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Wolbachia springs eternal: symbiosis in Collembola is associated with host ecology

Wolbachia are endosymbiotic alpha-proteobacteria infecting a wide range of arthropods and nematode hosts with diverse interactions, from reproductive parasites to obligate mutualists. Their taxonomy is defined by lineages called supergroups (labelled by letters of the alphabet), while their evolutio...

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Autores principales: Rodrigues, Jules, Lefoulon, Emilie, Gavotte, Laurent, Perillat-Sanguinet, Marco, Makepeace, Benjamin, Martin, Coralie, D'Haese, Cyrille A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10230187/
https://www.ncbi.nlm.nih.gov/pubmed/37266040
http://dx.doi.org/10.1098/rsos.230288
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author Rodrigues, Jules
Lefoulon, Emilie
Gavotte, Laurent
Perillat-Sanguinet, Marco
Makepeace, Benjamin
Martin, Coralie
D'Haese, Cyrille A.
author_facet Rodrigues, Jules
Lefoulon, Emilie
Gavotte, Laurent
Perillat-Sanguinet, Marco
Makepeace, Benjamin
Martin, Coralie
D'Haese, Cyrille A.
author_sort Rodrigues, Jules
collection PubMed
description Wolbachia are endosymbiotic alpha-proteobacteria infecting a wide range of arthropods and nematode hosts with diverse interactions, from reproductive parasites to obligate mutualists. Their taxonomy is defined by lineages called supergroups (labelled by letters of the alphabet), while their evolutionary history is complex, with multiple horizontal transfers and secondary losses. One of the least recently derived, supergroup E, infects springtails (Collembola), widely distributed hexapods, with sexual and/or parthenogenetic populations depending on species. To better characterize the diversity of Wolbachia infecting springtails, the presence of Wolbachia was screened in 58 species. Eleven (20%) species were found to be positive, with three Wolbachia genotypes identified for the first time in supergroup A. The novel genotypes infect springtails ecologically and biologically different from those infected by supergroup E. To root the Wolbachia phylogeny, rather than distant other Rickettsiales, supergroup L infecting plant-parasitic nematodes was used here. We hypothesize that the ancestor of Wolbachia was consumed by soil-dwelling nematodes, and was transferred horizontally via plants into aphids, which then infected edaphic arthropods (e.g. springtails and oribatid mites) before expanding into most clades of terrestrial arthropods and filarial nematodes.
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spelling pubmed-102301872023-06-01 Wolbachia springs eternal: symbiosis in Collembola is associated with host ecology Rodrigues, Jules Lefoulon, Emilie Gavotte, Laurent Perillat-Sanguinet, Marco Makepeace, Benjamin Martin, Coralie D'Haese, Cyrille A. R Soc Open Sci Organismal and Evolutionary Biology Wolbachia are endosymbiotic alpha-proteobacteria infecting a wide range of arthropods and nematode hosts with diverse interactions, from reproductive parasites to obligate mutualists. Their taxonomy is defined by lineages called supergroups (labelled by letters of the alphabet), while their evolutionary history is complex, with multiple horizontal transfers and secondary losses. One of the least recently derived, supergroup E, infects springtails (Collembola), widely distributed hexapods, with sexual and/or parthenogenetic populations depending on species. To better characterize the diversity of Wolbachia infecting springtails, the presence of Wolbachia was screened in 58 species. Eleven (20%) species were found to be positive, with three Wolbachia genotypes identified for the first time in supergroup A. The novel genotypes infect springtails ecologically and biologically different from those infected by supergroup E. To root the Wolbachia phylogeny, rather than distant other Rickettsiales, supergroup L infecting plant-parasitic nematodes was used here. We hypothesize that the ancestor of Wolbachia was consumed by soil-dwelling nematodes, and was transferred horizontally via plants into aphids, which then infected edaphic arthropods (e.g. springtails and oribatid mites) before expanding into most clades of terrestrial arthropods and filarial nematodes. The Royal Society 2023-05-31 /pmc/articles/PMC10230187/ /pubmed/37266040 http://dx.doi.org/10.1098/rsos.230288 Text en © 2023 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Organismal and Evolutionary Biology
Rodrigues, Jules
Lefoulon, Emilie
Gavotte, Laurent
Perillat-Sanguinet, Marco
Makepeace, Benjamin
Martin, Coralie
D'Haese, Cyrille A.
Wolbachia springs eternal: symbiosis in Collembola is associated with host ecology
title Wolbachia springs eternal: symbiosis in Collembola is associated with host ecology
title_full Wolbachia springs eternal: symbiosis in Collembola is associated with host ecology
title_fullStr Wolbachia springs eternal: symbiosis in Collembola is associated with host ecology
title_full_unstemmed Wolbachia springs eternal: symbiosis in Collembola is associated with host ecology
title_short Wolbachia springs eternal: symbiosis in Collembola is associated with host ecology
title_sort wolbachia springs eternal: symbiosis in collembola is associated with host ecology
topic Organismal and Evolutionary Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10230187/
https://www.ncbi.nlm.nih.gov/pubmed/37266040
http://dx.doi.org/10.1098/rsos.230288
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