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Detection of SARS-CoV-2 Omicron variant (B.1.1.529) infection of white-tailed deer

White-tailed deer (Odocoileus virginianus) are highly susceptible to infection by SARS-CoV-2, with multiple reports of widespread spillover of virus from humans to free-living deer. While the recently emerged SARS-CoV-2 B.1.1.529 Omicron variant of concern (VoC) has been shown to be notably more tra...

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Autores principales: Vandegrift, Kurt J., Yon, Michele, Surendran-Nair, Meera, Gontu, Abhinay, Amirthalingam, Saranya, Nissly, Ruth H., Levine, Nicole, Stuber, Tod, DeNicola, Anthony J., Boulanger, Jason R., Kotschwar, Nathan, Aucoin, Sarah Grimké, Simon, Richard, Toal, Katrina, Olsen, Randall J., Davis, James J., Bold, Dashzeveg, Gaudreault, Natasha N., Richt, Juergen A., Musser, James M., Hudson, Peter J., Kapur, Vivek, Kuchipudi, Suresh V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8845426/
https://www.ncbi.nlm.nih.gov/pubmed/35169802
http://dx.doi.org/10.1101/2022.02.04.479189
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author Vandegrift, Kurt J.
Yon, Michele
Surendran-Nair, Meera
Gontu, Abhinay
Amirthalingam, Saranya
Nissly, Ruth H.
Levine, Nicole
Stuber, Tod
DeNicola, Anthony J.
Boulanger, Jason R.
Kotschwar, Nathan
Aucoin, Sarah Grimké
Simon, Richard
Toal, Katrina
Olsen, Randall J.
Davis, James J.
Bold, Dashzeveg
Gaudreault, Natasha N.
Richt, Juergen A.
Musser, James M.
Hudson, Peter J.
Kapur, Vivek
Kuchipudi, Suresh V.
author_facet Vandegrift, Kurt J.
Yon, Michele
Surendran-Nair, Meera
Gontu, Abhinay
Amirthalingam, Saranya
Nissly, Ruth H.
Levine, Nicole
Stuber, Tod
DeNicola, Anthony J.
Boulanger, Jason R.
Kotschwar, Nathan
Aucoin, Sarah Grimké
Simon, Richard
Toal, Katrina
Olsen, Randall J.
Davis, James J.
Bold, Dashzeveg
Gaudreault, Natasha N.
Richt, Juergen A.
Musser, James M.
Hudson, Peter J.
Kapur, Vivek
Kuchipudi, Suresh V.
author_sort Vandegrift, Kurt J.
collection PubMed
description White-tailed deer (Odocoileus virginianus) are highly susceptible to infection by SARS-CoV-2, with multiple reports of widespread spillover of virus from humans to free-living deer. While the recently emerged SARS-CoV-2 B.1.1.529 Omicron variant of concern (VoC) has been shown to be notably more transmissible amongst humans, its ability to cause infection and spillover to non-human animals remains a challenge of concern. We found that 19 of the 131 (14.5%; 95% CI: 0.10–0.22) white-tailed deer opportunistically sampled on Staten Island, New York, between December 12, 2021, and January 31, 2022, were positive for SARS-CoV-2 specific serum antibodies using a surrogate virus neutralization assay, indicating prior exposure. The results also revealed strong evidence of age-dependence in antibody prevalence. A significantly (χ(2), p < 0.001) greater proportion of yearling deer possessed neutralizing antibodies as compared with fawns (OR=12.7; 95% CI 4–37.5). Importantly, SARS-CoV-2 nucleic acid was detected in nasal swabs from seven of 68 (10.29%; 95% CI: 0.0–0.20) of the sampled deer, and whole-genome sequencing identified the SARS-CoV-2 Omicron VoC (B.1.1.529) is circulating amongst the white-tailed deer on Staten Island. Phylogenetic analyses revealed the deer Omicron sequences clustered closely with other, recently reported Omicron sequences recovered from infected humans in New York City and elsewhere, consistent with human to deer spillover. Interestingly, one individual deer was positive for viral RNA and had a high level of neutralizing antibodies, suggesting either rapid serological conversion during an ongoing infection or a “breakthrough” infection in a previously exposed animal. Together, our findings show that the SARS-CoV-2 B.1.1.529 Omicron VoC can infect white-tailed deer and highlights an urgent need for comprehensive surveillance of susceptible animal species to identify ecological transmission networks and better assess the potential risks of spillback to humans.
