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Polyclonality of Concurrent Natural Populations of Alteromonas macleodii

We have analyzed a natural population of the marine bacterium, Alteromonas macleodii, from a single sample of seawater to evaluate the genomic diversity present. We performed full genome sequencing of four isolates and 161 metagenomic fosmid clones, all of which were assigned to A. macleodii by sequ...

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Autores principales: Gonzaga, Aitor, Martin-Cuadrado, Ana-Belen, López-Pérez, Mario, Megumi Mizuno, Carolina, García-Heredia, Inmaculada, Kimes, Nikole E., Lopez-García, Purificación, Moreira, David, Ussery, David, Zaballos, Mila, Ghai, Rohit, Rodriguez-Valera, Francisco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3542563/
https://www.ncbi.nlm.nih.gov/pubmed/23212172
http://dx.doi.org/10.1093/gbe/evs112
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author Gonzaga, Aitor
Martin-Cuadrado, Ana-Belen
López-Pérez, Mario
Megumi Mizuno, Carolina
García-Heredia, Inmaculada
Kimes, Nikole E.
Lopez-García, Purificación
Moreira, David
Ussery, David
Zaballos, Mila
Ghai, Rohit
Rodriguez-Valera, Francisco
author_facet Gonzaga, Aitor
Martin-Cuadrado, Ana-Belen
López-Pérez, Mario
Megumi Mizuno, Carolina
García-Heredia, Inmaculada
Kimes, Nikole E.
Lopez-García, Purificación
Moreira, David
Ussery, David
Zaballos, Mila
Ghai, Rohit
Rodriguez-Valera, Francisco
author_sort Gonzaga, Aitor
collection PubMed
description We have analyzed a natural population of the marine bacterium, Alteromonas macleodii, from a single sample of seawater to evaluate the genomic diversity present. We performed full genome sequencing of four isolates and 161 metagenomic fosmid clones, all of which were assigned to A. macleodii by sequence similarity. Out of the four strain genomes, A. macleodii deep ecotype (AltDE1) represented a different genome, whereas AltDE2 and AltDE3 were identical to the previously described AltDE. Although the core genome (∼80%) had an average nucleotide identity of 98.51%, both AltDE and AltDE1 contained flexible genomic islands (fGIs), that is, genomic islands present in both genomes in the same genomic context but having different gene content. Some of the fGIs encode cell surface receptors known to be phage recognition targets, such as the O-chain of the lipopolysaccharide, whereas others have genes involved in physiological traits (e.g., nutrient transport, degradation, and metal resistance) denoting microniche specialization. The presence in metagenomic fosmids of genomic fragments differing from the sequenced strain genomes, together with the presence of new fGIs, indicates that there are at least two more A. macleodii clones present. The availability of three or more sequences overlapping the same genomic region also allowed us to estimate the frequency and distribution of recombination events among these different clones, indicating that these clustered near the genomic islands. The results indicate that this natural A. macleodii population has multiple clones with a potential for different phage susceptibility and exploitation of resources, within a seemingly unstructured habitat.
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spelling pubmed-35425632013-01-11 Polyclonality of Concurrent Natural Populations of Alteromonas macleodii Gonzaga, Aitor Martin-Cuadrado, Ana-Belen López-Pérez, Mario Megumi Mizuno, Carolina García-Heredia, Inmaculada Kimes, Nikole E. Lopez-García, Purificación Moreira, David Ussery, David Zaballos, Mila Ghai, Rohit Rodriguez-Valera, Francisco Genome Biol Evol Research Article We have analyzed a natural population of the marine bacterium, Alteromonas macleodii, from a single sample of seawater to evaluate the genomic diversity present. We performed full genome sequencing of four isolates and 161 metagenomic fosmid clones, all of which were assigned to A. macleodii by sequence similarity. Out of the four strain genomes, A. macleodii deep ecotype (AltDE1) represented a different genome, whereas AltDE2 and AltDE3 were identical to the previously described AltDE. Although the core genome (∼80%) had an average nucleotide identity of 98.51%, both AltDE and AltDE1 contained flexible genomic islands (fGIs), that is, genomic islands present in both genomes in the same genomic context but having different gene content. Some of the fGIs encode cell surface receptors known to be phage recognition targets, such as the O-chain of the lipopolysaccharide, whereas others have genes involved in physiological traits (e.g., nutrient transport, degradation, and metal resistance) denoting microniche specialization. The presence in metagenomic fosmids of genomic fragments differing from the sequenced strain genomes, together with the presence of new fGIs, indicates that there are at least two more A. macleodii clones present. The availability of three or more sequences overlapping the same genomic region also allowed us to estimate the frequency and distribution of recombination events among these different clones, indicating that these clustered near the genomic islands. The results indicate that this natural A. macleodii population has multiple clones with a potential for different phage susceptibility and exploitation of resources, within a seemingly unstructured habitat. Oxford University Press 2012 2012-12-03 /pmc/articles/PMC3542563/ /pubmed/23212172 http://dx.doi.org/10.1093/gbe/evs112 Text en © The Author(s) 2012. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Gonzaga, Aitor
Martin-Cuadrado, Ana-Belen
López-Pérez, Mario
Megumi Mizuno, Carolina
García-Heredia, Inmaculada
Kimes, Nikole E.
Lopez-García, Purificación
Moreira, David
Ussery, David
Zaballos, Mila
Ghai, Rohit
Rodriguez-Valera, Francisco
Polyclonality of Concurrent Natural Populations of Alteromonas macleodii
title Polyclonality of Concurrent Natural Populations of Alteromonas macleodii
title_full Polyclonality of Concurrent Natural Populations of Alteromonas macleodii
title_fullStr Polyclonality of Concurrent Natural Populations of Alteromonas macleodii
title_full_unstemmed Polyclonality of Concurrent Natural Populations of Alteromonas macleodii
title_short Polyclonality of Concurrent Natural Populations of Alteromonas macleodii
title_sort polyclonality of concurrent natural populations of alteromonas macleodii
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3542563/
https://www.ncbi.nlm.nih.gov/pubmed/23212172
http://dx.doi.org/10.1093/gbe/evs112
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