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

Author:

Lin Shang-Kuan1ORCID,De Maio Nicola2ORCID,Pedergnana Vincent3,Wu Chieh-Hsi4,Thézé Julien56,Wilson Daniel J1ORCID,Barnes Eleanor7,Ansari M Azim17

Affiliation:

1. Nuffield Department of Population Health, Big Data Institute, University of Oxford, Li Ka Shing Centre for Health Information and Discovery, Old Road Campus, Oxford OX3 7LF, UK

2. European Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Wellcome Genome Campus, Hinxton CB10 1SD, UK

3. MIVEGEC, Université de Montpellier, CNRS, 911 avenue Agropolis, Montpellier 34000, France

4. Building 54, Mathematical Sciences University of Southampton, Highfield, Southampton SO17 1BJ, UK

5. Department of Zoology, University of Oxford, South Parks Road, Oxford, Oxfordshire OX1 3PS, UK

6. Université Clermont Auvergne, INRAE, VetAgro Sup, UMR EPIA, Centre INRAE Clermont-Auvergne-Rhône-Alpes, Saint-Genès-Champanelle 63122, France

7. Peter Medawar Building for Pathogen Research, University of Oxford, South Parks Road, Oxford, Oxfordshire OX1 3SY, UK

Abstract

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.

Funder

Joint funding of Wellcome Trust and the Royal Society

Wellcome Trust

Robertson Foundation

H2020 European Research Council

Medical Research Council

Publisher

Oxford University Press (OUP)

Subject

Virology,Microbiology

Reference53 articles.

1. A Global Reference for Human Genetic Variation;The 1000 Genomes Project Consortium;Nature,2015

2. Genome-to-Genome Analysis Highlights the Impact of the Human Innate and Adaptive Immune Systems on the Hepatitis C Virus;Ansari;Nature Genetics,2017

3. Interferon Lambda 4 Impacts the Genetic Diversity of Hepatitis C Virus;eLife,2019

4. BEAST 2: A Software Platform for Bayesian Evolutionary Analysis;Bouckaert;PLoS Computational Biology,2014

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