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抗葡萄球菌内溶素LysRODI在pH敏感脂质体中的包封

Encapsulation of the Antistaphylococcal Endolysin LysRODI in pH-Sensitive Liposomes.

作者信息

Portilla Silvia, Fernández Lucía, Gutiérrez Diana, Rodríguez Ana, García Pilar

机构信息

Instituto de Productos Lácteos de Asturias (IPLA-CSIC), Paseo Río Linares s/n, Villaviciosa, 33300 Asturias, Spain.

DairySafe Group, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Oviedo, 33011 Asturias, Spain.

出版信息

Antibiotics (Basel). 2020 May 9;9(5):242. doi: 10.3390/antibiotics9050242.

Abstract

Phage lysins are promising new therapeutics against multidrug-resistant bacteria. These so-called enzybiotics offer, amongst their most notable advantages, high target specificity and low resistance development. Moreover, there are numerous recent and ongoing studies aimed at demonstrating the efficacy and safety of endolysins in animal models or even in clinical trials. Nonetheless, as is the case for other antimicrobials, it is important to assess potential strategies that may broaden their potential applications or improve their stability. Encapsulation, for instance, has given very good results for some antibiotics. This study sought to evaluate the feasibility of encapsulating an endolysin against the opportunistic human pathogen , one of the most problematic bacteria in the context of the current antibiotic resistance crisis. Endolysin LysRODI has antimicrobial activity against many strains from different sources, including methicillin-resistant (MRSA) isolates. Here, this protein was encapsulated in pH-sensitive liposomes with an efficacy of approximately 47%, retaining its activity after being released from the nanocapsules. Additionally, the encapsulated endolysin effectively reduced cell counts by > 2log units in both planktonic cultures and biofilms upon incubation at pH 5. These results demonstrate the viability of LysRODI encapsulation in liposomes for its targeted delivery under mild acidic conditions.

摘要

噬菌体裂解素是对抗多重耐药细菌的有前景的新型治疗剂。这些所谓的酶抗生素具有诸多显著优势,其中包括高靶向特异性和低耐药性发展。此外,近期有大量研究正在进行,旨在证明内溶素在动物模型甚至临床试验中的疗效和安全性。尽管如此,与其他抗菌药物一样,评估可能拓宽其潜在应用或提高其稳定性的潜在策略很重要。例如,包封对某些抗生素已取得了很好的效果。本研究旨在评估包封一种针对人类机会致病菌的内溶素的可行性,该菌是当前抗生素耐药危机背景下最具问题的细菌之一。内溶素LysRODI对来自不同来源的许多菌株具有抗菌活性,包括耐甲氧西林金黄色葡萄球菌(MRSA)分离株。在此,该蛋白被包封在pH敏感脂质体中,包封效率约为47%,从纳米胶囊释放后仍保留其活性。此外,在pH 5孵育时,包封的内溶素在浮游培养物和生物膜中均有效降低了金黄色葡萄球菌细胞计数>2个对数单位。这些结果证明了将LysRODI包封在脂质体中以便在温和酸性条件下进行靶向递送的可行性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abf1/7277728/ee14be71ecc9/antibiotics-09-00242-g001.jpg

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