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Insecticidal and Repellent Properties of Rapid-Acting Fluorine-Containing Compounds against Aedes aegypti Mosquitoes
[Image: see text] The development of safe and potent insecticides remains an integral part of a multifaceted strategy to effectively control human-disease-transmitting insect vectors. Incorporating fluorine can dramatically alter the physiochemical properties and bioavailability of insecticides. For...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10353007/ https://www.ncbi.nlm.nih.gov/pubmed/37311068 http://dx.doi.org/10.1021/acsinfecdis.3c00161 |
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author | Zhu, Xiaolong Valbon, Wilson Qiu, Mengdi Hu, Chunhua T. Yang, Jingxiang Erriah, Bryan Jankowska, Milena Dong, Ke Ward, Michael D. Kahr, Bart |
author_facet | Zhu, Xiaolong Valbon, Wilson Qiu, Mengdi Hu, Chunhua T. Yang, Jingxiang Erriah, Bryan Jankowska, Milena Dong, Ke Ward, Michael D. Kahr, Bart |
author_sort | Zhu, Xiaolong |
collection | PubMed |
description | [Image: see text] The development of safe and potent insecticides remains an integral part of a multifaceted strategy to effectively control human-disease-transmitting insect vectors. Incorporating fluorine can dramatically alter the physiochemical properties and bioavailability of insecticides. For example, 1,1,1-trichloro-2,2-bis(4-fluorophenyl)ethane (DFDT)—a difluoro congener of trichloro-2,2-bis(4-chlorophenyl)ethane (DDT)—was demonstrated previously to be 10-fold less toxic to mosquitoes than DDT in terms of LD(50) values, but it exhibited a 4-fold faster knockdown. Described herein is the discovery of fluorine-containing 1-aryl-2,2,2-trichloro-ethan-1-ols (FTEs, for fluorophenyl-trichloromethyl-ethanols). FTEs, particularly per-fluorophenyl-trichloromethyl-ethanol (PFTE), exhibited rapid knockdown not only against Drosophila melanogaster but also against susceptible and resistant Aedes aegypti mosquitoes, major vectors of Dengue, Zika, yellow fever, and Chikungunya viruses. The R enantiomer of any chiral FTE, synthesized enantioselectively, exhibited faster knockdown than its corresponding S enantiomer. PFTE does not prolong the opening of mosquito sodium channels that are characteristic of the action of DDT and pyrethroid insecticides. In addition, pyrethroid/DDT-resistant Ae. aegypti strains having enhanced P450-mediated detoxification and/or carrying sodium channel mutations that confer knockdown resistance were not cross-resistant to PFTE. These results indicate a mechanism of PFTE insecticidal action distinct from that of pyrethroids or DDT. Furthermore, PFTE elicited spatial repellency at concentrations as low as 10 ppm in a hand-in-cage assay. PFTE and MFTE were found to possess low mammalian toxicity. These results suggest the substantial potential of FTEs as a new class of compounds for controlling insect vectors, including pyrethroid/DDT-resistant mosquitoes. Further investigations of FTE insecticidal and repellency mechanisms could provide important insights into how incorporation of fluorine influences the rapid lethality and mosquito sensing. |
format | Online Article Text |
id | pubmed-10353007 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-103530072023-07-19 Insecticidal and Repellent Properties of Rapid-Acting Fluorine-Containing Compounds against Aedes aegypti Mosquitoes Zhu, Xiaolong Valbon, Wilson Qiu, Mengdi Hu, Chunhua T. Yang, Jingxiang Erriah, Bryan Jankowska, Milena Dong, Ke Ward, Michael D. Kahr, Bart ACS Infect Dis [Image: see text] The development of safe and potent insecticides remains an integral part of a multifaceted strategy to effectively control human-disease-transmitting insect vectors. Incorporating fluorine can dramatically alter the physiochemical properties and bioavailability of insecticides. For example, 1,1,1-trichloro-2,2-bis(4-fluorophenyl)ethane (DFDT)—a difluoro congener of trichloro-2,2-bis(4-chlorophenyl)ethane (DDT)—was demonstrated previously to be 10-fold less toxic to mosquitoes than DDT in terms of LD(50) values, but it exhibited a 4-fold faster knockdown. Described herein is the discovery of fluorine-containing 1-aryl-2,2,2-trichloro-ethan-1-ols (FTEs, for fluorophenyl-trichloromethyl-ethanols). FTEs, particularly per-fluorophenyl-trichloromethyl-ethanol (PFTE), exhibited rapid knockdown not only against Drosophila melanogaster but also against susceptible and resistant Aedes aegypti mosquitoes, major vectors of Dengue, Zika, yellow fever, and Chikungunya viruses. The R enantiomer of any chiral FTE, synthesized enantioselectively, exhibited faster knockdown than its corresponding S enantiomer. PFTE does not prolong the opening of mosquito sodium channels that are characteristic of the action of DDT and pyrethroid insecticides. In addition, pyrethroid/DDT-resistant Ae. aegypti strains having enhanced P450-mediated detoxification and/or carrying sodium channel mutations that confer knockdown resistance were not cross-resistant to PFTE. These results indicate a mechanism of PFTE insecticidal action distinct from that of pyrethroids or DDT. Furthermore, PFTE elicited spatial repellency at concentrations as low as 10 ppm in a hand-in-cage assay. PFTE and MFTE were found to possess low mammalian toxicity. These results suggest the substantial potential of FTEs as a new class of compounds for controlling insect vectors, including pyrethroid/DDT-resistant mosquitoes. Further investigations of FTE insecticidal and repellency mechanisms could provide important insights into how incorporation of fluorine influences the rapid lethality and mosquito sensing. American Chemical Society 2023-06-13 /pmc/articles/PMC10353007/ /pubmed/37311068 http://dx.doi.org/10.1021/acsinfecdis.3c00161 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Zhu, Xiaolong Valbon, Wilson Qiu, Mengdi Hu, Chunhua T. Yang, Jingxiang Erriah, Bryan Jankowska, Milena Dong, Ke Ward, Michael D. Kahr, Bart Insecticidal and Repellent Properties of Rapid-Acting Fluorine-Containing Compounds against Aedes aegypti Mosquitoes |
title | Insecticidal
and
Repellent Properties of Rapid-Acting
Fluorine-Containing Compounds against Aedes aegypti Mosquitoes |
title_full | Insecticidal
and
Repellent Properties of Rapid-Acting
Fluorine-Containing Compounds against Aedes aegypti Mosquitoes |
title_fullStr | Insecticidal
and
Repellent Properties of Rapid-Acting
Fluorine-Containing Compounds against Aedes aegypti Mosquitoes |
title_full_unstemmed | Insecticidal
and
Repellent Properties of Rapid-Acting
Fluorine-Containing Compounds against Aedes aegypti Mosquitoes |
title_short | Insecticidal
and
Repellent Properties of Rapid-Acting
Fluorine-Containing Compounds against Aedes aegypti Mosquitoes |
title_sort | insecticidal
and
repellent properties of rapid-acting
fluorine-containing compounds against aedes aegypti mosquitoes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10353007/ https://www.ncbi.nlm.nih.gov/pubmed/37311068 http://dx.doi.org/10.1021/acsinfecdis.3c00161 |
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