Unbiased Virus Detection in a Danish Zoo Using a Portable Metagenomic Sequencing System

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Metagenomic next-generation sequencing (mNGS) is receiving increased attention for the detection of new viruses and infections occurring at the human–animal interface. The ability to actively transport and relocate this technology enables in situ virus identification, which could reduce response time and enhance disease management. In a previous study, we developed a straightforward mNGS procedure that greatly enhances the detection of RNA and DNA viruses in human clinical samples. In this study, we improved the mNGS protocol with transportable battery-driven equipment for the portable, non-targeted detection of RNA and DNA viruses in animals from a large zoological facility, to simulate a field setting for point-of-incidence virus detection. From the resulting metagenomic data, we detected 13 vertebrate viruses from four major virus groups: (+)ssRNA, (+)ssRNA-RT, dsDNA and (+)ssDNA, including avian leukosis virus in domestic chickens (Gallus gallus), enzootic nasal tumour virus in goats (Capra hircus) and several small, circular, Rep-encoding, ssDNA (CRESS DNA) viruses in several mammal species. More significantly, we demonstrate that the mNGS method is able to detect potentially lethal animal viruses, such as elephant endotheliotropic herpesvirus in Asian elephants (Elephas maximus) and the newly described human-associated gemykibivirus 2, a human-to-animal cross-species virus, in a Linnaeus two-toed sloth (Choloepus didactylus) and its enclosure, for the first time.

OriginalsprogEngelsk
Artikelnummer1399
TidsskriftViruses
Vol/bind15
Udgave nummer6
ISSN1999-4915
DOI
StatusUdgivet - 2023

Bibliografisk note

Funding Information:
The authors would like to thank Morten Rasmussen, Susanne Lopez Rasmussen, Dennis Jelsbak Schmidt, Katrine Kastberg and Randi Thøgersen for their participation in mNGS assay validation at the Statens Serum Institut, Denmark. The authors would also like to acknowledge Sara Abreu, Tina Christensen, Carsten Grøndahl and the zookeeper staff at Copenhagen Zoo for showing receptiveness and aid with collecting samples. Lastly, we would like to acknowledge Christina Hvilsom and Zoological Director Mads Frost Bertelsen for support and facilitation of this project in Copenhagen Zoo. This work was conducted as part of the TELE-Vir project, supported by funding from the European Union’s Horizon 2020 Research and Innovation program under grant agreement No. 773830: One Health European Joint Programme.

Publisher Copyright:
© 2023 by the authors.

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