Cargando…
Draft Genomes, Phylogenetic Reconstruction, and Comparative Genomics of Two Novel Cohabiting Bacterial Symbionts Isolated from Frankliniella occidentalis
Obligate bacterial symbionts are widespread in many invertebrates, where they are often confined to specialized host cells and are transmitted directly from mother to progeny. Increasing numbers of these bacteria are being characterized but questions remain about their population structure and evolu...
Autores principales: | , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4558854/ https://www.ncbi.nlm.nih.gov/pubmed/26185096 http://dx.doi.org/10.1093/gbe/evv136 |
_version_ | 1782388682438737920 |
---|---|
author | Facey, Paul D. Méric, Guillaume Hitchings, Matthew D. Pachebat, Justin A. Hegarty, Matt J. Chen, Xiaorui Morgan, Laura V.A. Hoeppner, James E. Whitten, Miranda M.A. Kirk, William D.J. Dyson, Paul J. Sheppard, Sam K. Sol, Ricardo Del |
author_facet | Facey, Paul D. Méric, Guillaume Hitchings, Matthew D. Pachebat, Justin A. Hegarty, Matt J. Chen, Xiaorui Morgan, Laura V.A. Hoeppner, James E. Whitten, Miranda M.A. Kirk, William D.J. Dyson, Paul J. Sheppard, Sam K. Sol, Ricardo Del |
author_sort | Facey, Paul D. |
collection | PubMed |
description | Obligate bacterial symbionts are widespread in many invertebrates, where they are often confined to specialized host cells and are transmitted directly from mother to progeny. Increasing numbers of these bacteria are being characterized but questions remain about their population structure and evolution. Here we take a comparative genomics approach to investigate two prominent bacterial symbionts (BFo1 and BFo2) isolated from geographically separated populations of western flower thrips, Frankliniella occidentalis. Our multifaceted approach to classifying these symbionts includes concatenated multilocus sequence analysis (MLSA) phylogenies, ribosomal multilocus sequence typing (rMLST), construction of whole-genome phylogenies, and in-depth genomic comparisons. We showed that the BFo1 genome clusters more closely to species in the genus Erwinia, and is a putative close relative to Erwinia aphidicola. BFo1 is also likely to have shared a common ancestor with Erwinia pyrifoliae/Erwinia amylovora and the nonpathogenic Erwinia tasmaniensis and genetic traits similar to Erwinia billingiae. The BFo1 genome contained virulence factors found in the genus Erwinia but represented a divergent lineage. In contrast, we showed that BFo2 belongs within the Enterobacteriales but does not group closely with any currently known bacterial species. Concatenated MLSA phylogenies indicate that it may have shared a common ancestor to the Erwinia and Pantoea genera, and based on the clustering of rMLST genes, it was most closely related to Pantoea ananatis but represented a divergent lineage. We reconstructed a core genome of a putative common ancestor of Erwinia and Pantoea and compared this with the genomes of BFo bacteria. BFo2 possessed none of the virulence determinants that were omnipresent in the Erwinia and Pantoea genera. Taken together, these data are consistent with BFo2 representing a highly novel species that maybe related to known Pantoea. |
format | Online Article Text |
id | pubmed-4558854 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-45588542015-09-08 Draft Genomes, Phylogenetic Reconstruction, and Comparative Genomics of Two Novel Cohabiting Bacterial Symbionts Isolated from Frankliniella occidentalis Facey, Paul D. Méric, Guillaume Hitchings, Matthew D. Pachebat, Justin A. Hegarty, Matt J. Chen, Xiaorui Morgan, Laura V.A. Hoeppner, James E. Whitten, Miranda M.A. Kirk, William D.J. Dyson, Paul J. Sheppard, Sam K. Sol, Ricardo Del Genome Biol Evol Research Article Obligate bacterial symbionts are widespread in many invertebrates, where they are often confined to specialized host cells and are transmitted directly from mother to progeny. Increasing numbers of these bacteria are being characterized but questions remain about their population structure and evolution. Here we take a comparative genomics approach to investigate two prominent bacterial symbionts (BFo1 and BFo2) isolated from geographically separated populations of western flower thrips, Frankliniella occidentalis. Our multifaceted approach to classifying these symbionts includes concatenated multilocus sequence analysis (MLSA) phylogenies, ribosomal multilocus sequence typing (rMLST), construction of whole-genome phylogenies, and in-depth genomic comparisons. We showed that the BFo1 genome clusters more closely to species in the genus Erwinia, and is a putative close relative to Erwinia aphidicola. BFo1 is also likely to have shared a common ancestor with Erwinia