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      Diet modulates the relationship between immune gene expression and functional immune responses

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          Abstract

          Nutrition is vital to health and the availability of resources has long been acknowledged as a key factor in the ability to fight off parasites, as investing in the immune system is costly. Resources have typically been considered as something of a “black box”, with the quantity of available food being used as a proxy for resource limitation. However, food is a complex mixture of macro- and micronutrients, the precise balance of which determines an animal's fitness. Here we use a state-space modelling approach, the Geometric Framework for Nutrition (GFN), to assess for the first time, how the balance and amount of nutrients affects an animal's ability to mount an immune response to a pathogenic infection.

          Spodoptera littoralis caterpillars were assigned to one of 20 diets that varied in the ratio of macronutrients (protein and carbohydrate) and their calorie content to cover a large region of nutrient space. Caterpillars were then handled or injected with either live or dead Xenorhabdus nematophila bacterial cells. The expression of nine genes (5 immune, 4 non-immune) was measured 20 h post immune challenge. For two of the immune genes (PPO and Lysozyme) we also measured the relevant functional immune response in the hemolymph. Gene expression and functional immune responses were then mapped against nutritional intake.

          The expression of all immune genes was up-regulated by injection with dead bacteria, but only those in the IMD pathway (Moricin and Relish) were substantially up-regulated by both dead and live bacterial challenge. Functional immune responses increased with the protein content of the diet but the expression of immune genes was much less predictable.

          Our results indicate that diet does play an important role in the ability of an animal to mount an adequate immune response, with the availability of protein being the most important predictor of the functional (physiological) immune response. Importantly, however, immune gene expression responds quite differently to functional immunity and we would caution against using gene expression as a proxy for immune investment, as it is unlikely to be reliable indicator of the immune response, except under specific dietary conditions.

          Graphical abstract

          Highlights

          • High protein diets improved survival after live bacterial infection.

          • Injection with dead bacteria increased expression of Toll and IMD immune genes.

          • Injection with live bacteria inhibited immune gene expression (GE).

          • The ratio and concentration of macronutrients in the diet affected GE.

          • GE only predicted functional immune activity at high levels of dietary protein.

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          Most cited references54

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          Survival for immunity: the price of immune system activation for bumblebee workers.

          Parasites do not always harm their hosts because the immune system keeps an infection at bay. Ironically, the cost of using immune defenses could itself reduce host fitness. This indirect cost of parasitism is often not visible because of compensatory resource intake. Here, workers of the bumblebee, Bombus terrestris, were challenged with lipopolysaccharides and micro-latex beads to induce their immune system under starvation (i.e., not allowing compensatory intake). Compared with controls, survival of induced workers was significantly reduced (by 50 to 70%).
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            Sex-specific fitness effects of nutrient intake on reproduction and lifespan.

            Diet affects both lifespan and reproduction [1-9], leading to the prediction that the contrasting reproductive strategies of the sexes should result in sex-specific effects of nutrition on fitness and longevity [6, 10] and favor different patterns of nutrient intake in males and females. However, males and females share most of their genome and intralocus sexual conflict may prevent sex-specific diet optimization. We show that both male and female longevity were maximized on a high-carbohydrate low-protein diet in field crickets Teleogryllus commodus, but male and female lifetime reproductive performances were maximized in markedly different parts of the nutrient intake landscape. Given a choice, crickets exhibited sex-specific dietary preference in the direction that increases reproductive performance, but this sexual dimorphism in preference was incomplete, with both sexes displaced from the optimum diet for lifetime reproduction. Sexes are, therefore, constrained in their ability to reach their sex-specific dietary optima by the shared biology of diet choice. Our data suggest that sex-specific selection has thus far failed fully to resolve intralocus sexual conflict over diet optimization. Such conflict may be an important factor linking nutrition and reproduction to lifespan and aging.
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              Toll-like receptors--taking an evolutionary approach.

              The Toll receptor was initially identified in Drosophila melanogaster for its role in embryonic development. Subsequently, D. melanogaster Toll and mammalian Toll-like receptors (TLRs) have been recognized as key regulators of immune responses. After ten years of intense research on TLRs and the recent accumulation of genomic and functional data in diverse organisms, we review the distribution and functions of TLRs in the animal kingdom. We provide an evolutionary perspective on TLRs, which sheds light on their origin at the dawn of animal evolution and suggests that different TLRs might have been co-opted independently during animal evolution to mediate analogous immune functions.
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                Author and article information

                Contributors
                Journal
                Insect Biochem Mol Biol
                Insect Biochem. Mol. Biol
                Insect Biochemistry and Molecular Biology
                Elsevier Science
                0965-1748
                1879-0240
                1 June 2019
                June 2019
                : 109
                : 128-141
                Affiliations
                [a ]School of Life Sciences, University of Lincoln, Brayford Pool, Lincoln, LN6 7TS, UK
                [b ]Lancaster Environment Centre, Lancaster University, Lancaster, LA1 4YQ, UK
                [c ]Charles Perkins Centre, University of Sydney, NSW, 2006, Australia
                [d ]Department of Biological Sciences, Macquarie University, NSW, 2109, Australia
                [e ]School of Forensic and Applied Sciences, University of Central Lancashire, Preston, Lancashire, PR1 2HE, UK
                Author notes
                []Corresponding author. scotter@ 123456lincoln.ac.uk
                Article
                S0965-1748(18)30490-9
                10.1016/j.ibmb.2019.04.009
                6527921
                30954680
                a04cc5db-90f3-4b04-9780-54384aab2f01
                © 2019 The Authors

                This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

                History
                : 8 January 2019
                : 1 April 2019
                : 2 April 2019
                Categories
                Article

                nutritional ecology,host-pathogen interaction,immunity,spodoptera,xenorhabdus,diet,bacteria,resistance,tolerance,insect,geometric framework

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