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Evaluation of benzaldehyde derivatives from Morinda officinalis as anti-mite agents with dual function as acaricide and mite indicator

Severe fever with thrombocytopenia syndrome (SFTS) is an emerging infectious disease caused by SFTS virus with 12–30% fatality rate. Despite severity of the disease, any medication or treatment for SFTS has not developed yet. One approach to prevent SFTS spreading is to control the arthropod vector...

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Autores principales: Yang, Ji-Yeon, Kim, Min-Gi, Park, Jun-Hwan, Hong, Seong-Tshool, Lee, Hoi-Seon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4248270/
https://www.ncbi.nlm.nih.gov/pubmed/25434408
http://dx.doi.org/10.1038/srep07149
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author Yang, Ji-Yeon
Kim, Min-Gi
Park, Jun-Hwan
Hong, Seong-Tshool
Lee, Hoi-Seon
author_facet Yang, Ji-Yeon
Kim, Min-Gi
Park, Jun-Hwan
Hong, Seong-Tshool
Lee, Hoi-Seon
author_sort Yang, Ji-Yeon
collection PubMed
description Severe fever with thrombocytopenia syndrome (SFTS) is an emerging infectious disease caused by SFTS virus with 12–30% fatality rate. Despite severity of the disease, any medication or treatment for SFTS has not developed yet. One approach to prevent SFTS spreading is to control the arthropod vector carrying SFTS virus. We report that 2–methylbenzaldehyde analogues from M. officinalis have a dual function as acaricide against Dermatophagoides spp. and Haemaphysalis longicornis and indicator (color change) against Dermatophagoides spp. Based on the LD(50) values, 2,4,5–trimethylbenzaldehyde (0.21, 0.19, and 0.68 μg/cm(3)) had the highest fumigant activity against D. farinae, D. pteronyssinus, and H. longicornis, followed by 2,3–dimethylbenzaldehyde (0.46, 0.44, and 0.79 μg/cm(3)), 2,4–dimethylbenzaldehyde (0.66, 0.59, and 0.95 μg/cm(3)), 2,5–dimethylbenzaldehyde (0.65, 0.68, and 0.88 μg/cm(3)), 2–methylbenzaldehyde (0.95, 0.87, and 1.28 μg/cm(3)), 3–methylbenzaldehyde (0.99, 0.93, and 1.38 μg/cm(3)), 4–methylbenzaldehyde (1.17, 1.15, and 3.67 μg/cm(3)), and M. officinalis oil (7.05, 7.00, and 19.70 μg/cm(3)). Furthermore, color alteration of Dermatophagoides spp. was shown to be induced, from colorless to dark brown, by the treatment of 2,3–dihydroxybenzaldehyde. These finding indicated that 2–methylbenzaldehyde analogues could be developed as functional agent associated with the arthropod vector of SFTS virus and allergen.
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spelling pubmed-42482702014-12-08 Evaluation of benzaldehyde derivatives from Morinda officinalis as anti-mite agents with dual function as acaricide and mite indicator Yang, Ji-Yeon Kim, Min-Gi Park, Jun-Hwan Hong, Seong-Tshool Lee, Hoi-Seon Sci Rep Article Severe fever with thrombocytopenia syndrome (SFTS) is an emerging infectious disease caused by SFTS virus with 12–30% fatality rate. Despite severity of the disease, any medication or treatment for SFTS has not developed yet. One approach to prevent SFTS spreading is to control the arthropod vector carrying SFTS virus. We report that 2–methylbenzaldehyde analogues from M. officinalis have a dual function as acaricide against Dermatophagoides spp. and Haemaphysalis longicornis and indicator (color change) against Dermatophagoides spp. Based on the LD(50) values, 2,4,5–trimethylbenzaldehyde (0.21, 0.19, and 0.68 μg/cm(3)) had the highest fumigant activity against D. farinae, D. pteronyssinus, and H. longicornis, followed by 2,3–dimethylbenzaldehyde (0.46, 0.44, and 0.79 μg/cm(3)), 2,4–dimethylbenzaldehyde (0.66, 0.59, and 0.95 μg/cm(3)), 2,5–dimethylbenzaldehyde (0.65, 0.68, and 0.88 μg/cm(3)), 2–methylbenzaldehyde (0.95, 0.87, and 1.28 μg/cm(3)), 3–methylbenzaldehyde (0.99, 0.93, and 1.38 μg/cm(3)), 4–methylbenzaldehyde (1.17, 1.15, and 3.67 μg/cm(3)), and M. officinalis oil (7.05, 7.00, and 19.70 μg/cm(3)). Furthermore, color alteration of Dermatophagoides spp. was shown to be induced, from colorless to dark brown, by the treatment of 2,3–dihydroxybenzaldehyde. These finding indicated that 2–methylbenzaldehyde analogues could be developed as functional agent associated with the arthropod vector of SFTS virus and allergen. Nature Publishing Group 2014-12-01 /pmc/articles/PMC4248270/ /pubmed/25434408 http://dx.doi.org/10.1038/srep07149 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 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 in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Article
Yang, Ji-Yeon
Kim, Min-Gi
Park, Jun-Hwan
Hong, Seong-Tshool
Lee, Hoi-Seon
Evaluation of benzaldehyde derivatives from Morinda officinalis as anti-mite agents with dual function as acaricide and mite indicator
title Evaluation of benzaldehyde derivatives from Morinda officinalis as anti-mite agents with dual function as acaricide and mite indicator
title_full Evaluation of benzaldehyde derivatives from Morinda officinalis as anti-mite agents with dual function as acaricide and mite indicator
title_fullStr Evaluation of benzaldehyde derivatives from Morinda officinalis as anti-mite agents with dual function as acaricide and mite indicator
title_full_unstemmed Evaluation of benzaldehyde derivatives from Morinda officinalis as anti-mite agents with dual function as acaricide and mite indicator
title_short Evaluation of benzaldehyde derivatives from Morinda officinalis as anti-mite agents with dual function as acaricide and mite indicator
title_sort evaluation of benzaldehyde derivatives from morinda officinalis as anti-mite agents with dual function as acaricide and mite indicator
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4248270/
https://www.ncbi.nlm.nih.gov/pubmed/25434408
http://dx.doi.org/10.1038/srep07149
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