Rubino Ilaria, Guerrero-Bustamante Carlos A, Harrison Melissa, Co Sheila, Tetreau Isobel, Ordoubadi Mani, Larsen Sasha E, Coler Rhea N, Vehring Reinhard, Hatfull Graham F, Sauvageau Dominic
Department of Chemical and Materials Engineering, University of Alberta, Edmonton, Alberta, Canada.
Département de Génie Chimique et de Génie Biotechnologique, Université de Sherbrooke, Sherbrooke, Québec, Canada.
bioRxiv. 2024 Oct 29:2024.10.23.619922. doi: 10.1101/2024.10.23.619922.
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 -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 () 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, alone and in cocktail formulations, under different host growth conditions, and serve as a basis for the development of phage products targeting mycobacteria biofilms.
仅在2022年,全球结核病疫情就影响了1000万人,并导致130万人死亡。耐多药结核病在不到60%的病例中通过长期、昂贵且激进的治疗得以成功治愈。分枝杆菌噬菌体是一种能够感染诸如导致结核病的细菌物种的病毒,它有可能重新定义结核病的预防和治疗方法。然而,基于噬菌体的产品的开发需要评估众多参数,包括毒性和吸附作用,以确保其性能和质量。在这项研究中,我们对三种不同的分枝杆菌噬菌体(Fionnbharth、Muddy和D29)单独以及作为混合物,在浮游和早期生物膜生长条件下,针对一种结核病模型宿主()的毒性进行了表征。噬菌体D29以及含有D29的混合物在所有条件下都具有最高的毒性。有趣的是,噬菌体Fionnbharth和Muddy及其组合对早期生物膜的毒性比对浮游表型的毒性更高。吸附试验表明,所有三种噬菌体在早期生物膜表型上的吸附效率都低于在浮游表型上的吸附效率,这表明前者的受体可用性较低。鉴于尽管吸附效率较低,但噬菌体和噬菌体混合物对早期生物膜的毒性要么未变,要么更高,这种表型必定具有有利于感染过程其他步骤的特性。这些结果让我们了解了分枝杆菌噬菌体单独以及以混合物形式在不同宿主生长条件下的感染动态,并为开发针对分枝杆菌生物膜的噬菌体产品奠定了基础。