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Using host genetics to infer the global spread and evolutionary history of HCV subtype 3a

Using host genetics to infer the global spread and evolutionary history of HCV subtype 3a
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 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.
Evolution, HCV, Host–virus genetics, Phylogenetics, Phylogeography
Lin, Shang-Kuan
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De Maio, Nicola
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Pedergnana, Vincent
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Wu, Chieh-Hsi
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Thézé, Julien
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Wilson, Daniel J
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Barnes, Eleanor
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Ansari, M Azim
6bc3f987-64de-4be7-81c4-bedf1ecb7059
Lin, Shang-Kuan
2e2f6fb9-0bca-429a-896e-50aedd287307
De Maio, Nicola
d675e711-e9b1-4f7f-bc16-b67438373692
Pedergnana, Vincent
84922119-6687-4ab4-a4d2-5dbe6a78652f
Wu, Chieh-Hsi
ace630c6-2095-4ade-b657-241692f6b4d3
Thézé, Julien
08b09d7b-1b76-49a2-8794-759ff6e68a64
Wilson, Daniel J
4aa90f93-d50c-41e1-9988-35e445832ce0
Barnes, Eleanor
2ccdaa43-22ce-4cb1-91ca-2abb35df1966
Ansari, M Azim
6bc3f987-64de-4be7-81c4-bedf1ecb7059

Lin, Shang-Kuan, De Maio, Nicola, Pedergnana, Vincent, Wu, Chieh-Hsi, Thézé, Julien, Wilson, Daniel J, Barnes, Eleanor and Ansari, M Azim (2021) Using host genetics to infer the global spread and evolutionary history of HCV subtype 3a. Virus Evolution, 7 (2), [A1357]. (doi:10.1093/ve/veab065).

Record type: Article

Abstract

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.

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Accepted/In Press date: 8 July 2021
e-pub ahead of print date: 4 August 2021
Additional Information: Funding Information: S.-K.L. was supported by Wellcome Trust (BST00080); J.T. was supported by the European Research Council grant agreement 614725-PATHPHYLODYN; N.D.M. was supported by the European Molecular Biology Laboratory (EMBL); D.J.W. was supported by a Sir Henry Dale Fellowship jointly funded by the Wellcome Trust and the Royal Society (grant number: 101237/Z/13/B) and by the Robertson Foundation; E.B. was supported by the Oxford NIHR Biomedical Research Centre and is an NIHR senior investigator; M.A.A. was supported by a Sir Henry Dale Fellowship jointly funded by the Royal Society and Wellcome Trust (220171/Z/20/Z). Publisher Copyright: © The Author(s) 2021. Published by Oxford University Press.
Keywords: Evolution, HCV, Host–virus genetics, Phylogenetics, Phylogeography

Identifiers

Local EPrints ID: 451025
URI: http://eprints.soton.ac.uk/id/eprint/451025
PURE UUID: e0304210-6bd3-4e01-bf9f-60b1000fcdc6
ORCID for Chieh-Hsi Wu: ORCID iD orcid.org/0000-0001-9386-725X

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Date deposited: 03 Sep 2021 16:31
Last modified: 17 Mar 2024 04:00

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Contributors

Author: Shang-Kuan Lin
Author: Nicola De Maio
Author: Vincent Pedergnana
Author: Chieh-Hsi Wu ORCID iD
Author: Julien Thézé
Author: Daniel J Wilson
Author: Eleanor Barnes
Author: M Azim Ansari

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