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Evolutionary rate of SARS-CoV-2 increases during zoonotic infection of farmed mink
To investigate genetic signatures of adaptation to the mink host, we characterised the evolutionary rate heterogeneity in mink-associated severe acute respiratory syndrome coronaviruses (SARS-CoV-2). In 2020, the first detected anthropozoonotic spillover event of SARS-CoV-2 occurred in mink farms th...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9896948/ https://www.ncbi.nlm.nih.gov/pubmed/36751428 http://dx.doi.org/10.1093/ve/vead002 |
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author | Porter, Ashleigh F Purcell, Damian F J Howden, Benjamin P Duchene, Sebastian |
author_facet | Porter, Ashleigh F Purcell, Damian F J Howden, Benjamin P Duchene, Sebastian |
author_sort | Porter, Ashleigh F |
collection | PubMed |
description | To investigate genetic signatures of adaptation to the mink host, we characterised the evolutionary rate heterogeneity in mink-associated severe acute respiratory syndrome coronaviruses (SARS-CoV-2). In 2020, the first detected anthropozoonotic spillover event of SARS-CoV-2 occurred in mink farms throughout Europe and North America. Both spill-back of mink-associated lineages into the human population and the spread into the surrounding wildlife were reported, highlighting the potential formation of a zoonotic reservoir. Our findings suggest that the evolutionary rate of SARS-CoV-2 underwent an episodic increase upon introduction into the mink host before returning to the normal range observed in humans. Furthermore, SARS-CoV-2 lineages could have circulated in the mink population for a month before detection, and during this period, evolutionary rate estimates were between 3 × 10(–3) and 1.05 × 10(–2) (95 per cent HPD, with a mean rate of 6.59 × 10(–3)) a four- to thirteen-fold increase compared to that in humans. As there is evidence for unique mutational patterns within mink-associated lineages, we explored the emergence of four mink-specific Spike protein amino acid substitutions Y453F, S1147L, F486L, and Q314K. We found that mutation Y453F emerged early in multiple mink outbreaks and that mutations F486L and Q314K may co-occur. We suggest that SARS-CoV-2 undergoes a brief, but considerable, increase in evolutionary rate in response to greater selective pressures during species jumps, which may lead to the occurrence of mink-specific mutations. These findings emphasise the necessity of ongoing surveillance of zoonotic SARS-CoV-2 infections in the future. |
format | Online Article Text |
id | pubmed-9896948 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-98969482023-02-06 Evolutionary rate of SARS-CoV-2 increases during zoonotic infection of farmed mink Porter, Ashleigh F Purcell, Damian F J Howden, Benjamin P Duchene, Sebastian Virus Evol Research Article To investigate genetic signatures of adaptation to the mink host, we characterised the evolutionary rate heterogeneity in mink-associated severe acute respiratory syndrome coronaviruses (SARS-CoV-2). In 2020, the first detected anthropozoonotic spillover event of SARS-CoV-2 occurred in mink farms throughout Europe and North America. Both spill-back of mink-associated lineages into the human population and the spread into the surrounding wildlife were reported, highlighting the potential formation of a zoonotic reservoir. Our findings suggest that the evolutionary rate of SARS-CoV-2 underwent an episodic increase upon introduction into the mink host before returning to the normal range observed in humans. Furthermore, SARS-CoV-2 lineages could have circulated in the mink population for a month before detection, and during this period, evolutionary rate estimates were between 3 × 10(–3) and 1.05 × 10(–2) (95 per cent HPD, with a mean rate of 6.59 × 10(–3)) a four- to thirteen-fold increase compared to that in humans. As there is evidence for unique mutational patterns within mink-associated lineages, we explored the emergence of four mink-specific Spike protein amino acid substitutions Y453F, S1147L, F486L, and Q314K. We found that mutation Y453F emerged early in multiple mink outbreaks and that mutations F486L and Q314K may co-occur. We suggest that SARS-CoV-2 undergoes a brief, but considerable, increase in evolutionary rate in response to greater selective pressures during species jumps, which may lead to the occurrence of mink-specific mutations. These findings emphasise the necessity of ongoing surveillance of zoonotic SARS-CoV-2 infections in the future. Oxford University Press 2023-01-10 /pmc/articles/PMC9896948/ /pubmed/36751428 http://dx.doi.org/10.1093/ve/vead002 Text en © The Author(s) 2023. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Porter, Ashleigh F Purcell, Damian F J Howden, Benjamin P Duchene, Sebastian Evolutionary rate of SARS-CoV-2 increases during zoonotic infection of farmed mink |
title | Evolutionary rate of SARS-CoV-2 increases during zoonotic infection of farmed mink |
title_full | Evolutionary rate of SARS-CoV-2 increases during zoonotic infection of farmed mink |
title_fullStr | Evolutionary rate of SARS-CoV-2 increases during zoonotic infection of farmed mink |
title_full_unstemmed | Evolutionary rate of SARS-CoV-2 increases during zoonotic infection of farmed mink |
title_short | Evolutionary rate of SARS-CoV-2 increases during zoonotic infection of farmed mink |
title_sort | evolutionary rate of sars-cov-2 increases during zoonotic infection of farmed mink |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9896948/ https://www.ncbi.nlm.nih.gov/pubmed/36751428 http://dx.doi.org/10.1093/ve/vead002 |
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