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      Interacting Symbionts and Immunity in the Amphibian Skin Mucosome Predict Disease Risk and Probiotic Effectiveness

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          Abstract

          Pathogenesis is strongly dependent on microbial context, but development of probiotic therapies has neglected the impact of ecological interactions. Dynamics among microbial communities, host immune responses, and environmental conditions may alter the effect of probiotics in human and veterinary medicine, agriculture and aquaculture, and the proposed treatment of emerging wildlife and zoonotic diseases such as those occurring on amphibians or vectored by mosquitoes. Here we use a holistic measure of amphibian mucosal defenses to test the effects of probiotic treatments and to assess disease risk under different ecological contexts. We developed a non-invasive assay for antifungal function of the skin mucosal ecosystem (mucosome function) integrating host immune factors and the microbial community as an alternative to pathogen exposure experiments. From approximately 8500 amphibians sampled across Europe, we compared field infection prevalence with mucosome function against the emerging fungal pathogen Batrachochytrium dendrobatidis. Four species were tested with laboratory exposure experiments, and a highly susceptible species, Alytes obstetricans, was treated with a variety of temperature and microbial conditions to test the effects of probiotic therapies and environmental conditions on mucosome function. We found that antifungal function of the amphibian skin mucosome predicts the prevalence of infection with the fungal pathogen in natural populations, and is linked to survival in laboratory exposure experiments. When altered by probiotic therapy, the mucosome increased antifungal capacity, while previous exposure to the pathogen was suppressive. In culture, antifungal properties of probiotics depended strongly on immunological and environmental context including temperature, competition, and pathogen presence. Functional changes in microbiota with shifts in temperature provide an alternative mechanistic explanation for patterns of disease susceptibility related to climate beyond direct impact on host or pathogen. This nonlethal management tool can be used to optimize and quickly assess the relative benefits of probiotic therapies under different climatic, microbial, or host conditions.

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          Multiple emergences of genetically diverse amphibian-infecting chytrids include a globalized hypervirulent recombinant lineage.

          Batrachochytrium dendrobatidis (Bd) is a globally ubiquitous fungal infection that has emerged to become a primary driver of amphibian biodiversity loss. Despite widespread effort to understand the emergence of this panzootic, the origins of the infection, its patterns of global spread, and principle mode of evolution remain largely unknown. Using comparative population genomics, we discovered three deeply diverged lineages of Bd associated with amphibians. Two of these lineages were found in multiple continents and are associated with known introductions by the amphibian trade. We found that isolates belonging to one clade, the global panzootic lineage (BdGPL) have emerged across at least five continents during the 20th century and are associated with the onset of epizootics in North America, Central America, the Caribbean, Australia, and Europe. The two newly identified divergent lineages, Cape lineage (BdCAPE) and Swiss lineage (BdCH), were found to differ in morphological traits when compared against one another and BdGPL, and we show that BdGPL is hypervirulent. BdGPL uniquely bears the hallmarks of genomic recombination, manifested as extensive intergenomic phylogenetic conflict and patchily distributed heterozygosity. We postulate that contact between previously genetically isolated allopatric populations of Bd may have allowed recombination to occur, resulting in the generation, spread, and invasion of the hypervirulent BdGPL leading to contemporary disease-driven losses in amphibian biodiversity.
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            The skin microbiome

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              Modulating immunity as a therapy for bacterial infections.

              Despite our efforts to halt the increase and spread of antimicrobial resistance, bacteria continue to become less susceptible to antimicrobial drugs over time, and rates of discovery for new antibiotics are declining. Thus, it is essential to explore new paradigms for anti-infective therapy. One promising approach involves host-directed immunomodulatory therapies, whereby natural mechanisms in the host are exploited to enhance therapeutic benefit. The objective is to initiate or enhance protective antimicrobial immunity while limiting inflammation-induced tissue injury. A range of potential immune modulators have been proposed, including innate defence regulator peptides and agonists of innate immune components such as Toll-like receptors and NOD-like receptors.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2014
                30 April 2014
                : 9
                : 4
                : e96375
                Affiliations
                [1 ]Institute of Evolutionary Biology and Environmental Studies, University of Zurich, Zurich, Switzerland
                [2 ]Department of Ecology and Evolutionary Biology, University of Colorado, Boulder, Colorado, United States of America
                [3 ]Section for Freshwater Biology, Department of Biology, University of Copenhagen, Copenhagen, Denmark
                [4 ]Department of Evolutionary Biology, Technical University of Braunschweig, Braunschweig, Germany
                [5 ]KARCH, Neuchâtel, Switzerland
                [6 ]Howard Hughes Medical Institute and Department of Chemistry and Biochemistry, BioFrontiers Institute, University of Colorado, Boulder, Colorado, United States of America
                University of Sao Paulo, Brazil
                Author notes

                Competing Interests: The authors hereby confirm that co-author B. Schmidt is a PLOS ONE Editorial Board member. This does not alter their adherence to PLOS ONE Editorial policies and criteria.

                Conceived and designed the experiments: DCW SB JK EK UT. Performed the experiments: DCW HB SB JK EK UT LRD CB SH. Analyzed the data: DCW SB JK EK UT BRS. Wrote the paper: DCW BRS RK VM. Performed field work: DCW JK UT LRD.

                [¤a]

                Current address: Department of Biology, University of Massachusetts Boston, Boston, Massachusetts, United States of America

                [¤b]

                Current address: Department of Aquatic Ecology, Duebendorf, Switzerland, and Institute of Integrative Biology, ETH-Zürich, Zurich, Switzerland

                [¤c]

                Current address: Section for Freshwater Biology, Department of Biology, University of Copenhagen, Copenhagen, Denmark and Center for Macroecology, Evolution and Climate Natural History Museum of Denmark, Copenhagen, Denmark

                Article
                PONE-D-14-00836
                10.1371/journal.pone.0096375
                4005770
                24789229
                6e7dd383-709c-45ec-b643-370a393cf3d9
                Copyright @ 2014

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 9 January 2014
                : 4 April 2014
                Page count
                Pages: 13
                Funding
                Financial support came from the Zoological Institute and the Forschungskredit of the University of Zurich, Vontobel Stiftung, Janggen-Pöhn Stiftung, Basler Stiftung für biologische Forschung, Stiftung Dr. Joachim De Giacomi, Zoo Zürich, Grün Stadt Zürich, European Union of Aquarium Curators, Schweizer Tierschutz, Zürcher Tierschutz, Claraz Foundation, the environment departments of the cantons St. Gallen and Zurich, Swiss National Science Foundation (31-125099 to DCW), and U.S. National Science Foundation Population and Community Ecology Section (DEB 1146284 to VJM and RK). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology and Life Sciences
                Immunology
                Microbiology
                Ecology and Environmental Sciences
                Medicine and Health Sciences
                Pathology and Laboratory Medicine
                Pathogenesis
                Host-Pathogen Interactions

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                Uncategorized

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