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Bursaphelenchus xylophilus is killed by homologues of 2-(1-undecyloxy)-1-ethanol
2-(1-Undecyloxy)-1-ethanol, monochamol, is a male-produced aggregation pheromone of the Monochamus species, which are efficient vectors of the pine wood nematode (PWN), Bursaphelenchus xylophilus, which cause devastating damage to pines worldwide. The nematicidal activity of synthetic monochamol and...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4941398/ https://www.ncbi.nlm.nih.gov/pubmed/27403600 http://dx.doi.org/10.1038/srep29300 |
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author | Kim, Junheon Lee, Sang-Myeong Park, Chung Gyoo |
author_facet | Kim, Junheon Lee, Sang-Myeong Park, Chung Gyoo |
author_sort | Kim, Junheon |
collection | PubMed |
description | 2-(1-Undecyloxy)-1-ethanol, monochamol, is a male-produced aggregation pheromone of the Monochamus species, which are efficient vectors of the pine wood nematode (PWN), Bursaphelenchus xylophilus, which cause devastating damage to pines worldwide. The nematicidal activity of synthetic monochamol and its homologues (ROEtOH: R = C(7)-C(13)) were investigated to find potential alternatives to the currently used PWN control agents abamectin and emamectin. Compounds with C(7)-C(13) chain length alkyl groups exhibited 100% nematicidal activity at a concentration of 1000 mg/L. At a concentration of 100 mg/L, 2-(1-nonyloxy)-1-ethanol (C(9)OEtOH), 2-(1-decyloxy)-1-ethanol (C(10)OEtOH), 2-(1-undecyloxy)-1-ethanol (C(11)OEtOH), and 2-(1-dodecyloxy)-1-ethanol (C(12)OEtOH) showed 100% nematicidal activity, but the others showed weaker activities. C(11)OEtOH showed similar nematicidal activity to abamectin in terms of LD(90) values, which were 13.30 and 12.53 mg/L, respectively. However, C(9)OEtOH, C(10)OEtOH, and C(12)OEtOH (LC(90) values: 53.63, 38.18, and 46.68 mg/L, respectively) were less effective than C(11)OEtOH and abamectin. These results indicate that monochamol could be an effective alternative agent against PWN. The relationship of insecticidal and nematicidal activity to different carbon chain lengths in compounds is discussed. |
format | Online Article Text |
id | pubmed-4941398 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49413982016-07-20 Bursaphelenchus xylophilus is killed by homologues of 2-(1-undecyloxy)-1-ethanol Kim, Junheon Lee, Sang-Myeong Park, Chung Gyoo Sci Rep Article 2-(1-Undecyloxy)-1-ethanol, monochamol, is a male-produced aggregation pheromone of the Monochamus species, which are efficient vectors of the pine wood nematode (PWN), Bursaphelenchus xylophilus, which cause devastating damage to pines worldwide. The nematicidal activity of synthetic monochamol and its homologues (ROEtOH: R = C(7)-C(13)) were investigated to find potential alternatives to the currently used PWN control agents abamectin and emamectin. Compounds with C(7)-C(13) chain length alkyl groups exhibited 100% nematicidal activity at a concentration of 1000 mg/L. At a concentration of 100 mg/L, 2-(1-nonyloxy)-1-ethanol (C(9)OEtOH), 2-(1-decyloxy)-1-ethanol (C(10)OEtOH), 2-(1-undecyloxy)-1-ethanol (C(11)OEtOH), and 2-(1-dodecyloxy)-1-ethanol (C(12)OEtOH) showed 100% nematicidal activity, but the others showed weaker activities. C(11)OEtOH showed similar nematicidal activity to abamectin in terms of LD(90) values, which were 13.30 and 12.53 mg/L, respectively. However, C(9)OEtOH, C(10)OEtOH, and C(12)OEtOH (LC(90) values: 53.63, 38.18, and 46.68 mg/L, respectively) were less effective than C(11)OEtOH and abamectin. These results indicate that monochamol could be an effective alternative agent against PWN. The relationship of insecticidal and nematicidal activity to different carbon chain lengths in compounds is discussed. Nature Publishing Group 2016-07-11 /pmc/articles/PMC4941398/ /pubmed/27403600 http://dx.doi.org/10.1038/srep29300 Text en Copyright © 2016, Macmillan Publishers Limited 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 Kim, Junheon Lee, Sang-Myeong Park, Chung Gyoo Bursaphelenchus xylophilus is killed by homologues of 2-(1-undecyloxy)-1-ethanol |
title | Bursaphelenchus xylophilus is killed by homologues of 2-(1-undecyloxy)-1-ethanol |
title_full | Bursaphelenchus xylophilus is killed by homologues of 2-(1-undecyloxy)-1-ethanol |
title_fullStr | Bursaphelenchus xylophilus is killed by homologues of 2-(1-undecyloxy)-1-ethanol |
title_full_unstemmed | Bursaphelenchus xylophilus is killed by homologues of 2-(1-undecyloxy)-1-ethanol |
title_short | Bursaphelenchus xylophilus is killed by homologues of 2-(1-undecyloxy)-1-ethanol |
title_sort | bursaphelenchus xylophilus is killed by homologues of 2-(1-undecyloxy)-1-ethanol |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4941398/ https://www.ncbi.nlm.nih.gov/pubmed/27403600 http://dx.doi.org/10.1038/srep29300 |
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