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Dynamics of genome evolution in facultative symbionts of aphids
Aphids are sap-feeding insects that host a range of bacterial endosymbionts including the obligate, nutritional mutualist Buchnera plus several bacteria that are not required for host survival. Among the latter, ‘Candidatus Regiella insecticola’ and ‘Candidatus Hamiltonella defensa’ are found in pea...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Blackwell Publishing Ltd
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2955975/ https://www.ncbi.nlm.nih.gov/pubmed/21966902 http://dx.doi.org/10.1111/j.1462-2920.2009.02085.x |
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author | Degnan, Patrick H Leonardo, Teresa E Cass, Bodil N Hurwitz, Bonnie Stern, David Gibbs, Richard A Richards, Stephen Moran, Nancy A |
author_facet | Degnan, Patrick H Leonardo, Teresa E Cass, Bodil N Hurwitz, Bonnie Stern, David Gibbs, Richard A Richards, Stephen Moran, Nancy A |
author_sort | Degnan, Patrick H |
collection | PubMed |
description | Aphids are sap-feeding insects that host a range of bacterial endosymbionts including the obligate, nutritional mutualist Buchnera plus several bacteria that are not required for host survival. Among the latter, ‘Candidatus Regiella insecticola’ and ‘Candidatus Hamiltonella defensa’ are found in pea aphids and other hosts and have been shown to protect aphids from natural enemies. We have sequenced almost the entire genome of R. insecticola (2.07 Mbp) and compared it with the recently published genome of H. defensa (2.11 Mbp). Despite being sister species the two genomes are highly rearranged and the genomes only have ∼55% of genes in common. The functions encoded by the shared genes imply that the bacteria have similar metabolic capabilities, including only two essential amino acid biosynthetic pathways and active uptake mechanisms for the remaining eight, and similar capacities for host cell toxicity and invasion (type 3 secretion systems and RTX toxins). These observations, combined with high sequence divergence of orthologues, strongly suggest an ancient divergence after establishment of a symbiotic lifestyle. The divergence in gene sets and in genome architecture implies a history of rampant recombination and gene inactivation and the ongoing integration of mobile DNA (insertion sequence elements, prophage and plasmids). |
format | Text |
id | pubmed-2955975 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-29559752010-10-23 Dynamics of genome evolution in facultative symbionts of aphids Degnan, Patrick H Leonardo, Teresa E Cass, Bodil N Hurwitz, Bonnie Stern, David Gibbs, Richard A Richards, Stephen Moran, Nancy A Environ Microbiol Research Articles Aphids are sap-feeding insects that host a range of bacterial endosymbionts including the obligate, nutritional mutualist Buchnera plus several bacteria that are not required for host survival. Among the latter, ‘Candidatus Regiella insecticola’ and ‘Candidatus Hamiltonella defensa’ are found in pea aphids and other hosts and have been shown to protect aphids from natural enemies. We have sequenced almost the entire genome of R. insecticola (2.07 Mbp) and compared it with the recently published genome of H. defensa (2.11 Mbp). Despite being sister species the two genomes are highly rearranged and the genomes only have ∼55% of genes in common. The functions encoded by the shared genes imply that the bacteria have similar metabolic capabilities, including only two essential amino acid biosynthetic pathways and active uptake mechanisms for the remaining eight, and similar capacities for host cell toxicity and invasion (type 3 secretion systems and RTX toxins). These observations, combined with high sequence divergence of orthologues, strongly suggest an ancient divergence after establishment of a symbiotic lifestyle. The divergence in gene sets and in genome architecture implies a history of rampant recombination and gene inactivation and the ongoing integration of mobile DNA (insertion sequence elements, prophage and plasmids). Blackwell Publishing Ltd 2010-08 /pmc/articles/PMC2955975/ /pubmed/21966902 http://dx.doi.org/10.1111/j.1462-2920.2009.02085.x Text en © 2010 Society for Applied Microbiology and Blackwell Publishing Ltd http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
spellingShingle | Research Articles Degnan, Patrick H Leonardo, Teresa E Cass, Bodil N Hurwitz, Bonnie Stern, David Gibbs, Richard A Richards, Stephen Moran, Nancy A Dynamics of genome evolution in facultative symbionts of aphids |
title | Dynamics of genome evolution in facultative symbionts of aphids |
title_full | Dynamics of genome evolution in facultative symbionts of aphids |
title_fullStr | Dynamics of genome evolution in facultative symbionts of aphids |
title_full_unstemmed | Dynamics of genome evolution in facultative symbionts of aphids |
title_short | Dynamics of genome evolution in facultative symbionts of aphids |
title_sort | dynamics of genome evolution in facultative symbionts of aphids |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2955975/ https://www.ncbi.nlm.nih.gov/pubmed/21966902 http://dx.doi.org/10.1111/j.1462-2920.2009.02085.x |
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