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Genomic evidence for plant-parasitic nematodes as the earliest Wolbachia hosts
Wolbachia, one of the most widespread endosymbionts, is a target for biological control of mosquito-borne diseases (malaria and dengue virus), and antibiotic elimination of infectious filarial nematodes. We sequenced and analyzed the genome of a new Wolbachia strain (wPpe) in the plant-parasitic nem...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5062116/ https://www.ncbi.nlm.nih.gov/pubmed/27734894 http://dx.doi.org/10.1038/srep34955 |
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author | Brown, Amanda M. V. Wasala, Sulochana K. Howe, Dana K. Peetz, Amy B. Zasada, Inga A. Denver, Dee R. |
author_facet | Brown, Amanda M. V. Wasala, Sulochana K. Howe, Dana K. Peetz, Amy B. Zasada, Inga A. Denver, Dee R. |
author_sort | Brown, Amanda M. V. |
collection | PubMed |
description | Wolbachia, one of the most widespread endosymbionts, is a target for biological control of mosquito-borne diseases (malaria and dengue virus), and antibiotic elimination of infectious filarial nematodes. We sequenced and analyzed the genome of a new Wolbachia strain (wPpe) in the plant-parasitic nematode Pratylenchus penetrans. Phylogenomic analyses placed wPpe as the earliest diverging Wolbachia, suggesting two evolutionary invasions into nematodes. The next branches comprised strains in sap-feeding insects, suggesting Wolbachia may have first evolved as a nutritional mutualist. Genome size, protein content, %GC, and repetitive DNA allied wPpe with mutualistic Wolbachia, whereas gene repertoire analyses placed it between parasite (A, B) and mutualist (C, D, F) groups. Conservation of iron metabolism genes across Wolbachia suggests iron homeostasis as a potential factor in its success. This study enhances our understanding of this globally pandemic endosymbiont, highlighting genetic patterns associated with host changes. Combined with future work on this strain, these genomic data could help provide potential new targets for plant-parasitic nematode control. |
format | Online Article Text |
id | pubmed-5062116 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50621162016-10-24 Genomic evidence for plant-parasitic nematodes as the earliest Wolbachia hosts Brown, Amanda M. V. Wasala, Sulochana K. Howe, Dana K. Peetz, Amy B. Zasada, Inga A. Denver, Dee R. Sci Rep Article Wolbachia, one of the most widespread endosymbionts, is a target for biological control of mosquito-borne diseases (malaria and dengue virus), and antibiotic elimination of infectious filarial nematodes. We sequenced and analyzed the genome of a new Wolbachia strain (wPpe) in the plant-parasitic nematode Pratylenchus penetrans. Phylogenomic analyses placed wPpe as the earliest diverging Wolbachia, suggesting two evolutionary invasions into nematodes. The next branches comprised strains in sap-feeding insects, suggesting Wolbachia may have first evolved as a nutritional mutualist. Genome size, protein content, %GC, and repetitive DNA allied wPpe with mutualistic Wolbachia, whereas gene repertoire analyses placed it between parasite (A, B) and mutualist (C, D, F) groups. Conservation of iron metabolism genes across Wolbachia suggests iron homeostasis as a potential factor in its success. This study enhances our understanding of this globally pandemic endosymbiont, highlighting genetic patterns associated with host changes. Combined with future work on this strain, these genomic data could help provide potential new targets for plant-parasitic nematode control. Nature Publishing Group 2016-10-13 /pmc/articles/PMC5062116/ /pubmed/27734894 http://dx.doi.org/10.1038/srep34955 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Brown, Amanda M. V. Wasala, Sulochana K. Howe, Dana K. Peetz, Amy B. Zasada, Inga A. Denver, Dee R. Genomic evidence for plant-parasitic nematodes as the earliest Wolbachia hosts |
title | Genomic evidence for plant-parasitic nematodes as the earliest Wolbachia hosts |
title_full | Genomic evidence for plant-parasitic nematodes as the earliest Wolbachia hosts |
title_fullStr | Genomic evidence for plant-parasitic nematodes as the earliest Wolbachia hosts |
title_full_unstemmed | Genomic evidence for plant-parasitic nematodes as the earliest Wolbachia hosts |
title_short | Genomic evidence for plant-parasitic nematodes as the earliest Wolbachia hosts |
title_sort | genomic evidence for plant-parasitic nematodes as the earliest wolbachia hosts |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5062116/ https://www.ncbi.nlm.nih.gov/pubmed/27734894 http://dx.doi.org/10.1038/srep34955 |
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