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Bacterial ‘Grounded’ Prophages: Hotspots for Genetic Renovation and Innovation

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 met...

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Autores principales: Ramisetty, Bhaskar Chandra Mohan, Sudhakari, Pavithra Anantharaman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6379469/
https://www.ncbi.nlm.nih.gov/pubmed/30809245
http://dx.doi.org/10.3389/fgene.2019.00065
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author Ramisetty, Bhaskar Chandra Mohan
Sudhakari, Pavithra Anantharaman
author_facet Ramisetty, Bhaskar Chandra Mohan
Sudhakari, Pavithra Anantharaman
author_sort Ramisetty, Bhaskar Chandra Mohan
collection PubMed
description 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.
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spelling pubmed-63794692019-02-26 Bacterial ‘Grounded’ Prophages: Hotspots for Genetic Renovation and Innovation Ramisetty, Bhaskar Chandra Mohan Sudhakari, Pavithra Anantharaman Front Genet Genetics 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. Frontiers Media S.A. 2019-02-12 /pmc/articles/PMC6379469/ /pubmed/30809245 http://dx.doi.org/10.3389/fgene.2019.00065 Text en Copyright © 2019 Ramisetty and Sudhakari. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Ramisetty, Bhaskar Chandra Mohan
Sudhakari, Pavithra Anantharaman
Bacterial ‘Grounded’ Prophages: Hotspots for Genetic Renovation and Innovation
title Bacterial ‘Grounded’ Prophages: Hotspots for Genetic Renovation and Innovation
title_full Bacterial ‘Grounded’ Prophages: Hotspots for Genetic Renovation and Innovation
title_fullStr Bacterial ‘Grounded’ Prophages: Hotspots for Genetic Renovation and Innovation
title_full_unstemmed Bacterial ‘Grounded’ Prophages: Hotspots for Genetic Renovation and Innovation
title_short Bacterial ‘Grounded’ Prophages: Hotspots for Genetic Renovation and Innovation
title_sort bacterial ‘grounded’ prophages: hotspots for genetic renovation and innovation
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6379469/
https://www.ncbi.nlm.nih.gov/pubmed/30809245
http://dx.doi.org/10.3389/fgene.2019.00065
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