Endemic HBV among hospital in-patients in Bangladesh, including evidence of occult infection

Author:

Chowdhury Fazle Rabbi123,McNaughton Anna L.2ORCID,Amin Mohammad Robed4ORCID,Barai Lovely5ORCID,Saha Mili Rani5ORCID,Rahman Tanjila5ORCID,Das Bikash Chandra6ORCID,Hasan M. Rokibul5,Islam K. M. Shahidul5ORCID,Faiz M. A.7,Al-Mahtab Mamun8,Mokaya Jolynne2ORCID,Kronsteiner Barbara92ORCID,Jeffery Katie10,Andersson Monique I.10,de Cesare Mariateresa11ORCID,Ansari M. Azim112ORCID,Dunachie Susanna92110ORCID,Matthews Philippa C.10122

Affiliation:

1. Mahidol-Oxford Tropical Medicine Research Unit (MORU), Bangkok 10400, Thailand

2. Nuffield Department of Medicine, Peter Medawar Building for Pathogen Research, South Parks Rd, Oxford OX1 3SY, UK

3. Department of Internal Medicine, Bangabandhu Sheikh Mujib Medical University, Dhaka 1200, Bangladesh

4. Department of Medicine, Dhaka Medical College, Dhaka 1200, Bangladesh

5. Department of Microbiology, BIRDEM General Hospital, Dhaka 1200, Bangladesh

6. Surveillance and Immunization Unit, World Health Organization Office, Dhaka 1200, Bangladesh

7. Dev Care Foundation, Dhaka 1200, Bangladesh

8. Department of Hepatology, Bangabandhu Sheikh Mujib Medical University, Dhaka 1200, Bangladesh

9. Centre for Tropical Medicine and Global Health, Peter Medawar Building for Pathogen Research, South Parks Road, Oxford, OX1 3SY, UK

10. Department of Microbiology and Infectious Diseases, Oxford University Hospitals NHS Foundation Trust, John Radcliffe Hospital, Headley Way, Headington, Oxford OX1 3SY, UK

11. Wellcome Centre for Human Genetics, Roosevelt Drive, Headington, Oxford, OX3 7BN, UK

12. NIHR Biomedical Research Centre, John Radcliffe Hospital, Headley Way, Headington, Oxford OX1 3SY, UK

Abstract

Bangladesh is one of the top-ten most heavily burdened countries for viral hepatitis, with hepatitis B (HBV) infections responsible for the majority of cases. Recombinant and occult HBV infections (OBI) have been reported previously in the region. We investigated an adult fever cohort (n=201) recruited in Dhaka, to determine the prevalence of HBV and OBI. A target-enrichment deep sequencing pipeline was applied to samples with HBV DNA >3.0 log10 IU ml−1. HBV infection was present in 16/201 (8 %), among whom 3/16 (19 %) were defined as OBI (HBsAg-negative but detectable HBV DNA). Whole genome deep sequences (WGS) were obtained for four cases, identifying genotypes A, C and D. One OBI case had sufficient DNA for sequencing, revealing multiple polymorphisms in the surface gene that may contribute to the occult phenotype. We identified mutations associated with nucleos(t)ide analogue resistance in 3/4 samples sequenced, although the clinical significance in this cohort is unknown. The high prevalence of HBV in this setting illustrates the importance of opportunistic clinical screening and DNA testing of transfusion products to minimise OBI transmission. WGS can inform understanding of diverse disease phenotypes, supporting progress towards international targets for HBV elimination.

Funder

Commonwealth

Wellcome Trust

National Institute for Health Research

Publisher

Microbiology Society

Subject

Virology

Reference54 articles.

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