Novel porcine-like human G26P[19] rotavirus identified in hospitalized paediatric diarrhoea patients in Ho Chi Minh City, Vietnam

Author:

My Phan Vu Tra12,Rabaa Maia A.32,Donato Celeste45,Cowley Daniel5,Phat Voong Vinh2,Dung Tran Thi Ngoc2,Anh Pham Hong2,Vinh Ha6,Bryant Juliet E.7,Kellam Paul81,Thwaites Guy92,Woolhouse Mark E. J.3,Kirkwood Carl D.45,Baker Stephen1092

Affiliation:

1. The Wellcome Trust Sanger Institute, Hinxton, Cambridge, UK

2. The Hospital for Tropical Diseases, Wellcome Trust Major Overseas Programme, Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam

3. Centre for Immunity, Infection and Evolution, University of Edinburgh, Edinburgh, UK

4. La Trobe University, Melbourne, Australia

5. Murdoch Childrens Research Institute, Melbourne, Australia

6. The Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam

7. Wellcome Trust Major Overseas Programme, Oxford University Clinical Research Unit, Hanoi, Vietnam

8. Division of Infection and Immunity, University College London, London, United Kingdom

9. Centre for Tropical Medicine, Nuffield Department of Clinical Medicine, Oxford University, Oxford, UK

10. The London School of Hygiene and Tropical Medicine, London, UK

Abstract

During a hospital-based diarrhoeal disease study conducted in Ho Chi Minh City, Vietnam from 2009 to 2010, we identified four symptomatic children infected with G26P[19] rotavirus (RV) – an atypical variant that has not previously been reported in human gastroenteritis. To determine the genetic structure and investigate the origin of this G26P[19] strain, the whole genome of a representative example was characterized, revealing a novel genome constellation: G26–P[19]–I5–R1–C1–M1–A8–N1–T1–E1–H1. The genome segments were most closely related to porcine (VP7, VP4, VP6 and NSP1) and Wa-like porcine RVs (VP1–3 and NSP2–5). We proposed that this G26P[19] strain was the product of zoonotic transmission coupled with one or more reassortment events occurring in human and/or animal reservoirs. The identification of such strains has potential implications for vaccine efficacy in south-east Asia, and outlines the utility of whole-genome sequencing for studying RV diversity and zoonotic potential during disease surveillance.

Publisher

Microbiology Society

Subject

Virology

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