Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Kim, Junheon, Lee, Sang-Myeong, Park, Chung Gyoo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
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
_version_ 1782442303215894528
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
work_keys_str_mv AT kimjunheon bursaphelenchusxylophilusiskilledbyhomologuesof21undecyloxy1ethanol
AT leesangmyeong bursaphelenchusxylophilusiskilledbyhomologuesof21undecyloxy1ethanol
AT parkchunggyoo bursaphelenchusxylophilusiskilledbyhomologuesof21undecyloxy1ethanol