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噬菌体在其生命周期中作为固有部分来避免同源免疫系统的自身免疫。

Bacteriophages avoid autoimmunity from cognate immune systems as an intrinsic part of their life cycles.

机构信息

Centre for Bacterial Resistance Biology, Imperial College London, London, UK.

School of Health Sciences, Universidad CEU Cardenal Herrera, CEU Universities, Alfara del Patriarca, Spain.

出版信息

Nat Microbiol. 2024 May;9(5):1312-1324. doi: 10.1038/s41564-024-01661-6. Epub 2024 Apr 2.

Abstract

Dormant prophages protect lysogenic cells by expressing diverse immune systems, which must avoid targeting their cognate prophages upon activation. Here we report that multiple Staphylococcus aureus prophages encode Tha (tail-activated, HEPN (higher eukaryotes and prokaryotes nucleotide-binding) domain-containing anti-phage system), a defence system activated by structural tail proteins of incoming phages. We demonstrate the function of two Tha systems, Tha-1 and Tha-2, activated by distinct tail proteins. Interestingly, Tha systems can also block reproduction of the induced tha-positive prophages. To prevent autoimmunity after prophage induction, these systems are inhibited by the product of a small overlapping antisense gene previously believed to encode an excisionase. This genetic organization, conserved in S. aureus prophages, allows Tha systems to protect prophages and their bacterial hosts against phage predation and to be turned off during prophage induction, balancing immunity and autoimmunity. Our results show that the fine regulation of these processes is essential for the correct development of prophages' life cycle.

摘要

潜伏噬菌体通过表达多样化的免疫系统来保护溶原细胞,而这些免疫系统在被激活时必须避免针对其同源噬菌体。在这里,我们报告称,多个金黄色葡萄球菌噬菌体编码 Tha(尾部激活、含有 HEPN(高等真核生物和原核生物核苷酸结合)结构域的抗噬菌体系统),这是一种由进入噬菌体的结构尾部蛋白激活的防御系统。我们证明了两种 Tha 系统 Tha-1 和 Tha-2 的功能,它们分别被不同的尾部蛋白激活。有趣的是,Tha 系统还可以阻止诱导的 tha 阳性噬菌体的繁殖。为了防止噬菌体诱导后发生自身免疫,以前被认为编码切除酶的小重叠反义基因的产物抑制这些系统。这种在金黄色葡萄球菌噬菌体中保守的遗传组织允许 Tha 系统保护噬菌体及其细菌宿主免受噬菌体捕食,并在噬菌体诱导期间关闭,从而平衡免疫和自身免疫。我们的研究结果表明,这些过程的精细调控对于噬菌体生命周期的正确发展至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b9d/11087260/325fafd50c1d/41564_2024_1661_Fig1_HTML.jpg

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