Phylogenetic relationships of the Wolbachia of nematodes and arthropods.

Wolbachia are well known as bacterial symbionts of arthropods, where they are reproductive parasites, but have also been described from nematode hosts, where the symbiotic interaction has features of mutualism. The majority of arthropod Wolbachia belong to clades A and B, while nematode Wolbachia mo...

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Main Authors: Katelyn Fenn, Claire Conlon, Martin Jones, Michael A Quail, Nancy E Holroyd, Julian Parkhill, Mark Blaxter
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2006-10-01
Series:PLoS Pathogens
Online Access:http://europepmc.org/articles/PMC1599763?pdf=render
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spelling doaj-cf84d7c0c2c341beb97521a02b459c072020-11-24T23:58:44ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742006-10-01210e9410.1371/journal.ppat.0020094Phylogenetic relationships of the Wolbachia of nematodes and arthropods.Katelyn FennClaire ConlonMartin JonesMichael A QuailNancy E HolroydJulian ParkhillMark BlaxterWolbachia are well known as bacterial symbionts of arthropods, where they are reproductive parasites, but have also been described from nematode hosts, where the symbiotic interaction has features of mutualism. The majority of arthropod Wolbachia belong to clades A and B, while nematode Wolbachia mostly belong to clades C and D, but these relationships have been based on analysis of a small number of genes. To investigate the evolution and relationships of Wolbachia symbionts we have sequenced over 70 kb of the genome of wOvo, a Wolbachia from the human-parasitic nematode Onchocerca volvulus, and compared the genes identified to orthologues in other sequenced Wolbachia genomes. In comparisons of conserved local synteny, we find that wBm, from the nematode Brugia malayi, and wMel, from Drosophila melanogaster, are more similar to each other than either is to wOvo. Phylogenetic analysis of the protein-coding and ribosomal RNA genes on the sequenced fragments supports reciprocal monophyly of nematode and arthropod Wolbachia. The nematode Wolbachia did not arise from within the A clade of arthropod Wolbachia, and the root of the Wolbachia clade lies between the nematode and arthropod symbionts. Using the wOvo sequence, we identified a lateral transfer event whereby segments of the Wolbachia genome were inserted into the Onchocerca nuclear genome. This event predated the separation of the human parasite O. volvulus from its cattle-parasitic sister species, O. ochengi. The long association between filarial nematodes and Wolbachia symbionts may permit more frequent genetic exchange between their genomes.http://europepmc.org/articles/PMC1599763?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Katelyn Fenn
Claire Conlon
Martin Jones
Michael A Quail
Nancy E Holroyd
Julian Parkhill
Mark Blaxter
spellingShingle Katelyn Fenn
Claire Conlon
Martin Jones
Michael A Quail
Nancy E Holroyd
Julian Parkhill
Mark Blaxter
Phylogenetic relationships of the Wolbachia of nematodes and arthropods.
PLoS Pathogens
author_facet Katelyn Fenn
Claire Conlon
Martin Jones
Michael A Quail
Nancy E Holroyd
Julian Parkhill
Mark Blaxter
author_sort Katelyn Fenn
title Phylogenetic relationships of the Wolbachia of nematodes and arthropods.
title_short Phylogenetic relationships of the Wolbachia of nematodes and arthropods.
title_full Phylogenetic relationships of the Wolbachia of nematodes and arthropods.
title_fullStr Phylogenetic relationships of the Wolbachia of nematodes and arthropods.
title_full_unstemmed Phylogenetic relationships of the Wolbachia of nematodes and arthropods.
title_sort phylogenetic relationships of the wolbachia of nematodes and arthropods.
publisher Public Library of Science (PLoS)
series PLoS Pathogens
issn 1553-7366
1553-7374
publishDate 2006-10-01
description Wolbachia are well known as bacterial symbionts of arthropods, where they are reproductive parasites, but have also been described from nematode hosts, where the symbiotic interaction has features of mutualism. The majority of arthropod Wolbachia belong to clades A and B, while nematode Wolbachia mostly belong to clades C and D, but these relationships have been based on analysis of a small number of genes. To investigate the evolution and relationships of Wolbachia symbionts we have sequenced over 70 kb of the genome of wOvo, a Wolbachia from the human-parasitic nematode Onchocerca volvulus, and compared the genes identified to orthologues in other sequenced Wolbachia genomes. In comparisons of conserved local synteny, we find that wBm, from the nematode Brugia malayi, and wMel, from Drosophila melanogaster, are more similar to each other than either is to wOvo. Phylogenetic analysis of the protein-coding and ribosomal RNA genes on the sequenced fragments supports reciprocal monophyly of nematode and arthropod Wolbachia. The nematode Wolbachia did not arise from within the A clade of arthropod Wolbachia, and the root of the Wolbachia clade lies between the nematode and arthropod symbionts. Using the wOvo sequence, we identified a lateral transfer event whereby segments of the Wolbachia genome were inserted into the Onchocerca nuclear genome. This event predated the separation of the human parasite O. volvulus from its cattle-parasitic sister species, O. ochengi. The long association between filarial nematodes and Wolbachia symbionts may permit more frequent genetic exchange between their genomes.
url http://europepmc.org/articles/PMC1599763?pdf=render
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