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      Resistance to the larvicide temephos and altered egg and larval surfaces characterize salinity-tolerant Aedes aegypti

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          Abstract

          Aedes aegypti, the principal global vector of arboviral diseases and previously considered to oviposit and undergo preimaginal development only in fresh water, has recently been shown to be capable of developing in coastal brackish water containing up to 15 g/L salt. We investigated surface changes in eggs and larval cuticles by atomic force and scanning electron microscopy, and larval susceptibility to two widely-used larvicides, temephos and Bacillus thuringiensis, in brackish water-adapted Ae. aegypti. Compared to freshwater forms, salinity-tolerant Ae. aegypti had rougher and less elastic egg surfaces, eggs that hatched better in brackish water, rougher larval cuticle surfaces, and larvae more resistant to the organophosphate insecticide temephos . Larval cuticle and egg surface changes in salinity-tolerant Ae. aegypti are proposed to respectively contribute to the increased temephos resistance and egg hatchability in brackish water. The findings highlight the importance of extending Aedes vector larval source reduction efforts to brackish water habitats and monitoring the efficacy of larvicides in coastal areas worldwide.

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          Gwyddion: an open-source software for SPM data analysis

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            The molecular basis of insecticide resistance in mosquitoes.

            Insecticide resistance is an inherited characteristic involving changes in one or more insect gene. The molecular basis of these changes are only now being fully determined, aided by the availability of the Drosophila melanogaster and Anopheles gambiae genome sequences. This paper reviews what is currently known about insecticide resistance conferred by metabolic or target site changes in mosquitoes.
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              Dispersal of the dengue vector Aedes aegypti within and between rural communities.

              Knowledge of mosquito dispersal is critical for vector-borne disease control and prevention strategies and for understanding population structure and pathogen dissemination. We determined Aedes aegypti flight range and dispersal patterns from 21 mark-release-recapture experiments conducted over 11 years (1991-2002) in Puerto Rico and Thailand. Dispersal was compared by release location, sex, age, season, and village. For all experiments, the majority of mosquitoes were collected from their release house or adjacent house. Inter-village movement was detected rarely, with a few mosquitoes moving a maximum of 512 meters from one Thai village to the next. Average dispersal distances were similar for males and females and females released indoors versus outdoors. The movement of Ae. aegypti was not influenced by season or age, but differed by village. Results demonstrate that adult Ae. aegypti disperse relatively short distances, suggesting that people rather than mosquitoes are the primary mode of dengue virus dissemination within and among communities.
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                Author and article information

                Contributors
                rjr200911@yahoo.com
                noble@univ.jfn.ac.lk
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                19 May 2023
                19 May 2023
                2023
                : 13
                : 8160
                Affiliations
                [1 ]GRID grid.412985.3, ISNI 0000 0001 0156 4834, Department of Zoology, Faculty of Science, , University of Jaffna, ; Jaffna, 40000 Sri Lanka
                [2 ]GRID grid.412985.3, ISNI 0000 0001 0156 4834, Department of Physics, Faculty of Science, , University of Jaffna, ; Jaffna, 40000 Sri Lanka
                [3 ]GRID grid.5734.5, ISNI 0000 0001 0726 5157, Department of Infectious Diseases and Pathobiology, Vetsuisse Faculty, Institute of Parasitology, , University of Bern, ; Länggass-Strasse 122, 3012 Bern, Switzerland
                Author information
                http://orcid.org/0000-0003-0246-7053
                http://orcid.org/0000-0002-7861-2037
                Article
                35128
                10.1038/s41598-023-35128-1
                10198600
                b424d914-aac8-4240-8d77-578e28c4b203
                © The Author(s) 2023

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 8 December 2022
                : 12 May 2023
                Funding
                Funded by: Switzerland National Science Foundation through its Programme for International Research by Scientific Investigation Teams
                Award ID: IZSTZO: 191762
                Categories
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                © Springer Nature Limited 2023

                Uncategorized
                ecology,zoology
                Uncategorized
                ecology, zoology

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