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Prophage maintenance is determined by environment-dependent selective sweeps rather than mutational availability

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Abstract Prophages, viral sequences integrated into bacterial genomes, can be beneficial and costly. Despite the risk of prophage activation and subsequent bacterial death, active prophages are present in most bacterial genomes. However, our understanding of the selective forces that maintain prophages in bacterial populations is limited. Combining experimental evolution with stochastic modelling, we show that prophage maintenance and loss are primarily determined by environmental conditions that alter the net fitness effect of a prophage. When prophages are too costly, they are rapidly lost through environment-specific sequences of selective sweeps. Conflicting selection pressures that select against the prophage but for a prophage-encoded accessory gene can maintain prophages. The dynamics of prophage maintenance additionally depends on the sociality of this accessory gene. Non-cooperative genes maintain prophages at higher frequencies than cooperative genes, which can protect phage-free ‘cheaters’ that may emerge if prophage costs outweigh their benefits. Our simulations suggest that environmental variation plays a larger role than mutation rates in determining prophage maintenance. These findings highlight the complexity of selection pressures that act on mobile genetic elements and challenge our understanding of the role of environmental factors relative to random chance events in shaping the evolutionary trajectory of bacterial populations.
Title: Prophage maintenance is determined by environment-dependent selective sweeps rather than mutational availability
Description:
Abstract Prophages, viral sequences integrated into bacterial genomes, can be beneficial and costly.
Despite the risk of prophage activation and subsequent bacterial death, active prophages are present in most bacterial genomes.
However, our understanding of the selective forces that maintain prophages in bacterial populations is limited.
Combining experimental evolution with stochastic modelling, we show that prophage maintenance and loss are primarily determined by environmental conditions that alter the net fitness effect of a prophage.
When prophages are too costly, they are rapidly lost through environment-specific sequences of selective sweeps.
Conflicting selection pressures that select against the prophage but for a prophage-encoded accessory gene can maintain prophages.
The dynamics of prophage maintenance additionally depends on the sociality of this accessory gene.
Non-cooperative genes maintain prophages at higher frequencies than cooperative genes, which can protect phage-free ‘cheaters’ that may emerge if prophage costs outweigh their benefits.
Our simulations suggest that environmental variation plays a larger role than mutation rates in determining prophage maintenance.
These findings highlight the complexity of selection pressures that act on mobile genetic elements and challenge our understanding of the role of environmental factors relative to random chance events in shaping the evolutionary trajectory of bacterial populations.

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