As disease regulation is a key ecosystem service, it is crucial that we better understand the role that restoring landscapes can play in reducing disease risks. Ongoing One Health studies suggest that declining biodiversity and increasing zoonotic pathogen spill-over risk are linked. Restoration processes normally aim at increasing species diversity, wherefore it is assumed that pathogens will be diluted in restored ecosystems, hence reducing the risk of zoonotic spillover. Nonetheless, the developing species composition during restorative processes will impact dilution-amplification effects. To estimate the threshold beyond which a restored ecosystem can be considered to have reached the pathogen dilution phase, it is crucial to characterise the communities of hosts, and the prevalence of pathogens, at the different stages of recovery of an ecosystem. Using interdisciplinary methods, this project has the dual aim of examining the amplification-dilution of zoonotic pathogens in a mangrove forest of the western Peninsular Malaysia, and to estimate the frequency and duration of exposure of local communities to this hazard, so as to best mitigate the risk of zoonotic pathogen spillover.
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The processes involved in acquiring, trading, preparing, and consuming wild meat pose significant risks for the emergence of zoonotic infectious diseases. Several major viral outbreaks have been directly linked to the wild meat supply chain, yet our knowledge of the virome in many mammals involved in this chain remains limited and disproportionately focused on certain mammalian taxa and pathogens. This report presents the findings of a metagenomic viral screening of 99 specimens belonging to 27 wild African mammal species and one domesticated species, all traded for their meat. The study focuses on tissue and swab samples collected from various regions in the Democratic Republic of the Congo and in Brussels, Belgium. A total of fifteen virus strains were detected, belonging to the families Arteriviridae, Retroviridae and Sedoreoviridae (primates), Picobirnaviridae (primates and rodents), Picornaviridae (rodents), Hepadnaviridae (hyrax), Orthoherpesviridae (artiodactylid and carnivore) and Spinareoviridae (carnivore). Several strains were detected in mammalian hosts for the first time, expanding their host range and genetic diversity. Of note is the presence of viruses genetically related to recognised zoonotic pathogens, i.e., human picobirnavirus (Orthopicobirnavirus hominis) (primates and rodents), simian foamy viruses (Simiispumavirus) (primates), and rotavirus A (Rotavirus alphagastroenteritidis) (primates). The presence of these viruses in primates is concerning as non-human primates are phylogenetically closely related to humans, which can facilitate interspecies viral transmission. These findings underscore the high diversity of mammalian viruses and the potential risk of human infection through cross-species transmission during the close interactions with wildlife in the wild meat supply chain.
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