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Highly transmissible cytoplasmic incompatibility by the extracellular insect symbiont Spiroplasma
Cytoplasmic incompatibility (CI) is a form of reproductive manipulation caused by maternally inherited endosymbionts infecting arthropods, like Wolbachia, whereby matings between infected males and uninfected females produce few or no offspring. We report the discovery of a new CI symbiont, a strain...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9118660/ https://www.ncbi.nlm.nih.gov/pubmed/35602967 http://dx.doi.org/10.1016/j.isci.2022.104335 |
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author | Pollmann, Marie Moore, Logan D. Krimmer, Elena D'Alvise, Paul Hasselmann, Martin Perlman, Steve J. Ballinger, Matthew J. Steidle, Johannes L.M. Gottlieb, Yuval |
author_facet | Pollmann, Marie Moore, Logan D. Krimmer, Elena D'Alvise, Paul Hasselmann, Martin Perlman, Steve J. Ballinger, Matthew J. Steidle, Johannes L.M. Gottlieb, Yuval |
author_sort | Pollmann, Marie |
collection | PubMed |
description | Cytoplasmic incompatibility (CI) is a form of reproductive manipulation caused by maternally inherited endosymbionts infecting arthropods, like Wolbachia, whereby matings between infected males and uninfected females produce few or no offspring. We report the discovery of a new CI symbiont, a strain of Spiroplasma causing CI in the parasitoid wasp Lariophagus distinguendus. Its extracellular occurrence enabled us to establish CI in uninfected adult insects by transferring Spiroplasma-infected hemolymph. We sequenced the CI-Spiroplasma genome and did not find any homologues of any of the cif genes discovered to cause CI in Wolbachia, suggesting independent evolution of CI. Instead, the genome contains other potential CI-causing candidate genes, such as homologues of high-mobility group (HMG) box proteins that are crucial in eukaryotic development but rare in bacterial genomes. Spiroplasma’s extracellular nature and broad host range encompassing medically and agriculturally important arthropods make it a promising tool to study CI and its applications. |
format | Online Article Text |
id | pubmed-9118660 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-91186602022-05-20 Highly transmissible cytoplasmic incompatibility by the extracellular insect symbiont Spiroplasma Pollmann, Marie Moore, Logan D. Krimmer, Elena D'Alvise, Paul Hasselmann, Martin Perlman, Steve J. Ballinger, Matthew J. Steidle, Johannes L.M. Gottlieb, Yuval iScience Article Cytoplasmic incompatibility (CI) is a form of reproductive manipulation caused by maternally inherited endosymbionts infecting arthropods, like Wolbachia, whereby matings between infected males and uninfected females produce few or no offspring. We report the discovery of a new CI symbiont, a strain of Spiroplasma causing CI in the parasitoid wasp Lariophagus distinguendus. Its extracellular occurrence enabled us to establish CI in uninfected adult insects by transferring Spiroplasma-infected hemolymph. We sequenced the CI-Spiroplasma genome and did not find any homologues of any of the cif genes discovered to cause CI in Wolbachia, suggesting independent evolution of CI. Instead, the genome contains other potential CI-causing candidate genes, such as homologues of high-mobility group (HMG) box proteins that are crucial in eukaryotic development but rare in bacterial genomes. Spiroplasma’s extracellular nature and broad host range encompassing medically and agriculturally important arthropods make it a promising tool to study CI and its applications. Elsevier 2022-04-29 /pmc/articles/PMC9118660/ /pubmed/35602967 http://dx.doi.org/10.1016/j.isci.2022.104335 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Pollmann, Marie Moore, Logan D. Krimmer, Elena D'Alvise, Paul Hasselmann, Martin Perlman, Steve J. Ballinger, Matthew J. Steidle, Johannes L.M. Gottlieb, Yuval Highly transmissible cytoplasmic incompatibility by the extracellular insect symbiont Spiroplasma |
title | Highly transmissible cytoplasmic incompatibility by the extracellular insect symbiont Spiroplasma |
title_full | Highly transmissible cytoplasmic incompatibility by the extracellular insect symbiont Spiroplasma |
title_fullStr | Highly transmissible cytoplasmic incompatibility by the extracellular insect symbiont Spiroplasma |
title_full_unstemmed | Highly transmissible cytoplasmic incompatibility by the extracellular insect symbiont Spiroplasma |
title_short | Highly transmissible cytoplasmic incompatibility by the extracellular insect symbiont Spiroplasma |
title_sort | highly transmissible cytoplasmic incompatibility by the extracellular insect symbiont spiroplasma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9118660/ https://www.ncbi.nlm.nih.gov/pubmed/35602967 http://dx.doi.org/10.1016/j.isci.2022.104335 |
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