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      From moths to caterpillars: Ideal conditions for Galleria mellonella rearing for in vivo microbiological studies

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          ABSTRACT

          Galleria mellonella is a well-accepted insect model for the study of pathogen-host interactions and antimicrobial compounds. The main advantages of this model include the low cost of maintenance, the fast life cycle, the possibility of using a large number of caterpillars and the innate immune system, which is evolutionarily conserved relative to mammals. Because of these advantages, different research groups have been working to implement the rearing of G. mellonella in laboratory conditions. This protocol describes our experience in the rearing of G. mellonella caterpillars for experimental infection models and the influence of different artificial diets on developmental and physiological parameters. Here, we suggest a diet composition that benefits the life cycle of G. mellonella by accelerating the larval phase length and increasing the caterpillar weight. This diet also stimulated the immune system of G. mellonella by increasing the hemolymph volume and hemocyte concentration. In addition, our rearing protocol generated caterpillars that are more resistant to infection by Staphylococcus aureus, Escherichia coli and Candida albicans. A standard G. mellonella rearing protocol is fundamental to minimize external influences on the results, and this simple and easy protocol can support researchers starting to rear G. mellonella.

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          Most cited references33

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          Galleria mellonella as a model system to study Cryptococcus neoformans pathogenesis.

          Evaluation of Cryptococcus neoformans virulence in a number of nonmammalian hosts suggests that C. neoformans is a nonspecific pathogen. We used the killing of Galleria mellonella (the greater wax moth) caterpillar by C. neoformans to develop an invertebrate host model system that can be used to study cryptococcal virulence, host immune responses to infection, and the effects of antifungal compounds. All varieties of C. neoformans killed G. mellonella. After injection into the insect hemocoel, C. neoformans proliferated and, despite successful phagocytosis by host hemocytes, killed caterpillars both at 37 degrees C and 30 degrees C. The rate and extent of killing depended on the cryptococcal strain and the number of fungal cells injected. The sequenced C. neoformans clinical strain H99 was the most virulent of the strains tested and killed caterpillars with inocula as low as 20 CFU/caterpillar. Several C. neoformans genes previously shown to be involved in mammalian virulence (CAP59, GPA1, RAS1, and PKA1) also played a role in G. mellonella killing. Combination antifungal therapy (amphotericin B plus flucytosine) administered before or after inoculation was more effective than monotherapy in prolonging survival and in decreasing the tissue burden of cryptococci in the hemocoel. The G. mellonella-C. neoformans pathogenicity model may be a substitute for mammalian models of infection with C. neoformans and may facilitate the in vivo study of fungal virulence and efficacy of antifungal therapies.
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            Growth versus lifespan: perspectives from evolutionary ecology.

            There are many ecological advantages to attaining a large body size as fast as possible (such as reduced risks of being caught by predators or increased reproductive success). However, studies in several taxa indicate that fast growth in itself can have negative as well as positive effects. There appears to be a link between accelerated growth and lifespan: rapid growth early in life is associated with impaired later performance and reduced longevity. In this review we assess the evidence for such within individual trade-offs between growth rate and lifespan, and the potential physiological mechanisms that might underlie them. We discuss the fitness implications of any reduction in lifespan, and point out that certain environmental circumstances may favour a 'grow fast and die young' strategy if this increases overall reproductive success. However, investigation of the intra-specific relationships among growth rate, lifespan and fitness is not straightforward; few studies have controlled for confounding variables such as adult body size or duration of the growth period, and none to date have measured fitness in an appropriate ecological setting. We suggest a number of experimental approaches that might allow the true relationships between growth rate and future performance to be elucidated.
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              Methods for using Galleria mellonella as a model host to study fungal pathogenesis.

              The facile inoculum delivery and handling of the insect Galleria mellonella make it a desirable model for the study of fungal pathogenesis. Here we present methods to study fungal virulence, filamentation and fungal cell associates with insect hemocytes using Candida albicans and Cryptococcus neoformans to illustrate the use of this model. The two types of fungi cause distinct infections thus we compare and contrast the infection characteristics observed in G. mellonella. The protocols presented herein can be adapted to the study of other fungal pathogens using G. mellonella as an infection model.
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                Author and article information

                Journal
                Virulence
                Virulence
                KVIR
                kvir20
                Virulence
                Taylor & Francis
                2150-5594
                2150-5608
                2018
                1 March 2018
                1 March 2018
                : 9
                : 1
                : 383-389
                Affiliations
                [a ]Department of Biosciences and Oral Diagnosis, Institute of Science and Technology, São Paulo State University (UNESP) , São José dos Campos, São Paulo, Brazil
                [b ]Empresa Brasileira de Agropecuária (Embrapa Gado de Leite) , Juiz de Fora, Minas Gerais, Brazil
                Author notes
                CONTACT Liliana Scorzoni liliscorzoni@ 123456yahoo.com.br Universidade Estadual Paulista, Júlio de Mesquita Filho- Avenida Francisco José Longo , 777 São José dos Campos/São Paulo 12245-000, Brazil
                Article
                1397871
                10.1080/21505594.2017.1397871
                5955185
                29130369
                cb4335d2-2fa6-45c2-9841-8c73732297fb
                © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group

                This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License ( http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.

                History
                : 10 May 2017
                : 23 October 2017
                : 24 October 2017
                Page count
                Figures: 4, Tables: 4, Equations: 0, References: 38, Pages: 7
                Funding
                Funded by: São Paulo Research Foundation (FAPESP)
                Award ID: 2015/09770-9
                São Paulo Research Foundation (FAPESP) ID: 2015/09770-9
                Categories
                Protocol

                Infectious disease & Microbiology
                experimental model,galleria mellonella,in vivo study,rearing
                Infectious disease & Microbiology
                experimental model, galleria mellonella, in vivo study, rearing

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