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      Anopheles gambiae larvae mount stronger immune responses against bacterial infection than adults: evidence of adaptive decoupling in mosquitoes

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          Abstract

          Background

          The immune system of adult mosquitoes has received significant attention because of the ability of females to vector disease-causing pathogens while ingesting blood meals. However, few studies have focused on the immune system of larvae, which, we hypothesize, is highly robust due to the high density and diversity of microorganisms that larvae encounter in their aquatic environments and the strong selection pressures at work in the larval stage to ensure survival to reproductive maturity. Here, we surveyed a broad range of cellular and humoral immune parameters in larvae of the malaria mosquito, Anopheles gambiae, and compared their potency to that of newly-emerged adults and older adults.

          Results

          We found that larvae kill bacteria in their hemocoel with equal or greater efficiency compared to newly-emerged adults, and that antibacterial ability declines further with adult age, indicative of senescence. This phenotype correlates with more circulating hemocytes and a differing spatial arrangement of sessile hemocytes in larvae relative to adults, as well as with the individual hemocytes of adults carrying a greater phagocytic burden. The hemolymph of larvae also possesses markedly stronger antibacterial lytic and melanization activity than the hemolymph of adults. Finally, infection induces a stronger transcriptional upregulation of immunity genes in larvae than in adults, including differences in the immunity genes that are regulated.

          Conclusions

          These results demonstrate that immunity is strongest in larvae and declines after metamorphosis and with adult age, and suggest that adaptive decoupling, or the independent evolution of larval and adult traits made possible by metamorphosis, has occurred in the mosquito lineage.

          Electronic supplementary material

          The online version of this article (doi:10.1186/s13071-017-2302-6) contains supplementary material, which is available to authorized users.

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          Most cited references132

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          For the past 25 years NIH Image and ImageJ software have been pioneers as open tools for the analysis of scientific images. We discuss the origins, challenges and solutions of these two programs, and how their history can serve to advise and inform other software projects.
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                Author and article information

                Contributors
                garrett.p.league@vanderbilt.edu
                tania.y.estevez-lao@vanderbilt.edu
                yan.yan@vanderbilt.edu
                valeriagarcia514@gmail.com
                julian.hillyer@vanderbilt.edu
                Journal
                Parasit Vectors
                Parasit Vectors
                Parasites & Vectors
                BioMed Central (London )
                1756-3305
                1 August 2017
                1 August 2017
                2017
                : 10
                : 367
                Affiliations
                ISNI 0000 0001 2264 7217, GRID grid.152326.1, Department of Biological Sciences, , Vanderbilt University, ; Nashville, TN USA
                Article
                2302
                10.1186/s13071-017-2302-6
                5539753
                28764812
                aa48adb0-3e04-47ab-b88e-d3019fa7afa5
                © The Author(s). 2017

                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
                : 9 April 2017
                : 20 July 2017
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100000060, National Institute of Allergy and Infectious Diseases;
                Award ID: R21-AI119596
                Categories
                Research
                Custom metadata
                © The Author(s) 2017

                Parasitology
                diptera,hemocyte,phagocytosis,melanization,phenoloxidase,antimicrobial peptide,hemolymph,metamorphosis

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