TY - JOUR
T1 - New World camelids are sentinels for the presence of Borna disease virus
AU - Malbon, Alexandra J.
AU - Dürrwald, Ralf
AU - Kolodziejek, Jolanta
AU - Nowotny, Norbert
AU - Kobera, Ralph
AU - Pöhle, Dietrich
AU - Muluneh, Aemero
AU - Dervas, Eva
AU - Cebra, Christopher
AU - Steffen, Frank
AU - Paternoster, Giulia
AU - Gerspach, Christian
AU - Hilbe, Monika
N1 - Funding Information:
We thank the technical staff of the Institute of Veterinary Pathology, University of Zurich, for their excellent preparations, as well as Dr. Sibylle Herzog, Justus-Liebig-University Giessen, for determining antibody titres and Dr. Lothar Stitz, Friedrich-Loeffler-Institut Tübingen for providing monoclonal antibodies.
Publisher Copyright:
© 2021 The Authors. Transboundary and Emerging Diseases published by Wiley-VCH GmbH.
PY - 2022/3
Y1 - 2022/3
N2 - Borna disease (BD), a frequently fatal neurologic disorder caused by Borna disease virus 1 (BoDV-1), has been observed for decades in horses, sheep, and other mammals in certain regions of Europe. The bicoloured white-toothed shrew (Crocidura leucodon) was identified as a persistently infected species involved in virus transmission. Recently, BoDV-1 attracted attention as a cause of fatal encephalitis in humans. Here, we report investigations on BoDV-1-infected llamas from a farm in a BD endemic area of Switzerland, and alpacas from holdings in a region of Germany where BD was last seen in the 1960s but not thereafter. All New World camelids showed apathy and abnormal behaviour, necessitating euthanasia. Histologically, severe non-suppurative meningoencephalitis with neuronal Joest-Degen inclusion bodies was observed. BoDV-1 was confirmed by immunohistology, RT-qPCR, and sequencing in selected animals. Analysis of the llama herd over 20 years showed that losses due to clinically suspected BD increased within the last decade. BoDV-1 whole-genome sequences from one Swiss llama and one German alpaca and—for comparison—from one Swiss horse and one German shrew were established. They represent the first published whole-genome sequences of BoDV-1 clusters 1B and 3, respectively. Our analysis suggests that New World camelids may have a role as a sentinel species for BoDV-1 infection, even when symptomatic cases are lacking in other animal species.
AB - Borna disease (BD), a frequently fatal neurologic disorder caused by Borna disease virus 1 (BoDV-1), has been observed for decades in horses, sheep, and other mammals in certain regions of Europe. The bicoloured white-toothed shrew (Crocidura leucodon) was identified as a persistently infected species involved in virus transmission. Recently, BoDV-1 attracted attention as a cause of fatal encephalitis in humans. Here, we report investigations on BoDV-1-infected llamas from a farm in a BD endemic area of Switzerland, and alpacas from holdings in a region of Germany where BD was last seen in the 1960s but not thereafter. All New World camelids showed apathy and abnormal behaviour, necessitating euthanasia. Histologically, severe non-suppurative meningoencephalitis with neuronal Joest-Degen inclusion bodies was observed. BoDV-1 was confirmed by immunohistology, RT-qPCR, and sequencing in selected animals. Analysis of the llama herd over 20 years showed that losses due to clinically suspected BD increased within the last decade. BoDV-1 whole-genome sequences from one Swiss llama and one German alpaca and—for comparison—from one Swiss horse and one German shrew were established. They represent the first published whole-genome sequences of BoDV-1 clusters 1B and 3, respectively. Our analysis suggests that New World camelids may have a role as a sentinel species for BoDV-1 infection, even when symptomatic cases are lacking in other animal species.
KW - Borna disease virus
KW - Bornavirus
KW - New World camelids
KW - alpaca
KW - encephalitis
KW - llama
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U2 - 10.1111/tbed.14003
DO - 10.1111/tbed.14003
M3 - Article
C2 - 33501762
AN - SCOPUS:85101158216
SN - 1865-1674
VL - 69
SP - 451
EP - 464
JO - Transboundary and Emerging Diseases
JF - Transboundary and Emerging Diseases
IS - 2
ER -