Núñez-Sánchez María A, Colom Joan, Walsh Lauren, Buttimer Colin, Bolocan Andrei Sorin, Pang Rory, Gahan Cormac G M, Hill Colin
APC Microbiome Ireland, Bioscience institute, University College Cork, Cork T12 YT20 , Ireland.
School of Microbiology, University College Cork, Cork, T12 YN60, Ireland.
Microorganisms. 2020 Sep 7;8(9):1374. doi: 10.3390/microorganisms8091374.
An intestinal epithelium model able to produce mucus was developed to provide an environment suitable for testing the therapeutic activity of gut bacteriophages. We show that adheres more effectively in the presence of mucus, can invade the intestinal epithelia and is able to translocate after damaging tight junctions. Furthermore, phage vB_EfaM_A2 (a member of that possesses virion associated immunoglobin domains) was found to translocate through the epithelium in the presence and absence of its host bacteria. Phage A2 protected eukaryotic cells by reducing mortality and maintaining the structure of the cell layer structure. We suggest the mammalian cell model utilized within this study as an adaptable in vitro model that can be employed to enable a better understanding of phage-bacteria interactions and the protective impact of phage therapy relating to the intestinal epithelium.
开发了一种能够产生黏液的肠上皮模型,以提供适合测试肠道噬菌体治疗活性的环境。我们发现,[噬菌体名称]在黏液存在的情况下黏附更有效,能够侵入肠上皮细胞,并在破坏紧密连接后发生移位。此外,发现噬菌体vB_EfaM_A2([噬菌体家族名称]的成员,具有与病毒体相关的免疫球蛋白结构域)在有或无宿主细菌存在的情况下都能通过上皮细胞移位。噬菌体A2通过降低死亡率和维持细胞层结构来保护真核细胞。我们建议将本研究中使用的哺乳动物细胞模型作为一种适应性强的体外模型,可用于更好地理解噬菌体 - 细菌相互作用以及噬菌体疗法对肠上皮的保护作用。