版信息

Open Biol. 2024 Dec;14(12):240286. doi: 10.1098/rsob.240286. Epub 2024 Dec 4.

Abstract

Proline-rich antimicrobial peptides (PrAMPs) have gained attention due to their antimicrobial properties and low cytotoxicity. B7-005, a small optimized PrAMP, exhibits a broader spectrum of activity than native PrAMPs, due to an antimicrobial mechanism based on inhibiting prokaryotic protein synthesis and destabilizing bacterial membranes. However, the toxicity and the efficacy of B7-005 remain poorly understood, so and microbiology and toxicology experiments were used to assess its suitability as an anti-infective agent. The incidence of resistance towards B7-005 by was lower than for other PrAMPs and antibiotics; moreover, it maintained antimicrobial activity in the presence of human serum. B7-005 exerted its antimicrobial effect at a much lower concentration than those causing harmful effects on four different cell types, such as membrane permeabilization or non-lytic depolarization of mitochondria. The latter effect may be related to the inhibition of eukaryotic protein synthesis by B7-005 observed . In a zebrafish embryo model, B7-005 was well tolerated and reduced mortality from pre-existing bacteraemia. Overall, B7-005 was safe for human cells and effective against systemic infection , making it a promising lead for developing new antibiotics.

摘要

富含脯氨酸的抗菌肽(PrAMPs)因其抗菌特性和低细胞毒性而受到关注。B7 - 005是一种经过优化的小PrAMP,由于其基于抑制原核生物蛋白质合成和破坏细菌膜的抗菌机制,其活性谱比天然PrAMPs更广泛。然而,B7 - 005的毒性和功效仍知之甚少,因此通过微生物学和毒理学实验来评估其作为抗感染剂的适用性。对B7 - 005产生耐药性的发生率低于其他PrAMPs和抗生素;此外,它在人血清存在的情况下仍保持抗菌活性。B7 - 005发挥抗菌作用的浓度远低于对四种不同细胞类型产生有害影响的浓度,如膜通透性改变或线粒体非裂解性去极化。后一种效应可能与观察到的B7 - 005对真核生物蛋白质合成的抑制有关。在斑马鱼胚胎模型中,B7 - 005耐受性良好,并降低了先前存在的菌血症导致的死亡率。总体而言,B7 - 005对人类细胞安全且对全身感染有效,使其成为开发新型抗生素的有前途的先导物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2b3/11614538/133583bcf93d/rsob.240286.f001.jpg

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