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Phage-host interactions during pseudolysogeny: Lessons from the Pid/dgo interaction
William Cenens1, Angella Makumi, Mehari Tesfazgi Mebrhatu
1Laboratory of Food Microbiology; Department of Microbial and Molecular Systems (M2S); Faculty of Bioscience Engineering; KU Leuven; Leuven, Belgium.
Abstract:
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.
Insights
Researchers discovered phage carrier cells in Salmonella Typhimurium, supporting pseudolysogeny. A novel phage protein (Pid) expressed in these cells impacts host metabolism.
Area of Science:
- Microbiology
- Bacteriology
- Virology
Background:
- Bacteriophage P22-Salmonella Typhimurium interactions are crucial for understanding bacterial genetics and evolution.
- Pseudolysogeny, a state where phage DNA persists without immediate lysis, has been historically challenging to study.
- Recent findings suggest a more intricate role for phages beyond simple infection or lysogeny.
Purpose of the Study:
- To provide molecular and genetic evidence for pseudolysogenic development in the Salmonella Typhimurium-phage P22 system.
- To investigate the role of a newly discovered P22 ORFan protein (Pid) in pseudolysogenic cells.
- To explore the impact of pseudolysogeny on both bacterial and phage biology.
Main Methods:
- Utilized the Salmonella Typhimurium-phage P22 model system.
- Employed molecular and genetic analyses to identify phage carrier cells.
- Observed the behavior of episomal phage elements during cell division.
- Analyzed the expression of the P22 ORFan protein (Pid) and its effect on the host dgo operon.
Main Results:
- Confirmed the existence of phage carrier cells harboring an episomal P22 element in Salmonella Typhimurium.
- Demonstrated asymmetric segregation of the episomal P22 element during bacterial cell division.
- Identified a novel P22 ORFan protein (Pid) specifically expressed in phage carrier cells.
- Showed that Pid can derepress a host metabolic operon (dgo), indicating phage influence on bacterial metabolism.
Conclusions:
- Pseudolysogenic development is a viable phenomenon in the Salmonella Typhimurium-phage P22 system.
- The P22 ORFan protein Pid plays a significant role in mediating phage-host interactions during pseudolysogeny.
- Pseudolysogeny has demonstrable effects on bacterial metabolism and potentially influences bacterial and phage evolution.
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