Cargando…
Population Genomics and Phylogeography of an Australian Dairy Factory Derived Lytic Bacteriophage
In this study, we present the full genomic sequences and evolutionary analyses of a serially sampled population of 28 Lactococcus lactis–infecting phage belonging to the 936-like group in Australia. Genome sizes were consistent with previously available genomes ranging in length from 30.9 to 32.1 Kb...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3318435/ https://www.ncbi.nlm.nih.gov/pubmed/22355195 http://dx.doi.org/10.1093/gbe/evs017 |
_version_ | 1782228691234848768 |
---|---|
author | Castro-Nallar, Eduardo Chen, Honglei Gladman, Simon Moore, Sean C. Seemann, Torsten Powell, Ian B. Hillier, Alan Crandall, Keith A. Chandry, P. Scott |
author_facet | Castro-Nallar, Eduardo Chen, Honglei Gladman, Simon Moore, Sean C. Seemann, Torsten Powell, Ian B. Hillier, Alan Crandall, Keith A. Chandry, P. Scott |
author_sort | Castro-Nallar, Eduardo |
collection | PubMed |
description | In this study, we present the full genomic sequences and evolutionary analyses of a serially sampled population of 28 Lactococcus lactis–infecting phage belonging to the 936-like group in Australia. Genome sizes were consistent with previously available genomes ranging in length from 30.9 to 32.1 Kbp and consisted of 55–65 open reading frames. We analyzed their genetic diversity and found that regions of high diversity are correlated with high recombination rate regions (P value = 0.01). Phylogenetic inference showed two major clades that correlate well with known host range. Using the extended Bayesian Skyline model, we found that population size has remained mostly constant through time. Moreover, the dispersion pattern of these genomes is in agreement with human-driven dispersion as suggested by phylogeographic analysis. In addition, selection analysis found evidence of positive selection on codon positions of the Receptor Binding Protein (RBP). Likewise, positively selected sites in the RBP were located within the neck and head region in the crystal structure, both known determinants of host range. Our study demonstrates the utility of phylogenetic methods applied to whole genome data collected from populations of phage for providing insights into applied microbiology. |
format | Online Article Text |
id | pubmed-3318435 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-33184352012-04-04 Population Genomics and Phylogeography of an Australian Dairy Factory Derived Lytic Bacteriophage Castro-Nallar, Eduardo Chen, Honglei Gladman, Simon Moore, Sean C. Seemann, Torsten Powell, Ian B. Hillier, Alan Crandall, Keith A. Chandry, P. Scott Genome Biol Evol Research Articles In this study, we present the full genomic sequences and evolutionary analyses of a serially sampled population of 28 Lactococcus lactis–infecting phage belonging to the 936-like group in Australia. Genome sizes were consistent with previously available genomes ranging in length from 30.9 to 32.1 Kbp and consisted of 55–65 open reading frames. We analyzed their genetic diversity and found that regions of high diversity are correlated with high recombination rate regions (P value = 0.01). Phylogenetic inference showed two major clades that correlate well with known host range. Using the extended Bayesian Skyline model, we found that population size has remained mostly constant through time. Moreover, the dispersion pattern of these genomes is in agreement with human-driven dispersion as suggested by phylogeographic analysis. In addition, selection analysis found evidence of positive selection on codon positions of the Receptor Binding Protein (RBP). Likewise, positively selected sites in the RBP were located within the neck and head region in the crystal structure, both known determinants of host range. Our study demonstrates the utility of phylogenetic methods applied to whole genome data collected from populations of phage for providing insights into applied microbiology. Oxford University Press 2012 2012-02-21 /pmc/articles/PMC3318435/ /pubmed/22355195 http://dx.doi.org/10.1093/gbe/evs017 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 Articles Castro-Nallar, Eduardo Chen, Honglei Gladman, Simon Moore, Sean C. Seemann, Torsten Powell, Ian B. Hillier, Alan Crandall, Keith A. Chandry, P. Scott Population Genomics and Phylogeography of an Australian Dairy Factory Derived Lytic Bacteriophage |
title | Population Genomics and Phylogeography of an Australian Dairy Factory Derived Lytic Bacteriophage |
title_full | Population Genomics and Phylogeography of an Australian Dairy Factory Derived Lytic Bacteriophage |
title_fullStr | Population Genomics and Phylogeography of an Australian Dairy Factory Derived Lytic Bacteriophage |
title_full_unstemmed | Population Genomics and Phylogeography of an Australian Dairy Factory Derived Lytic Bacteriophage |
title_short | Population Genomics and Phylogeography of an Australian Dairy Factory Derived Lytic Bacteriophage |
title_sort | population genomics and phylogeography of an australian dairy factory derived lytic bacteriophage |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3318435/ https://www.ncbi.nlm.nih.gov/pubmed/22355195 http://dx.doi.org/10.1093/gbe/evs017 |
work_keys_str_mv | AT castronallareduardo populationgenomicsandphylogeographyofanaustraliandairyfactoryderivedlyticbacteriophage AT chenhonglei populationgenomicsandphylogeographyofanaustraliandairyfactoryderivedlyticbacteriophage AT gladmansimon populationgenomicsandphylogeographyofanaustraliandairyfactoryderivedlyticbacteriophage AT mooreseanc populationgenomicsandphylogeographyofanaustraliandairyfactoryderivedlyticbacteriophage AT seemanntorsten populationgenomicsandphylogeographyofanaustraliandairyfactoryderivedlyticbacteriophage AT powellianb populationgenomicsandphylogeographyofanaustraliandairyfactoryderivedlyticbacteriophage AT hillieralan populationgenomicsandphylogeographyofanaustraliandairyfactoryderivedlyticbacteriophage AT crandallkeitha populationgenomicsandphylogeographyofanaustraliandairyfactoryderivedlyticbacteriophage AT chandrypscott populationgenomicsandphylogeographyofanaustraliandairyfactoryderivedlyticbacteriophage |