Comparative study on the virulence of mycobacteriophages.

IF 3.8 2区 医学 Q2 VIROLOGY
Journal of Virology Pub Date : 2025-06-17 Epub Date: 2025-05-21 DOI:10.1128/jvi.01920-24
Ilaria Rubino, Carlos A Guerrero-Bustamante, Melissa Harrison, Sheila Co, Isobel Tetreau, Mani Ordoubadi, Sasha E Larsen, Rhea N Coler, Reinhard Vehring, Graham F Hatfull, Dominic Sauvageau
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引用次数: 0

Abstract

The global tuberculosis (TB) epidemic affected 10 million people and caused 1.3 million deaths in 2022 alone. Multidrug-resistant TB is successfully treated in less than 60% of cases by long, expensive, and aggressive treatments. Mycobacteriophages, viruses that can infect bacteria such as Mycobacterium tuberculosis-the species responsible for TB-have the potential to redefine TB prevention and treatments. However, the development of phage-based products necessitates the assessment of numerous parameters, including virulence and adsorption, to ensure their performance and quality. In this work, we characterized the virulence of three different mycobacteriophages (Fionnbharth, Muddy, and D29), alone and as cocktails, against a TB model host (Mycobacterium smegmatis) under planktonic and early-stage biofilm growth conditions. Phage D29 and cocktails containing D29 had the highest virulence under all conditions. Interestingly, phages Fionnbharth and Muddy and their combination showed higher virulence against early-stage biofilm than against the planktonic phenotype. Adsorption assays indicated that all three phages had lower adsorption efficiencies on the early-stage biofilm phenotype than on the planktonic one, suggesting a reduced availability of receptors in the former. Given that, despite these lower adsorption efficiencies, the virulence of the phages and phage cocktails was either unchanged or higher against the early-stage biofilm, this phenotype must display properties that are favorable to other steps of the infection process. These results inform us on the dynamics of mycobacteriophage infections, both alone and in cocktail formulations, under different host growth conditions, serving as a basis for the development of phage products targeting mycobacteria biofilms.

Importance: This study provides a systematic investigation of the virulence of three mycobacteriophages, Fionnbharth, Muddy, and D29, and their combinations as cocktails against Mycobacterium smegmatis. We also included considerations on the hydrodynamic conditions (shaking and not shaking) and host phenotype (planktonic and early-onset biofilm cultures) during the infection process and adsorption of the phage to the host. We showed that virulence was strongly affected by phenotype and that higher virulence shown against the early-onset biofilm phenotype was not linked to faster adsorption to the host. We also showed that phage D29 and cocktails containing this phage had the highest virulence. These results are important as they provide a framework for a better evaluation and development of phage-based treatment against mycobacterial infections.

分枝噬菌体毒力的比较研究。
仅在2022年,全球结核病流行就影响了1000万人,造成130万人死亡。通过长期、昂贵和积极的治疗,只有不到60%的耐多药结核病病例得到成功治疗。分枝杆菌噬菌体是一种能够感染结核分枝杆菌等细菌的病毒——结核分枝杆菌是导致结核病的物种——它有可能重新定义结核病的预防和治疗。然而,基于噬菌体的产品的开发需要评估许多参数,包括毒力和吸附,以确保其性能和质量。在这项工作中,我们描述了三种不同的分枝噬菌体(fionnharth、Muddy和D29)在浮游和早期生物膜生长条件下单独和混合对结核模型宿主(污垢分枝杆菌)的毒力。在所有条件下,噬菌体D29和含有D29的鸡尾酒的毒力最高。有趣的是,噬菌体fionnharth和Muddy及其组合对早期生物膜的毒力高于对浮游表型的毒力。吸附实验表明,这三种噬菌体在早期生物膜表型上的吸附效率都低于浮游生物表型,这表明前者的受体可用性降低。考虑到,尽管这些较低的吸附效率,噬菌体和噬菌体鸡尾酒对早期生物膜的毒力要么不变,要么更高,这种表型必须显示有利于感染过程其他步骤的特性。这些结果告诉我们,在不同的宿主生长条件下,分枝杆菌噬菌体感染的动态,无论是单独的还是鸡尾酒制剂,都可以作为开发针对分枝杆菌生物膜的噬菌体产品的基础。重要性:本研究系统地研究了fionnharth、Muddy和D29这三种噬菌体对耻垢分枝杆菌的毒力,以及它们作为鸡尾酒的组合。在感染过程和噬菌体对宿主的吸附过程中,我们还考虑了流体动力学条件(摇动和不摇动)和宿主表型(浮游和早发生物膜培养)。我们发现,毒力受到表型的强烈影响,而对早发性生物膜表型的高毒力与宿主的更快吸附无关。我们还发现噬菌体D29和含有该噬菌体的鸡尾酒具有最高的毒力。这些结果很重要,因为它们为更好地评估和开发基于噬菌体的分枝杆菌感染治疗提供了一个框架。
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来源期刊
Journal of Virology
Journal of Virology 医学-病毒学
CiteScore
10.10
自引率
7.40%
发文量
906
审稿时长
1 months
期刊介绍: Journal of Virology (JVI) explores the nature of the viruses of animals, archaea, bacteria, fungi, plants, and protozoa. We welcome papers on virion structure and assembly, viral genome replication and regulation of gene expression, genetic diversity and evolution, virus-cell interactions, cellular responses to infection, transformation and oncogenesis, gene delivery, viral pathogenesis and immunity, and vaccines and antiviral agents.
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