Department of Microbiology and Immunology, University of Otago, PO Box 56, Dunedin 9054, New Zealand.
Department of Microbiology and Immunology, University of Otago, PO Box 56, Dunedin 9054, New Zealand; Bio-Protection Research Centre, University of Otago, PO Box 56, Dunedin 9054, New Zealand.
Curr Opin Biotechnol. 2021 Apr;68:30-36. doi: 10.1016/j.copbio.2020.09.008. Epub 2020 Oct 24.
The rise of antibiotic-resistant bacteria has led to renewed interest in the use of their natural enemies, phages, for the prevention and treatment of infections. However, phage therapy requires detailed knowledge of the interactions between these entities. Bacteria defend themselves against phage predation with a large repertoire of defences. Among these, CRISPR-Cas systems stand out due to their adaptive character, mechanistic complexity and diversity, and present a significant hurdle for phage infection. Here, we provide an overview of how phages can circumvent CRISPR-Cas defence, ranging from target sequence mutations and DNA modifications to anti-CRISPR proteins and nucleus-like protective structures. An in-depth understanding of these phage evasion strategies is crucial for the successful development of phage therapy applications.
抗生素耐药菌的出现重新引起了人们对利用其天敌噬菌体预防和治疗感染的兴趣。然而,噬菌体疗法需要详细了解这些实体之间的相互作用。细菌通过多种防御机制来保护自己免受噬菌体的捕食。其中,CRISPR-Cas 系统因其适应性、机制复杂性和多样性而脱颖而出,是噬菌体感染的一个重大障碍。在这里,我们概述了噬菌体如何规避 CRISPR-Cas 防御,包括靶序列突变和 DNA 修饰、抗 CRISPR 蛋白和类似核的保护结构。深入了解这些噬菌体逃避策略对于成功开发噬菌体治疗应用至关重要。