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Phage–host interactions during pseudolysogeny

机译:在pseudolysogeny Phage-host交互

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摘要

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 phagecarrier cells. In this addendum we expand on our view regarding pseudolysogeny and its effects on bacterial and phage biology.
机译:虽然噬菌体感染的研究有很长的我们当前的历史和催化理解细菌遗传学,分子生物学、进化和生态学,似乎微生物学家才刚刚开始探索phage-host错综复杂的相互作用。最近的手稿Cenens等人发现分子和遗传对pseudolysogenic的支持沙门氏菌Typhimurium-phage发展第22位模型系统。窝藏一个噬菌体载体细胞的存在游离第22位元素隔离不对称在随后的分歧。此外,新发现的第22位ORFan蛋白质(Pid)能够去抑制代谢的操纵子主机(dgo)被证明是特别表达这些phagecarrier细胞。关于pseudolysogeny和扩展我们的视野对细菌和噬菌体生物学的影响。

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