Fly iDNA suggests strict reliance of the causative agent of sylvatic anthrax on rainforest ecosystems

Author:

Jahan Mueena123ORCID,Lagostina Lorenzo12ORCID,Gräßle Tobias12ORCID,Couacy‐Hymann Emmanuel4ORCID,Kouadio Leonce45,Kouakou Valère K.4ORCID,Krou Hermann A.4,Mossoun Arsène M.4,Patrono Livia V.126ORCID,Pléh Kamilla12ORCID,Steiner Jonas A.1,Yves Noma7,Leendertz Fabian H.12ORCID,Calvignac‐Spencer Sébastien26ORCID,Gogarten Jan F.1268ORCID

Affiliation:

1. Helmholtz Institute for One Health Greifswald Germany

2. Epidemiology of Highly Pathogenic Organisms Robert Koch Institute Berlin Germany

3. Department of Microbiology and Public Health Bangabandhu Sheikh Mujibur Rahman Agricultural University Gazipur Bangladesh

4. Laboratory for Innovative Research for Emerging Diseases and Diagnostics Centre National de Recherche Agronomique, NGO One Health for All Abidjan Côte d'Ivoire

5. Université Peleforo Gon Coulibaly Korhogo Côte d'Ivoire

6. Viral Evolution, Robert Koch Institute Berlin Germany

7. Laboratoire d'écologie moléculaire et de génétique evolutive, Department of Genetics University Felix Houphouët Boigny Abidjan Côte d'Ivoire

8. Applied Zoology and Nature Conservation University of Greifswald Greifswald Germany

Abstract

AbstractMetabarcoding of invertebrate‐derived DNA (iDNA) is increasingly used to describe vertebrate diversity in terrestrial ecosystems. Fly iDNA has also shown potential as a tool for detecting pathogens. Combining these approaches makes fly iDNA a promising tool for understanding the ecology and distribution of novel pathogens or emerging infectious diseases. Here, we use fly iDNA to explore the geographic distribution of Bacillus cereus biovar anthracis (Bcbva) along a gradient from the forest within Taï National Park, Côte d'Ivoire, out to surrounding villages. We tested fly pools (N = 100 pools of 5 flies) collected in the forest (N = 25 pools), along the forest edge (N = 50 pools), and near surrounding villages (N = 25 pools) for Bcbva. Using the same iDNA, we sought to reconstruct fly and mammal communities with metabarcoding, with the aim of investigating potential links with Bcbva detection. We detected Bcbva in 5/100 fly pools and positivity varied significantly across the habitat types (forest = 4/25, edge = 1/50, village = 0/25). It was possible to culture Bcbva from all positive fly pools, confirming their positivity, while sequencing of their whole genomes revealed a considerable portion of known genomic diversity for this pathogen. iDNA generated data about the mammal and fly communities in these habitats, revealing the highest mammal diversity in the forest and considerable changes in fly community composition along the gradient. Bcbva host range estimates from fly iDNA were largely identical to the results of long‐term carcass monitoring efforts in the region. We show that fly iDNA can generate data on the geographic distribution and host range of a pathogen at kilometer scales, as well as reveal the pathogen's phylogenetic diversity. Our results highlight the power of fly iDNA for mammal biomonitoring and pathogen surveillance.

Funder

Deutsche Forschungsgemeinschaft

European Commission

Ministry of Science and Technology, Government of the People’s Republic of Bangladesh

Publisher

Wiley

Subject

Genetics,Ecology,Ecology, Evolution, Behavior and Systematics

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