Abstract

Bacterial genomes are highly plastic allowing the generation of variants through mutations and acquisition of genetic information. The fittest variants are then selected by the econiche thereby allowing the bacterial adaptation and colonization of the habitat. Larger genomes, however, may impose metabolic burden and hence bacterial genomes are optimized by the loss of frivolous genetic information. The activity of temperate bacteriophages has acute consequences on the bacterial population as well as the bacterial genome through lytic and lysogenic cycles. Lysogeny is a selective advantage as the prophage provides immunity to the lysogen against secondary phage attack. Since the non-lysogens are eliminated by the lytic phages, lysogens multiply and colonize the habitat. Nevertheless, all lysogens have an imminent risk of lytic cycle activation and cell lysis. However, a mutation in the attachment sites or in the genes that encode the specific recombinase responsible for prophage excision could result in ‘grounding’ of the prophage. Since the lysogens with grounded prophage are immune to respective phage infection as well as dodge the induction of lytic cycle, we hypothesize that the selection of these mutant lysogens is favored relative to their normal lysogenic counterparts. These grounded prophages offer several advantages to the bacterial genome evolution through propensity for genetic variations including inversions, deletions, and insertions via horizontal gene transfer. We propose that the grounded prophages expedite bacterial genome evolution by acting as ‘genetic buffer zones’ thereby increasing the frequency as well as the diversity of variations on which natural selection favors the beneficial variants. The grounded prophages are also hotspots for horizontal gene transfer wherein several ecologically significant genes such as those involved in stress tolerance, antimicrobial resistance, and novel metabolic pathways, are integrated. Moreover, the high frequency of genetic changes within prophages also allows proportionate probability for the de novo genesis of genetic information. Through sequence analyses of well-characterized E. coli prophages we exemplify various roles of grounded prophages in E. coli ecology and evolution. Therefore, the temperate prophages are one of the most significant drivers of bacterial genome evolution and sites of biogenesis of genetic information.

Highlights

  • Genome plasticity is an essential requirement for evolution directed by ‘econiche.’ Bacterial genomes are highly plastic relative to other organisms owing to the diversity and dynamicity of the niche (Dobrindt et al, 2010)

  • In Ralstonia solanacearum the attB site for φRSA1 prophage integration occurred downstream of the tRNA-Arg gene (Fujiwara et al, 2008) and in E. coli, the relatives of λ phage and P4 phage insert within the tRNA genes (Campbell, 2003). It is rational for a phage with a broader range of host specificity to prefer integration sites that are within protein-coding functional genes as their occurrence is conserved across distantly related species, subject to the tolerable consequences of the recombination (Hill et al, 1989)

  • To predict the possible role of the cryptic prophage in contributing to the ecological advantages to the host bacterium, we manually scouted for genes that are unrelated to the phage/plasmid in the Qin prophages of various E. coli strains [Supplementary Table S3 (Datasheet S2)]

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Summary

Introduction

Genome plasticity is an essential requirement for evolution directed by ‘econiche.’ Bacterial genomes are highly plastic relative to other organisms owing to the diversity and dynamicity of the niche (Dobrindt et al, 2010). It is rational for a phage with a broader range of host specificity to prefer integration sites that are within protein-coding functional genes as their occurrence is conserved across distantly related species, subject to the tolerable consequences of the recombination (Hill et al, 1989).

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