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Feeding Dimorphism in a Mycophagous Nematode, Bursaphelenchus sinensis
Phenotypic plasticity has been widely reported in animals and can drive investment in new biological characters that engender ecological adaptability. The nematode family Diplogastridae, especially Pristionchus pacificus with its dramatic stomatal (feeding) dimorphism, has become an important model...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6765002/ https://www.ncbi.nlm.nih.gov/pubmed/31562356 http://dx.doi.org/10.1038/s41598-019-50462-z |
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author | Kanzaki, Natsumi Ekino, Taisuke Giblin-Davis, Robin M. |
author_facet | Kanzaki, Natsumi Ekino, Taisuke Giblin-Davis, Robin M. |
author_sort | Kanzaki, Natsumi |
collection | PubMed |
description | Phenotypic plasticity has been widely reported in animals and can drive investment in new biological characters that engender ecological adaptability. The nematode family Diplogastridae, especially Pristionchus pacificus with its dramatic stomatal (feeding) dimorphism, has become an important model system to analyze the evolutionary and developmental aspects of polyphenism. However, this plasticity has not been confirmed in other nematode groups. In the present study, we experimentally examined the feeding dimorphism of a fungal feeding free-living nematode, Bursaphelenchus sinensis. In a laboratory culturing experiment, the nematode expressed dimorphism, i.e., a small proportion of the population manifested as a predatory form. This form only occurred in females and was not clearly influenced by the presence of potential prey species. In addition, the ratio of the predatory form to the mycophagous form varied among different fungal food species grown in monoculture on different culture media. The predatory form of B. sinensis was typologically similar to the monomorphic (specialized) predators belonging to the same family. However, some essential morphological characters were slightly different from the specialized predators, and their behaviours were clearly disparate, suggesting that predation in B. sinensis is derived from a different phylogenetic origin than that of the specialized predators. |
format | Online Article Text |
id | pubmed-6765002 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67650022019-10-02 Feeding Dimorphism in a Mycophagous Nematode, Bursaphelenchus sinensis Kanzaki, Natsumi Ekino, Taisuke Giblin-Davis, Robin M. Sci Rep Article Phenotypic plasticity has been widely reported in animals and can drive investment in new biological characters that engender ecological adaptability. The nematode family Diplogastridae, especially Pristionchus pacificus with its dramatic stomatal (feeding) dimorphism, has become an important model system to analyze the evolutionary and developmental aspects of polyphenism. However, this plasticity has not been confirmed in other nematode groups. In the present study, we experimentally examined the feeding dimorphism of a fungal feeding free-living nematode, Bursaphelenchus sinensis. In a laboratory culturing experiment, the nematode expressed dimorphism, i.e., a small proportion of the population manifested as a predatory form. This form only occurred in females and was not clearly influenced by the presence of potential prey species. In addition, the ratio of the predatory form to the mycophagous form varied among different fungal food species grown in monoculture on different culture media. The predatory form of B. sinensis was typologically similar to the monomorphic (specialized) predators belonging to the same family. However, some essential morphological characters were slightly different from the specialized predators, and their behaviours were clearly disparate, suggesting that predation in B. sinensis is derived from a different phylogenetic origin than that of the specialized predators. Nature Publishing Group UK 2019-09-27 /pmc/articles/PMC6765002/ /pubmed/31562356 http://dx.doi.org/10.1038/s41598-019-50462-z Text en © The Author(s) 2019 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 Kanzaki, Natsumi Ekino, Taisuke Giblin-Davis, Robin M. Feeding Dimorphism in a Mycophagous Nematode, Bursaphelenchus sinensis |
title | Feeding Dimorphism in a Mycophagous Nematode, Bursaphelenchus sinensis |
title_full | Feeding Dimorphism in a Mycophagous Nematode, Bursaphelenchus sinensis |
title_fullStr | Feeding Dimorphism in a Mycophagous Nematode, Bursaphelenchus sinensis |
title_full_unstemmed | Feeding Dimorphism in a Mycophagous Nematode, Bursaphelenchus sinensis |
title_short | Feeding Dimorphism in a Mycophagous Nematode, Bursaphelenchus sinensis |
title_sort | feeding dimorphism in a mycophagous nematode, bursaphelenchus sinensis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6765002/ https://www.ncbi.nlm.nih.gov/pubmed/31562356 http://dx.doi.org/10.1038/s41598-019-50462-z |
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