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      Analysis of the early cellular and humoral responses of Galleria mellonella larvae to infection by Candida albicans

      research-article
      ,
      Virulence
      Taylor & Francis
      candida, galleria, immunity, infection, in vivo screening, Mini-model

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          ABSTRACT

          Galleria mellonella larvae were administered an inoculum of Candida albicans and the response to infection over 24 hours was monitored. The yeast cell density in infected larvae declined initially but replication commenced six hours post-infection. The hemocyte density decreased from 5.2 × 10 6/ml to 2.5 × 10 6/ml at 2 hours but increased to 4.2 × 106 at 6 hours and decreased subsequently. Administration of β – glucan to larvae also caused a fluctuation in hemocyte density (5.1 ± 0.22 × 10 6/ml (0 hour) to 6.25 ± 0.25 × 106/ml (6 hour) (p < 0.05) to 5 ± 2.7 × 106 (24 hour)) and the population showed an increase in the density of small, granular cells at 24 hours (p < 0.05). Hemocytes from larvae inoculated with β – glucan for 6 or 24 hours showed faster killing of C. albicans cells (53 ± 4.1% (p < 0.01), 64 ± 3.7%, (p < 0.01), respectively) than hemocytes from control larvae (24 ± 11%) at 60 min. Proteomic analysis indicated increased abundance of immune related proteins cecropin-A (5 fold) and prophenoloxidase-activating proteinase-1 (5 fold) 6 hours post infection but by 24 hours there was elevated abundance of muscle (tropomyosin 2 (141 fold), calponin (66 fold), troponin I (62 fold)) and proteins indicative of cellular stress (glutathione-S-transferase-like protein (114 fold)), fungal dissemination (muscle protein 20-like protein (174 fold)) and tissue breakdown (mitochondrial cytochrome c (10 fold)). Proteins decreased in abundance at 24 hour included β – 1,3 – glucan recognition protein precursor (29 fold) and prophenoloxidase subunit 2 (25 fold).

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          Most cited references40

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          Positive correlation between virulence of Pseudomonas aeruginosa mutants in mice and insects.

          Strain PA14, a human clinical isolate of Pseudomonas aeruginosa, is pathogenic in mice and insects (Galleria mellonella). Analysis of 32 different PA14 mutants in these two hosts showed a novel positive correlation in the virulence patterns. Thus, G. mellonella is a good model system for identifying mammalian virulence factors of P. aeruginosa.
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            Organ-specific innate immune responses in a mouse model of invasive candidiasis.

            In a fatal mouse model of invasive candidiasis (IC), fungal burden changes with variable dynamics in the kidney, brain, spleen, and liver and declines in all organs except for the kidney, which inexorably loses function. Since leukocytes are required to control Candida, we hypothesized that differential leukocyte infiltration determines organ-specific outcome of the infection. We defined leukocyte accumulation in the blood, kidney, brain, spleen, and liver after infection using fluorescent-activated cell sorting (FACS) and immunohistochemistry. Accumulation of Ly6c(int)CD11b(+) neutrophils predominated in all organs except the brain, where CD45(int)CD11b(+)CD11c(-) microglia were the major leukocytes detected, surrounding foci of invading Candida. Significantly more neutrophils accumulated in the spleen and liver than in the kidney during the first 24 h after infection, when neutrophil presence is critical for Candida control. Conversely, at later time points only the kidney continued to accumulate neutrophils, associated with immunopathology and organ failure. The distribution of neutrophils was completely different in each organ, with large abscesses exclusively forming in the kidney. Candida filamentation, an essential virulence factor, was seen in the kidney but not in the spleen or liver. IC induced Ly6c(hi)CD11b(+) inflammatory monocyte and NK1.1(+) cell expansion in the blood and all organs tested, and MHCII(+)F4/80(+)CD11c(-) macrophage accumulation, mainly in the spleen and liver. This study is the first detailed analysis of leukocyte subsets accumulating in different target organs during IC. The results delineate immune responses to the same pathogen that are highly idiosyncratic for each organ tested. The work provides novel insights into the balance between effective host defense and immunopathology in IC. Copyright © 2010 S. Karger AG, Basel.
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              An analysis of the structural and functional similarities of insect hemocytes and mammalian phagocytes

              The insect immune response demonstrates a number of structural and functional similarities to the innate immune system of mammals. As a result of these conserved features insects have become popular choices for evaluating the virulence of microbial pathogens or for assessing the efficacy of antimicrobial agents and give results which are comparable to those that can be obtained using mammals. Analysis of the cellular component of the insect and mammalian immune systems demonstrates many similarities. Insect hemocytes recognize pathogens and phagocytose material in a similar manner to neutrophils. The killing of ingested microbes is achieved in both cell types by the production of superoxide and by the release of enzymes in the process of degranulation. Insect hemocytes and mammalian neutrophils are sensitive to the same inhibitors. This review highlights the strong similarities between the phagocytic cells of both groups of animals and demonstrates the potential benefits of using selected insects as in vivo screening systems.
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                Author and article information

                Journal
                Virulence
                Virulence
                KVIR
                kvir20
                Virulence
                Taylor & Francis
                2150-5594
                2150-5608
                2018
                21 September 2017
                21 September 2017
                : 9
                : 1
                : 163-172
                Affiliations
                Department of Biology, Maynooth University , Maynooth, Co. Kildare, Ireland
                Author notes
                CONTACT Prof. Kevin Kavanagh kevin.kavanagh@ 123456nuim.ie Department of Biology, Maynooth University , Co. Room 2.40, Callan Building, Maynooth, Kildare, Ireland
                Article
                1370174
                10.1080/21505594.2017.1370174
                5955201
                28872999
                7e58403a-c9b1-428a-aeb4-9237d8aedaa3
                © 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 License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 10 May 2017
                : 11 August 2017
                : 17 August 2017
                Page count
                Figures: 5, Tables: 0, Equations: 0, References: 45, Pages: 10
                Categories
                Research Paper

                Infectious disease & Microbiology
                candida,galleria,immunity,infection,in vivo screening,mini-model
                Infectious disease & Microbiology
                candida, galleria, immunity, infection, in vivo screening, mini-model

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