Eight novel hepatitis C virus genomes reveal the changing taxonomic structure of genotype 6

Author:

Wang Hongren1,Yuan Zhiguo1,Barnes Eleanor2,Yuan Manqiong3,Li Chunhua3,Fu Yongshui4,Xia Xueshan5,Li Gang1,Newton Paul N.678,Vongsouvath Manivanh6,Klenerman Paul2,Pybus Oliver G.9,Murphy Donald10,Abe Kenji10,Lu Ling3

Affiliation:

1. Vaccine Institute, 3rd Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong, PR China

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

3. The Viral Oncology Center, Department of Pathology and Laboratory Medicine, University of Kansas Medical Center, Kansas City, Kansas, USA

4. Guangzhou Blood Center, Guangzhou, Guangdong, PR China

5. Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, Yunnan, PR China

6. Wellcome Trust-Mahosot Hospital-Oxford Tropical Medicine Research Collaboration, Microbiology Laboratory, Mahosot Hospital, Vientiane, Lao PDR

7. Centre for Clinical Vaccinology and Tropical Medicine, Churchill Hospital, Nuffield Department of Medicine, University of Oxford, Oxford OX3 7LJ, UK

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

9. Institut National de Santé Publique du Québec, Laboratoire de Santé Publique du Québec, Sainte-Anne-de-Bellevue, QC, Canada

10. Department of Pathology, National Institute of Infectious Diseases, Shinjuku-ku, Tokyo 162-8640, Japan

Abstract

Analysis of partial hepatitis C virus sequences has revealed many novel genotype 6 variants that cannot be unambiguously classified, which obscure the distinctiveness of pre-existing subtypes. To explore this uncertainty, we obtained genomes of 98.0–98.8 % full-length for eight such variants (KM35, QC273, TV257, TV476, TV533, L349, QC271 and DH027) and characterized them using phylogenetic analyses and per cent nucleotide similarities. The former four are closely related phylogenetically to subtype 6k, TV533 and L349 to subtype 6l, QC271 to subtypes 6i and 6j, and DH027 to subtypes 6m and 6n. The former six defined a high-level grouping that comprised subtypes 6k and 6l, plus related strains. The threshold between intra- and inter-subtype diversity in this group was indistinct. We propose that similar results would be seen elsewhere if more intermediate variants like QC271 and DH027 were sampled.

Publisher

Microbiology Society

Subject

Virology

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