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Molecular piracy in deep-sea hydrothermal vent: phage-plasmid interactions revealed by phage-FISH in Marinitoga
Min Jin1,2,3, Ouafae Rouxel1,3, Nadège Quintin1,3
1Univ Brest, Ifremer, BEEP, Plouzané, France.
Abstract:
Prokaryotes and mobile genetic elements (MGEs, such as viruses and plasmids) interact extensively, leading to horizontal gene transfer (HGT) and consequent microbial evolution and diversity. However, our knowledge of the interactions between MGEs in deep-sea hydrothermal ecosystems is limited. In this study, we adapted a phage-fluorescence in situ hybridization (phage-FISH) approach to visualize and quantify the dynamics of phage-plasmid interactions in an anaerobic, thermophilic deep-sea bacterium, Marinitoga piezophila. Notably, our results revealed that plasmid signals were detected in viral particles released from lysed cells, indicating that mitomycin C not only induced plasmid replication but also its packaging into phage particles. Further analysis of the DNA content in purified virions showed that the phage capsids incorporated plasmid DNA even without induction, and the majority of capsids (up to 70%) preferentially packaged plasmid DNA rather than viral DNA after induction. Therefore, this study provided direct evidence of molecular piracy in the deep-sea hydrothermal ecosystem, highlighting the important roles of selfish MGEs in virus-host interactions and HGT in extreme marine environments.
Importance:
Deep-sea hydrothermal vents are hotspots for microbes. Several studies revealed that virus-mediated horizontal gene transfer (HGT) in deep-sea hydrothermal vent ecosystems may be crucial to the survival and stability of prokaryotes in these extreme environments. However, little is known about the interaction between viruses and other mobile genetic elements (MGEs, such as plasmids), and how their interactions influence virus-mediated HGT in these ecosystems. In this study, we adapted a phage-fluorescence in situ hybridization approach to directly monitor the dynamics of phage-plasmid-host interactions at the single-cell level in the Marinitoga piezophila model. Interestingly, our results indicate that plasmid DNA could not only be induced by mitomycin C to a great extent but also hijacked viral assembly machinery to facilitate its propagation and spread. Therefore, the data presented here imply that the interaction between the viruses and other MGEs could play profound roles in virus-host interaction and virus-mediated HGT in the deep-sea hydrothermal ecosystem.
Insights
Mobile genetic elements like plasmids can hijack viruses to spread in deep-sea microbes. This study shows viruses packaging plasmid DNA, revealing molecular piracy in hydrothermal vents and impacting microbial evolution.
Area of Science:
- Microbiology
- Genetics
- Marine Biology
Background:
- Deep-sea hydrothermal vents host diverse microbial communities.
- Mobile genetic elements (MGEs), including viruses and plasmids, drive microbial evolution and horizontal gene transfer (HGT).
- Interactions between MGEs in these extreme environments are poorly understood.
Purpose of the Study:
- To investigate phage-plasmid interactions in the deep-sea bacterium *Marinitoga piezophila*.
- To adapt phage-fluorescence in situ hybridization (phage-FISH) for visualizing these dynamics.
- To understand the role of MGE interactions in virus-mediated HGT in hydrothermal vents.
Main Methods:
- Utilized phage-FISH to monitor phage-plasmid interactions at the single-cell level.
- Induced plasmid replication and packaging using mitomycin C.
- Analyzed DNA content within purified viral particles.
Main Results:
- Plasmid DNA was detected within viral particles released from lysed cells.
- Mitomycin C induced both plasmid replication and packaging into phage particles.
- Phage capsids preferentially packaged plasmid DNA (up to 70%) over viral DNA after induction.
- Plasmid DNA incorporation into phage capsids occurred even without induction.
Conclusions:
- Provided direct evidence of molecular piracy by plasmids in deep-sea hydrothermal ecosystems.
- Demonstrated that plasmids can hijack viral machinery for propagation and spread.
- Highlighted the significant role of selfish MGEs in virus-host interactions and HGT in extreme marine environments.
Related Concept Videos
Plasmids
Bacterial Phylum Proteobacteria
Hyperthermophilic Bacteria
DNA Bacteriophages
Viruses of Archaea
Deep Sea Microbial Ecology