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spelling pubmed-88454262022-02-16 Detection of SARS-CoV-2 Omicron variant (B.1.1.529) infection of white-tailed deer Vandegrift, Kurt J. Yon, Michele Surendran-Nair, Meera Gontu, Abhinay Amirthalingam, Saranya Nissly, Ruth H. Levine, Nicole Stuber, Tod DeNicola, Anthony J. Boulanger, Jason R. Kotschwar, Nathan Aucoin, Sarah Grimké Simon, Richard Toal, Katrina Olsen, Randall J. Davis, James J. Bold, Dashzeveg Gaudreault, Natasha N. Richt, Juergen A. Musser, James M. Hudson, Peter J. Kapur, Vivek Kuchipudi, Suresh V. bioRxiv Article White-tailed deer (Odocoileus virginianus) are highly susceptible to infection by SARS-CoV-2, with multiple reports of widespread spillover of virus from humans to free-living deer. While the recently emerged SARS-CoV-2 B.1.1.529 Omicron variant of concern (VoC) has been shown to be notably more transmissible amongst humans, its ability to cause infection and spillover to non-human animals remains a challenge of concern. We found that 19 of the 131 (14.5%; 95% CI: 0.10–0.22) white-tailed deer opportunistically sampled on Staten Island, New York, between December 12, 2021, and January 31, 2022, were positive for SARS-CoV-2 specific serum antibodies using a surrogate virus neutralization assay, indicating prior exposure. The results also revealed strong evidence of age-dependence in antibody prevalence. A significantly (χ(2), p < 0.001) greater proportion of yearling deer possessed neutralizing antibodies as compared with fawns (OR=12.7; 95% CI 4–37.5). Importantly, SARS-CoV-2 nucleic acid was detected in nasal swabs from seven of 68 (10.29%; 95% CI: 0.0–0.20) of the sampled deer, and whole-genome sequencing identified the SARS-CoV-2 Omicron VoC (B.1.1.529) is circulating amongst the white-tailed deer on Staten Island. Phylogenetic analyses revealed the deer Omicron sequences clustered closely with other, recently reported Omicron sequences recovered from infected humans in New York City and elsewhere, consistent with human to deer spillover. Interestingly, one individual deer was positive for viral RNA and had a high level of neutralizing antibodies, suggesting either rapid serological conversion during an ongoing infection or a “breakthrough” infection in a previously exposed animal. Together, our findings show that the SARS-CoV-2 B.1.1.529 Omicron VoC can infect white-tailed deer and highlights an urgent need for comprehensive surveillance of susceptible animal species to identify ecological transmission networks and better assess the potential risks of spillback to humans. Cold Spring Harbor Laboratory 2022-02-07 /pmc/articles/PMC8845426/ /pubmed/35169802 http://dx.doi.org/10.1101/2022.02.04.479189 Text en https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Vandegrift, Kurt J.
Yon, Michele
Surendran-Nair, Meera
Gontu, Abhinay
Amirthalingam, Saranya
Nissly, Ruth H.
Levine, Nicole
Stuber, Tod
DeNicola, Anthony J.
Boulanger, Jason R.
Kotschwar, Nathan
Aucoin, Sarah Grimké
Simon, Richard
Toal, Katrina
Olsen, Randall J.
Davis, James J.
Bold, Dashzeveg
Gaudreault, Natasha N.
Richt, Juergen A.
Musser, James M.
Hudson, Peter J.
Kapur, Vivek
Kuchipudi, Suresh V.
Detection of SARS-CoV-2 Omicron variant (B.1.1.529) infection of white-tailed deer
title Detection of SARS-CoV-2 Omicron variant (B.1.1.529) infection of white-tailed deer
title_full Detection of SARS-CoV-2 Omicron variant (B.1.1.529) infection of white-tailed deer
title_fullStr Detection of SARS-CoV-2 Omicron variant (B.1.1.529) infection of white-tailed deer
title_full_unstemmed Detection of SARS-CoV-2 Omicron variant (B.1.1.529) infection of white-tailed deer
title_short Detection of SARS-CoV-2 Omicron variant (B.1.1.529) infection of white-tailed deer
title_sort detection of sars-cov-2 omicron variant (b.1.1.529) infection of white-tailed deer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8845426/
https://www.ncbi.nlm.nih.gov/pubmed/35169802
http://dx.doi.org/10.1101/2022.02.04.479189
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