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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
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.
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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
title_full Genomic Insights into the Origin of Parasitism in the Emerging Plant Pathogen Bursaphelenchus xylophilus
title_fullStr Genomic Insights into the Origin of Parasitism in the Emerging Plant Pathogen Bursaphelenchus xylophilus
title_full_unstemmed Genomic Insights into the Origin of Parasitism in the Emerging Plant Pathogen Bursaphelenchus xylophilus
title_short Genomic Insights into the Origin of Parasitism in the Emerging Plant Pathogen Bursaphelenchus xylophilus
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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