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Using host genetics to infer the global spread and evolutionary history of HCV subtype 3a
Studies have shown that hepatitis C virus subtype 3a (HCV-3a) is likely to have been circulating in South Asia before its global spread. However, the time and route of this dissemination remain unclear. For the first time, we generated host and virus genome-wide data for more than 500 patients infec...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8438900/ https://www.ncbi.nlm.nih.gov/pubmed/34532064 http://dx.doi.org/10.1093/ve/veab065 |
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author | Lin, Shang-Kuan De Maio, Nicola Pedergnana, Vincent Wu, Chieh-Hsi Thézé, Julien Wilson, Daniel J Barnes, Eleanor Ansari, M Azim |
author_facet | Lin, Shang-Kuan De Maio, Nicola Pedergnana, Vincent Wu, Chieh-Hsi Thézé, Julien Wilson, Daniel J Barnes, Eleanor Ansari, M Azim |
author_sort | Lin, Shang-Kuan |
collection | PubMed |
description | Studies have shown that hepatitis C virus subtype 3a (HCV-3a) is likely to have been circulating in South Asia before its global spread. However, the time and route of this dissemination remain unclear. For the first time, we generated host and virus genome-wide data for more than 500 patients infected with HCV-3a from the UK, North America, Australia, and New Zealand. We used the host genomic data to infer the ancestry of the patients and used this information to investigate the epidemic history of HCV-3a. We observed that viruses from hosts of South Asian ancestry clustered together near the root of the tree, irrespective of the sampling country, and that they were more diverse than viruses from other host ancestries. We hypothesized that South Asian hosts are more likely to have been infected in South Asia and used the inferred host ancestries to distinguish between the location where the infection was acquired and where the sample was taken. Next, we inferred that three independent transmission events resulted in the spread of the virus from South Asia to the UK, North America, and Oceania. This initial spread happened during or soon after the end of World War II. This was subsequently followed by many independent transmissions between the UK, North America, and Oceania. Using both host and virus genomic information can be highly informative in studying the virus epidemic history, especially in the context of chronic infections where migration histories need to be accounted for. |
format | Online Article Text |
id | pubmed-8438900 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-84389002021-09-15 Using host genetics to infer the global spread and evolutionary history of HCV subtype 3a Lin, Shang-Kuan De Maio, Nicola Pedergnana, Vincent Wu, Chieh-Hsi Thézé, Julien Wilson, Daniel J Barnes, Eleanor Ansari, M Azim Virus Evol Research Article Studies have shown that hepatitis C virus subtype 3a (HCV-3a) is likely to have been circulating in South Asia before its global spread. However, the time and route of this dissemination remain unclear. For the first time, we generated host and virus genome-wide data for more than 500 patients infected with HCV-3a from the UK, North America, Australia, and New Zealand. We used the host genomic data to infer the ancestry of the patients and used this information to investigate the epidemic history of HCV-3a. We observed that viruses from hosts of South Asian ancestry clustered together near the root of the tree, irrespective of the sampling country, and that they were more diverse than viruses from other host ancestries. We hypothesized that South Asian hosts are more likely to have been infected in South Asia and used the inferred host ancestries to distinguish between the location where the infection was acquired and where the sample was taken. Next, we inferred that three independent transmission events resulted in the spread of the virus from South Asia to the UK, North America, and Oceania. This initial spread happened during or soon after the end of World War II. This was subsequently followed by many independent transmissions between the UK, North America, and Oceania. Using both host and virus genomic information can be highly informative in studying the virus epidemic history, especially in the context of chronic infections where migration histories need to be accounted for. Oxford University Press 2021-07-09 /pmc/articles/PMC8438900/ /pubmed/34532064 http://dx.doi.org/10.1093/ve/veab065 Text en © The Author(s) 2021. 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 (http://creativecommons.org/licenses/by/4.0/ (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 Lin, Shang-Kuan De Maio, Nicola Pedergnana, Vincent Wu, Chieh-Hsi Thézé, Julien Wilson, Daniel J Barnes, Eleanor Ansari, M Azim Using host genetics to infer the global spread and evolutionary history of HCV subtype 3a |
title | Using host genetics to infer the global spread and evolutionary history of HCV subtype 3a |
title_full | Using host genetics to infer the global spread and evolutionary history of HCV subtype 3a |
title_fullStr | Using host genetics to infer the global spread and evolutionary history of HCV subtype 3a |
title_full_unstemmed | Using host genetics to infer the global spread and evolutionary history of HCV subtype 3a |
title_short | Using host genetics to infer the global spread and evolutionary history of HCV subtype 3a |
title_sort | using host genetics to infer the global spread and evolutionary history of hcv subtype 3a |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8438900/ https://www.ncbi.nlm.nih.gov/pubmed/34532064 http://dx.doi.org/10.1093/ve/veab065 |
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