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Genomic Insights into the Origin of Parasitism in the Emerging Plant Pathogen Bursaphelenchus xylophilus
Bursaphelenchus xylophilus is the nematode responsible for a devastating epidemic of pine wilt disease in Asia and Europe, and represents a recent, independent origin of plant parasitism in nematodes, ecologically and taxonomically distinct from other nematodes for which genomic data is available. A...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3164644/ https://www.ncbi.nlm.nih.gov/pubmed/21909270 http://dx.doi.org/10.1371/journal.ppat.1002219 |
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author | Kikuchi, Taisei Cotton, James A. Dalzell, Jonathan J. Hasegawa, Koichi Kanzaki, Natsumi McVeigh, Paul Takanashi, Takuma Tsai, Isheng J. Assefa, Samuel A. Cock, Peter J. A. Otto, Thomas Dan Hunt, Martin Reid, Adam J. Sanchez-Flores, Alejandro Tsuchihara, Kazuko Yokoi, Toshiro Larsson, Mattias C. Miwa, Johji Maule, Aaron G. Sahashi, Norio Jones, John T. Berriman, Matthew |
author_facet | Kikuchi, Taisei Cotton, James A. Dalzell, Jonathan J. Hasegawa, Koichi Kanzaki, Natsumi McVeigh, Paul Takanashi, Takuma Tsai, Isheng J. Assefa, Samuel A. Cock, Peter J. A. Otto, Thomas Dan Hunt, Martin Reid, Adam J. Sanchez-Flores, Alejandro Tsuchihara, Kazuko Yokoi, Toshiro Larsson, Mattias C. Miwa, Johji Maule, Aaron G. Sahashi, Norio Jones, John T. Berriman, Matthew |
author_sort | Kikuchi, Taisei |
collection | PubMed |
description | Bursaphelenchus xylophilus is the nematode responsible for a devastating epidemic of pine wilt disease in Asia and Europe, and represents a recent, independent origin of plant parasitism in nematodes, ecologically and taxonomically distinct from other nematodes for which genomic data is available. As well as being an important pathogen, the B. xylophilus genome thus provides a unique opportunity to study the evolution and mechanism of plant parasitism. Here, we present a high-quality draft genome sequence from an inbred line of B. xylophilus, and use this to investigate the biological basis of its complex ecology which combines fungal feeding, plant parasitic and insect-associated stages. We focus particularly on putative parasitism genes as well as those linked to other key biological processes and demonstrate that B. xylophilus is well endowed with RNA interference effectors, peptidergic neurotransmitters (including the first description of ins genes in a parasite) stress response and developmental genes and has a contracted set of chemosensory receptors. B. xylophilus has the largest number of digestive proteases known for any nematode and displays expanded families of lysosome pathway genes, ABC transporters and cytochrome P450 pathway genes. This expansion in digestive and detoxification proteins may reflect the unusual diversity in foods it exploits and environments it encounters during its life cycle. In addition, B. xylophilus possesses a unique complement of plant cell wall modifying proteins acquired by horizontal gene transfer, underscoring the impact of this process on the evolution of plant parasitism by nematodes. Together with the lack of proteins homologous to effectors from other plant parasitic nematodes, this confirms the distinctive molecular basis of plant parasitism in the Bursaphelenchus lineage. The genome sequence of B. xylophilus adds to the diversity of genomic data for nematodes, and will be an important resource in understanding the biology of this unusual parasite. |
format | Online Article Text |
id | pubmed-3164644 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-31646442011-09-09 Genomic Insights into the Origin of Parasitism in the Emerging Plant Pathogen Bursaphelenchus xylophilus Kikuchi, Taisei Cotton, James A. Dalzell, Jonathan J. Hasegawa, Koichi Kanzaki, Natsumi McVeigh, Paul Takanashi, Takuma Tsai, Isheng J. Assefa, Samuel A. Cock, Peter J. A. Otto, Thomas Dan Hunt, Martin Reid, Adam J. Sanchez-Flores, Alejandro Tsuchihara, Kazuko Yokoi, Toshiro Larsson, Mattias C. Miwa, Johji Maule, Aaron G. Sahashi, Norio Jones, John T. Berriman, Matthew PLoS Pathog Research Article Bursaphelenchus xylophilus is the nematode responsible for a devastating epidemic of pine wilt disease in Asia and Europe, and represents a recent, independent origin of plant parasitism in nematodes, ecologically and taxonomically distinct from other nematodes for which genomic data is available. As well as being an important pathogen, the B. xylophilus genome thus provides a unique opportunity to study the evolution and mechanism of plant parasitism. Here, we present a high-quality draft genome sequence from an inbred line of B. xylophilus, and use this to investigate the biological basis of its complex ecology which combines fungal feeding, plant parasitic and insect-associated stages. We focus particularly on putative parasitism genes as well as those linked to other key biological processes and demonstrate that B. xylophilus is well endowed with RNA interference effectors, peptidergic neurotransmitters (including the first description of ins genes in a parasite) stress response and developmental genes and has a contracted set of chemosensory receptors. B. xylophilus has the largest number of digestive proteases known for any nematode and displays expanded families of lysosome pathway genes, ABC transporters and cytochrome P450 pathway genes. This expansion in digestive and detoxification proteins may reflect the unusual diversity in foods it exploits and environments it encounters during its life cycle. In addition, B. xylophilus possesses a unique complement of plant cell wall modifying proteins acquired by horizontal gene transfer, underscoring the impact of this process on the evolution of plant parasitism by nematodes. Together with the lack of proteins homologous to effectors from other plant parasitic nematodes, this confirms the distinctive molecular basis of plant parasitism in the Bursaphelenchus lineage. The genome sequence of B. xylophilus adds to the diversity of genomic data for nematodes, and will be an important resource in understanding the biology of this unusual parasite. Public Library of Science 2011-09-01 /pmc/articles/PMC3164644/ /pubmed/21909270 http://dx.doi.org/10.1371/journal.ppat.1002219 Text en Kikuchi et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Kikuchi, Taisei Cotton, James A. Dalzell, Jonathan J. Hasegawa, Koichi Kanzaki, Natsumi McVeigh, Paul Takanashi, Takuma Tsai, Isheng J. Assefa, Samuel A. Cock, Peter J. A. Otto, Thomas Dan Hunt, Martin Reid, Adam J. Sanchez-Flores, Alejandro Tsuchihara, Kazuko Yokoi, Toshiro Larsson, Mattias C. Miwa, Johji Maule, Aaron G. Sahashi, Norio Jones, John T. Berriman, Matthew Genomic Insights into the Origin of Parasitism in the Emerging Plant Pathogen Bursaphelenchus xylophilus |
title | Genomic Insights into the Origin of Parasitism in the Emerging Plant Pathogen Bursaphelenchus xylophilus
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title_full | Genomic Insights into the Origin of Parasitism in the Emerging Plant Pathogen Bursaphelenchus xylophilus
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title_fullStr | Genomic Insights into the Origin of Parasitism in the Emerging Plant Pathogen Bursaphelenchus xylophilus
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title_full_unstemmed | Genomic Insights into the Origin of Parasitism in the Emerging Plant Pathogen Bursaphelenchus xylophilus
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title_short | Genomic Insights into the Origin of Parasitism in the Emerging Plant Pathogen Bursaphelenchus xylophilus
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title_sort | genomic insights into the origin of parasitism in the emerging plant pathogen bursaphelenchus xylophilus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3164644/ https://www.ncbi.nlm.nih.gov/pubmed/21909270 http://dx.doi.org/10.1371/journal.ppat.1002219 |
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