1. Biodiversity and vector‐borne diseases: Host dilution and vector amplification occur simultaneously for Amazonian leishmaniases
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Arthur Kocher, Josselin Cornuault, Jean‐Charles Gantier, Sophie Manzi, Agathe Chavy, Romain Girod, Isabelle Dusfour, Pierre‐Michel Forget, Marine Ginouves, Ghislaine Prévot, Jean‐François Guégan, Anne‐Laure Bañuls, Benoît de Thoisy, Jérôme Murienne, Evolution et Diversité Biologique (EDB), Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Université de Toulouse (UT)-Centre National de la Recherche Scientifique (CNRS), Institut Pasteur de la Guyane, Réseau International des Instituts Pasteur (RIIP), Max Planck Institute for the Science of Human History (MPI-SHH), Max-Planck-Gesellschaft, Maladies infectieuses et vecteurs : écologie, génétique, évolution et contrôle (MIVEGEC), Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD [France-Sud])-Université de Montpellier (UM), Real Jardín Botánico de Madrid (RJB), Spanish National Research Council (CSIC), Institut des Sciences de l'Evolution de Montpellier (UMR ISEM), Centre de Coopération Internationale en Recherche Agronomique pour le Développement (Cirad)-École Pratique des Hautes Études (EPHE), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Institut de recherche pour le développement [IRD] : UR226-Centre National de la Recherche Scientifique (CNRS)-Université de Montpellier (UM), Laboratoire Identifications Fongiques et Entomo-Parasitologique (L.I.F.E.), Université de Guyane (UG), Mécanismes Adaptatifs et Evolution (MECADEV), Muséum national d'Histoire naturelle (MNHN)-Centre National de la Recherche Scientifique (CNRS), Centre d’Infection et d’Immunité de Lille - INSERM U 1019 - UMR 9017 - UMR 8204 (CIIL), Institut Pasteur de Lille, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille)-Centre National de la Recherche Scientifique (CNRS), Institut de Recherche pour le Développement (IRD [France-Sud]), Animal, Santé, Territoires, Risques et Ecosystèmes (UMR ASTRE), Centre de Coopération Internationale en Recherche Agronomique pour le Développement (Cirad)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE), Association Kwata - Etude et protection de la nature [Guyane], Fondation de France, European Regional Development Fund, H2020 Marie Sklodowska-Curie Actions, Grant/Award Number: MSCAIF-EF-ST-708207, Agence Nationale de la Recherche, Grant/Award Number: ANR-10-LABX-25-01, ANR-10-LABX-41, ANR-11-INBS-0001 and ANR-11-LABX--0010-DRIIHM, NSF-NIH Ecology of infectious diseases award, Grant/Award Number: 191145, ANR-10-LABX-0041,TULIP,Towards a Unified theory of biotic Interactions: the roLe of environmental(2010), ANR-11-INBS-0001,ANAEE-FR,ANAEE-Services(2011), ANR-11-LABX-0010,DRIIHM / IRDHEI,Dispositif de recherche interdisciplinaire sur les Interactions Hommes-Milieux(2011), and ANR-10-LABX-0025,CEBA,CEnter of the study of Biodiversity in Amazonia(2010)
- Subjects
amplification effect ,Culicidae ,iDNA ,[SDV]Life Sciences [q-bio] ,dilution effect ,metabarcoding ,fungi ,parasitic diseases ,Genetics ,phlebotomine sand fly ,Ecology, Evolution, Behavior and Systematics ,zoonotic disease - Abstract
Changes in biodiversity may impact infectious disease transmission through multiple mechanisms. We explored the impact of biodiversity changes on the transmission of Amazonian leishmaniases, a group of wild zoonoses transmitted by phlebotomine sand flies (Psychodidae), which represent an important health burden in a region where biodiversity is both rich and threatened. Using molecular analyses of sand fly pools and blood-fed dipterans, we characterized the disease system in forest sites in French Guiana undergoing different levels of human-induced disturbance. We show that the prevalence of Leishmania parasites in sand flies correlates positively with the relative abundance of mammal species known as Leishmania reservoirs. In addition, Leishmania reservoirs tend to dominate in less diverse mammal communities, in accordance with the dilution effect hypothesis. This results in a negative relationship between Leishmania prevalence and mammal diversity. On the other hand, higher mammal diversity is associated with higher sand fly density, possibly because more diverse mammal communities harbor higher biomass and more abundant feeding resources for sand flies, although more research is needed to identify the factors that shape sand fly communities. As a consequence of these antagonistic effects, decreased mammal diversity comes with an increase of parasite prevalence in sand flies, but has no detectable impact on the density of infected sand flies. These results represent additional evidence that biodiversity changes may simultaneously dilute and amplify vector-borne disease transmission through different mechanisms that need to be better understood before drawing generalities on the biodiversity-disease relationship. 1 Introduction 2 Material and methods 2.1 Sampling 2.2 Laboratory 2.3 Bioinformatic analyses 2.4 Estimating mammal diversity from individual dipteran blood meals 2.5 Effect of mammal diversity on Leishmania transmission 3 Results 3.1 Sampling and molecular analyses 3.2 Sand fly, vertebrate and Leishmania identifications 3.3 Statistical analyses 4 Discussion
- Published
- 2022
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