pyrifoliae/Erwinia amylovora and the nonpathogenic Erwinia tasmaniensis and genetic traits similar to Erwinia billingiae. The BFo1 genome contained virulence factors found in the genus Erwinia but represented a divergent lineage. In contrast, we showed that BFo2 belongs within the Enterobacteriales but does not group closely with any currently known bacterial species. Concatenated MLSA phylogenies indicate that it may have shared a common ancestor to the Erwinia and Pantoea genera, and based on the clustering of rMLST genes, it was most closely related to Pantoea ananatis but represented a divergent lineage. We reconstructed a core genome of a putative common ancestor of Erwinia and Pantoea and compared this with the genomes of BFo bacteria. BFo2 possessed none of the virulence determinants that were omnipresent in the Erwinia and Pantoea genera. Taken together, these data are consistent with BFo2 representing a highly novel species that maybe related to known Pantoea. Oxford University Press 2015-07-21 /pmc/articles/PMC4558854/ /pubmed/26185096 http://dx.doi.org/10.1093/gbe/evv136 Text en © The Author(s) 2015. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Facey, Paul D. Méric, Guillaume Hitchings, Matthew D. Pachebat, Justin A. Hegarty, Matt J. Chen, Xiaorui Morgan, Laura V.A. Hoeppner, James E. Whitten, Miranda M.A. Kirk, William D.J. Dyson, Paul J. Sheppard, Sam K. Sol, Ricardo Del Draft Genomes, Phylogenetic Reconstruction, and Comparative Genomics of Two Novel Cohabiting Bacterial Symbionts Isolated from Frankliniella occidentalis |
title | Draft Genomes, Phylogenetic Reconstruction, and Comparative Genomics of Two Novel Cohabiting Bacterial Symbionts Isolated from Frankliniella occidentalis |
title_full | Draft Genomes, Phylogenetic Reconstruction, and Comparative Genomics of Two Novel Cohabiting Bacterial Symbionts Isolated from Frankliniella occidentalis |
title_fullStr | Draft Genomes, Phylogenetic Reconstruction, and Comparative Genomics of Two Novel Cohabiting Bacterial Symbionts Isolated from Frankliniella occidentalis |
title_full_unstemmed | Draft Genomes, Phylogenetic Reconstruction, and Comparative Genomics of Two Novel Cohabiting Bacterial Symbionts Isolated from Frankliniella occidentalis |
title_short | Draft Genomes, Phylogenetic Reconstruction, and Comparative Genomics of Two Novel Cohabiting Bacterial Symbionts Isolated from Frankliniella occidentalis |
title_sort | draft genomes, phylogenetic reconstruction, and comparative genomics of two novel cohabiting bacterial symbionts isolated from frankliniella occidentalis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4558854/ https://www.ncbi.nlm.nih.gov/pubmed/26185096 http://dx.doi.org/10.1093/gbe/evv136 |
work_keys_str_mv | AT faceypauld draftgenomesphylogeneticreconstructionandcomparativegenomicsoftwonovelcohabitingbacterialsymbiontsisolatedfromfrankliniellaoccidentalis AT mericguillaume draftgenomesphylogeneticreconstructionandcomparativegenomicsoftwonovelcohabitingbacterialsymbiontsisolatedfromfrankliniellaoccidentalis AT hitchingsmatthewd draftgenomesphylogeneticreconstructionandcomparativegenomicsoftwonovelcohabitingbacterialsymbiontsisolatedfromfrankliniellaoccidentalis AT pachebatjustina draftgenomesphylogeneticreconstructionandcomparativegenomicsoftwonovelcohabitingbacterialsymbiontsisolatedfromfrankliniellaoccidentalis AT hegartymattj draftgenomesphylogeneticreconstructionandcomparativegenomicsoftwonovelcohabitingbacterialsymbiontsisolatedfromfrankliniellaoccidentalis AT chenxiaorui draftgenomesphylogeneticreconstructionandcomparativegenomicsoftwonovelcohabitingbacterialsymbiontsisolatedfromfrankliniellaoccidentalis AT morganlaurava draftgenomesphylogeneticreconstructionandcomparativegenomicsoftwonovelcohabitingbacterialsymbiontsisolatedfromfrankliniellaoccidentalis AT hoeppnerjamese draftgenomesphylogeneticreconstructionandcomparativegenomicsoftwonovelcohabitingbacterialsymbiontsisolatedfromfrankliniellaoccidentalis AT whittenmirandama draftgenomesphylogeneticreconstructionandcomparativegenomicsoftwonovelcohabitingbacterialsymbiontsisolatedfromfrankliniellaoccidentalis AT kirkwilliamdj draftgenomesphylogeneticreconstructionandcomparativegenomicsoftwonovelcohabitingbacterialsymbiontsisolatedfromfrankliniellaoccidentalis AT dysonpaulj draftgenomesphylogeneticreconstructionandcomparativegenomicsoftwonovelcohabitingbacterialsymbiontsisolatedfromfrankliniellaoccidentalis AT sheppardsamk draftgenomesphylogeneticreconstructionandcomparativegenomicsoftwonovelcohabitingbacterialsymbiontsisolatedfromfrankliniellaoccidentalis AT solricardodel draftgenomesphylogeneticreconstructionandcomparativegenomicsoftwonovelcohabitingbacterialsymbiontsisolatedfromfrankliniellaoccidentalis |