Phylogenetic Analysis of Hepatitis C Virus Infections in a Large Belgian Cohort Using Next-Generation Sequencing of Full-Length Genomes

Author:

Christensen Kasper T.1,Pierard Florian1,Bonsall David23,Bowden Rory3,Barnes Eleanor456,Florence Eric78,Ansari M. Azim9,Nguyen Dung3,de Cesare Mariateresa3,Nevens Frederik10,Robaeys Geert101112,Schrooten Yoeri113,Busschots Dana1112ORCID,Simmonds Peter14ORCID,Vandamme Anne-Mieke115ORCID,Van Wijngaerden Eric16,Dierckx Tim1ORCID,Cuypers Lize11317ORCID,Van Laethem Kristel113ORCID

Affiliation:

1. Laboratory of Clinical and Epidemiological Virology, Department of Microbiology, Immunology and Transplantation, Rega Institute for Medical Research, KU Leuven, 3000 Leuven, Belgium

2. Big Data Institute, Li Ka Shing Centre for Health Information and Discovery, Nuffield Department of Medicine, University of Oxford, Oxford OX3 7LF, UK

3. The Wellcome Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford OX3 7BN, UK

4. Peter Medawar Building for Pathogen Research, University of Oxford, Oxford OX1 3SY, UK

5. Translational Gastroenterology Unit, University of Oxford, Oxford OX3 9DU, UK

6. Oxford NIHR Biomedical Research Centre, University of Oxford, Oxford OX3 9DU, UK

7. Department of General Internal Medicine, Infectious Diseases and Tropical Medicine, Antwerp University Hospital, 2650 Edegem, Belgium

8. Department of Clinical Sciences, Institute of Tropical Medicine, 2000 Antwerp, Belgium

9. Nuffield Department of Medicine, University of Oxford, Oxford OX3 7BN, UK

10. Department of Gastroenterology and Hepatology, University Hospitals Leuven, 3000 Leuven, Belgium

11. Faculty of Medicine and Life Sciences—LCRC, UHasselt, Agoralaan, 3590 Diepenbeek, Belgium

12. Department of Gastroenterology and Hepatology, Ziekenhuis Oost-Limburg, 3600 Genk, Belgium

13. Department of Laboratory Medicine, University Hospitals Leuven, 3000 Leuven, Belgium

14. Henry Wellcome Building for Molecular Physiology, Nuffield Department of Medicine, University of Oxford, Old Road Campus, Headington, Oxford OX3 7BN, UK

15. Global Health and Tropical Medicine, Institute of Hygiene and Tropical Medicine, Universidade Nova de Lisboa, Rua da Junqueira 100, 1349-008 Lisbon, Portugal

16. Department of General Internal Medicine, University Hospitals Leuven, 3000 Leuven, Belgium

17. Laboratory of Clinical Microbiology, Department of Microbiology, Immunology and Transplantation, KU Leuven, 3000 Leuven, Belgium

Abstract

The hepatitis C virus (HCV) epidemic in Western countries is primarily perpetuated by the sub-populations of men who have sex with men (MSM) and people who inject drugs (PWID). Understanding the dynamics of transmission in these communities is crucial for removing the remaining hurdles towards HCV elimination. We sequenced 269 annotated HCV plasma samples using probe enrichment and next-generation sequencing, obtaining 224 open reading frames of HCV (OR497849-OR498072). Maximum likelihood phylogenies were generated on the four most prevalent subtypes in this study (HCV1a, 1b, 3a, 4d) with a subsequent transmission cluster analysis. The highest rate of clustering was observed for HCV4d samples (13/17 (76.47%)). The second highest rate of clustering was observed in HCV1a samples (42/78 (53.85%)) with significant association with HIV-positive MSM. HCV1b and HCV3a had very low rates of clustering (2/83 (2.41%) and (0/29)). The spread of the prevalent subtype HCV1b appears to have been largely curtailed, and we demonstrate the onwards transmission of HCV1a and HCV4d in the HIV-positive MSM population across municipal borders. More systematic data collection and sequencing is needed to allow a better understanding of the HCV transmission among the community of PWID and overcome the remaining barriers for HCV elimination in Belgium.

Funder

Fonds Wetenschappelijk Onderzoek Vlaanderen

FWO travel grant

Wellcome Trust

Medical Research Council

Publisher

MDPI AG

Subject

Virology,Infectious Diseases

Reference63 articles.

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