假溶解过程中噬菌体与宿主的相互作用:Pid/dgo 相互作用的启示。

Bacteriophage Pub Date : 2013-01-01 Epub Date: 2013-05-21 DOI:10.4161/bact.25029
William Cenens, Angella Makumi, Mehari Tesfazgi Mebrhatu, Rob Lavigne, Abram Aertsen
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引用次数: 0

摘要

尽管噬菌体感染的研究由来已久,并促进了我们目前对细菌遗传学、分子生物学、进化论和生态学的理解,但微生物学家似乎才刚刚开始探索噬菌体-宿主相互作用的复杂性。在 Cenens 等人最近发表的一篇手稿中,我们发现在鼠伤寒沙门氏菌-噬菌体 P22 模型系统中存在假溶解发育的分子和遗传学支持。更具体地说,我们观察到噬菌体载体细胞中存在一种外显的 P22 基因,这种基因在随后的分裂中不对称地分离。此外,一种新发现的 P22 ORFan 蛋白(Pid)能够解除对宿主代谢操作子(dgo)的抑制,并在这些噬菌体载体细胞中特异性表达。在本增编中,我们将进一步阐述假溶质形成及其对细菌和噬菌体生物学的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Phage-host interactions during pseudolysogeny: Lessons from the Pid/dgo interaction.

Although the study of phage infection has a long history and catalyzed much of our current understanding in bacterial genetics, molecular biology, evolution and ecology, it seems that microbiologists have only just begun to explore the intricacy of phage-host interactions. In a recent manuscript by Cenens et al. we found molecular and genetic support for pseudolysogenic development in the Salmonella Typhimurium-phage P22 model system. More specifically, we observed the existence of phage carrier cells harboring an episomal P22 element that segregated asymmetrically upon subsequent divisions. Moreover, a newly discovered P22 ORFan protein (Pid) able to derepress a metabolic operon of the host (dgo) proved to be specifically expressed in these phage carrier cells. In this addendum we expand on our view regarding pseudolysogeny and its effects on bacterial and phage biology.

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