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Ultrastructural plasticity in the plant-parasitic nematode, Bursaphelenchus xylophilus
Phenotypic plasticity is one of the most important strategies used by organisms with low mobility to survive in fluctuating environments. Phenotypic plasticity plays a vital role in nematodes because they have small bodies and lack wings or legs and thus, cannot move far by themselves. Bursaphelench...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7360551/ https://www.ncbi.nlm.nih.gov/pubmed/32665657 http://dx.doi.org/10.1038/s41598-020-68503-3 |
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author | Ekino, Taisuke Kirino, Haru Kanzaki, Natsumi Shinya, Ryoji |
author_facet | Ekino, Taisuke Kirino, Haru Kanzaki, Natsumi Shinya, Ryoji |
author_sort | Ekino, Taisuke |
collection | PubMed |
description | Phenotypic plasticity is one of the most important strategies used by organisms with low mobility to survive in fluctuating environments. Phenotypic plasticity plays a vital role in nematodes because they have small bodies and lack wings or legs and thus, cannot move far by themselves. Bursaphelenchus xylophilus, the pathogenic nematode species that causes pine wilt disease, experiences fluctuating conditions throughout their life history; i.e., in both the phytophagous and mycetophagous phases. However, whether the functional morphology changes between the life phases of B. xylophilus remains unknown. Our study revealed differences in the ultrastructure of B. xylophilus between the two phases. Well-developed lateral alae and atrophied intestinal microvilli were observed in the phytophagous phase compared with the mycetophagous phase. The ultrastructure in the phytophagous phase was morphologically similar to that at the dauer stage, which enables the larvae to survive in harsh environments. It suggests that the living tree represents a harsh environment for B. xylophilus, and ultrastructural phenotypic plasticity is a key strategy for B. xylophilus to survive in a living tree. In addition, ultrastructural observations of obligate plant-parasitic species closely related to B. xylophilus revealed that B. xylophilus may be in the process of adapting to feed on plant cells. |
format | Online Article Text |
id | pubmed-7360551 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73605512020-07-16 Ultrastructural plasticity in the plant-parasitic nematode, Bursaphelenchus xylophilus Ekino, Taisuke Kirino, Haru Kanzaki, Natsumi Shinya, Ryoji Sci Rep Article Phenotypic plasticity is one of the most important strategies used by organisms with low mobility to survive in fluctuating environments. Phenotypic plasticity plays a vital role in nematodes because they have small bodies and lack wings or legs and thus, cannot move far by themselves. Bursaphelenchus xylophilus, the pathogenic nematode species that causes pine wilt disease, experiences fluctuating conditions throughout their life history; i.e., in both the phytophagous and mycetophagous phases. However, whether the functional morphology changes between the life phases of B. xylophilus remains unknown. Our study revealed differences in the ultrastructure of B. xylophilus between the two phases. Well-developed lateral alae and atrophied intestinal microvilli were observed in the phytophagous phase compared with the mycetophagous phase. The ultrastructure in the phytophagous phase was morphologically similar to that at the dauer stage, which enables the larvae to survive in harsh environments. It suggests that the living tree represents a harsh environment for B. xylophilus, and ultrastructural phenotypic plasticity is a key strategy for B. xylophilus to survive in a living tree. In addition, ultrastructural observations of obligate plant-parasitic species closely related to B. xylophilus revealed that B. xylophilus may be in the process of adapting to feed on plant cells. Nature Publishing Group UK 2020-07-14 /pmc/articles/PMC7360551/ /pubmed/32665657 http://dx.doi.org/10.1038/s41598-020-68503-3 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Ekino, Taisuke Kirino, Haru Kanzaki, Natsumi Shinya, Ryoji Ultrastructural plasticity in the plant-parasitic nematode, Bursaphelenchus xylophilus |
title | Ultrastructural plasticity in the plant-parasitic nematode, Bursaphelenchus xylophilus |
title_full | Ultrastructural plasticity in the plant-parasitic nematode, Bursaphelenchus xylophilus |
title_fullStr | Ultrastructural plasticity in the plant-parasitic nematode, Bursaphelenchus xylophilus |
title_full_unstemmed | Ultrastructural plasticity in the plant-parasitic nematode, Bursaphelenchus xylophilus |
title_short | Ultrastructural plasticity in the plant-parasitic nematode, Bursaphelenchus xylophilus |
title_sort | ultrastructural plasticity in the plant-parasitic nematode, bursaphelenchus xylophilus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7360551/ https://www.ncbi.nlm.nih.gov/pubmed/32665657 http://dx.doi.org/10.1038/s41598-020-68503-3 |
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