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      Synergy in the adulticidal efficacy of essential oils for the improvement of permethrin toxicity against Aedes aegypti L. (Diptera: Culicidae)

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          Abstract

          Background

          In a previous screening program for mosquitocides from local edible plants in Thailand, essential oils (EOs) of Cyperus rotundus, Alpinia galanga and Cinnamomum verum, were found to possess promising adulticidal activity against Aedes aegypti. With the aim of reducing usage of conventional insecticides and improving the management of resistant mosquito populations, this study was designed to determine the potential synergism in the adulticidal efficacy of EOs on permethrin toxicity against Ae. aegypti, both pyrethroid-resistant and -susceptible strains .

          Methods

          EOs extracted from rhizomes of C. rotundus and A. galanga as well as C. verum barks were evaluated for chemical compositions and adulticidal activity against Muang Chiang Mai-susceptible (MCM-S) and Pang Mai Dang-resistant (PMD-R) strains of Ae. aegypti. Adulticidal bioassays of EO-permethrin mixtures for synergistic activity were also performed on these Ae. aegypti strains.

          Results

          Chemical characterization by the GC-MS analytical technique demonstrated that 48 compounds were identified from the EOs of C. rotundus, A. galanga and C. verum, representing 80.22%, 86.75% and 97.24%, respectively, of all compositions. Cyperene (14.04%), β-bisabolene (18.27%) and cinnamaldehyde (64.66%) were the main constituents of C. rotundus, A. galanga and C. verum oils, respectively. In adulticidal bioassays, EOs of C. rotundus, A. galanga and C. verum were effective in killing Ae. aegypti, both MCM-S and PMD-R strains, with LD 50 values of 10.05 and 9.57 μg/mg female, 7.97 and 7.94 μg/mg female, and 3.30 and 3.22 μg/mg female, respectively. The adulticidal efficacy against MCM-S and PMD-R Ae. aegypti of these EOs was close to that of piperonyl butoxide (PBO, LD 50 values = 6.30 and 4.79 μg/mg female, respectively) but less pronounced than that of permethrin (LD 50 values = 0.44 and 3.70 ng/mg female, respectively). Nevertheless, combination-based bioassays discovered the accomplished synergism of EOs together with permethrin. Significant synergistic effects with permethrin against both the strains of Ae. aegypti were recorded in the EOs of C. rotundus and A. galanga. Addition of C. rotundus and A. galanga oils decreased the LD 50 values of permethrin against MCM-S dramatically from 0.44 to 0.07 and 0.11 ng/mg female, respectively, with synergism ratio (SR) values of 6.28 and 4.00, respectively. Furthermore, EOs of C. rotundus and A. galanga also reduced the LD 50 values of permethrin against PMD-R drastically from 3.70 to 0.42 and 0.003 ng/mg female, respectively, with SR values of 8.81 and 1233.33, respectively.

          Conclusions

          The synergy of enhanced adulticidal toxicity recorded from EO-permethrin combinations against both strains of Ae. aegypti presents a promising role of EOs as a synergist for improving mosquitocidal efficacy, particularly in situations where conventional compounds are ineffective or inappropriate.

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          Botanical insecticides, deterrents, and repellents in modern agriculture and an increasingly regulated world.

          Botanical insecticides have long been touted as attractive alternatives to synthetic chemical insecticides for pest management because botanicals reputedly pose little threat to the environment or to human health. The body of scientific literature documenting bioactivity of plant derivatives to arthropod pests continues to expand, yet only a handful of botanicals are currently used in agriculture in the industrialized world, and there are few prospects for commercial development of new botanical products. Pyrethrum and neem are well established commercially, pesticides based on plant essential oils have recently entered the marketplace, and the use of rotenone appears to be waning. A number of plant substances have been considered for use as insect antifeedants or repellents, but apart from some natural mosquito repellents, little commercial success has ensued for plant substances that modify arthropod behavior. Several factors appear to limit the success of botanicals, most notably regulatory barriers and the availability of competing products (newer synthetics, fermentation products, microbials) that are cost-effective and relatively safe compared with their predecessors. In the context of agricultural pest management, botanical insecticides are best suited for use in organic food production in industrialized countries but can play a much greater role in the production and postharvest protection of food in developing countries.
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            Defining Challenges and Proposing Solutions for Control of the Virus Vector Aedes aegypti

            If done properly, say the authors,Aedes aegypti suppression is a practical method to control urban dengue, yellow fever, and chikungunya viruses.
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              Insecticide resistance in the major dengue vectors Aedes albopictus and Aedes aegypti

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                Author and article information

                Contributors
                ar.chansang@gmail.com
                ruda_0@hotmail.com
                anuluck.j@cmu.ac.th
                ajitpakdi2@yahoo.com
                doung_prim@yahoo.com
                arunee.k@mju.ac.th
                doungrat.riyong@cmu.ac.th
                anchalee.wa@cmu.ac.th
                tangmo.parasite@gmail.com
                belle_roong@hotmail.com
                benjawan.p@cmu.ac.th
                Journal
                Parasit Vectors
                Parasit Vectors
                Parasites & Vectors
                BioMed Central (London )
                1756-3305
                13 July 2018
                13 July 2018
                2018
                : 11
                : 417
                Affiliations
                [1 ]ISNI 0000 0000 9039 7662, GRID grid.7132.7, Center of Insect Vector Study, Department of Parasitology, Faculty of Medicine, , Chiang Mai University, ; Chiang Mai, 50200 Thailand
                [2 ]ISNI 0000 0000 9039 7662, GRID grid.7132.7, Graduate PhD’s Degree Program in Parasitology, Faculty of Medicine, , Chiang Mai University, ; Chiang Mai, 50200 Thailand
                [3 ]ISNI 0000 0000 9291 0538, GRID grid.411558.c, Faculty of Fisheries Technology and Aquatic Resources, , Maejo University, ; Chiang Mai, 50290 Thailand
                [4 ]ISNI 0000 0000 9291 0538, GRID grid.411558.c, Program in Chemistry, Faculty of Science, , Maejo University, ; Chiang Mai, 50290 Thailand
                Article
                3001
                10.1186/s13071-018-3001-7
                6045857
                30005688
                16ca9e9b-08eb-4bad-9ebb-d628de7be504
                © The Author(s). 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 20 May 2018
                : 6 July 2018
                Funding
                Funded by: the Faculty of Medicine Research Fund, CMU
                Funded by: Diamond Research Grant of the Faculty of Medicine, CMU
                Funded by: the Excellence Center in Insect Vector Study of the research administration, CMU
                Categories
                Research
                Custom metadata
                © The Author(s) 2018

                Parasitology
                aedes aegypti,cyperus rotundus,alpinia galanga,cinnamomum verum,synergy,adulticidal,essential oils,permethrin

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