Characterization of the Occult Hepatitis B Virus Variants Circulating among the Blood Donors from Eastern India

Author:

Biswas Avik1,Panigrahi Rajesh12ORCID,Chandra Partha Kumar12,Banerjee Arup13,Datta Sibnarayan14ORCID,Pal Manisha5ORCID,Chakraborty Subhashish6,Bhattacharya Prasun7,Chakrabarti Sekhar8,Chakravarty Runu1

Affiliation:

1. ICMR Virus Unit, Kolkata, GB 4, 1st Floor, ID & BG Hospital Campus, 57 Dr. Suresh Chandra Banerjee Road, Kolkata 700010, India

2. Tulane University Health Sciences Center, Department of Pathology and Laboratory Medicine, 1430 Tulane Avenue SL-79, New Orleans, LA 70112-2699, USA

3. Translational Health Science and Technology Institute (THSTI), Gurgaon, Haryana 122016, India

4. Defence Research Laboratory, Tezpur, Assam 784001, India

5. Department of Statistics, University of Calcutta, Kolkata 700019, India

6. Institute of Blood Transfusion Medicine and Immunohematology, Kolkata 700006, India

7. Medical College & Hospital, Kolkata 700073, West Bengal, India

8. National Institute of Cholera and Enteric Diseases, Kolkata 700010, India

Abstract

A previous study from West Bengal documented very high rate of occult HBV infection (OBI) among the HBsAg negative blood donors. This study was aimed to characterize the OBI strains circulating among the blood donors and to estimate the risk associated with the prevailing viral variants/mutants. Blood samples from 2195 voluntary blood donors were included in the study. HBsAg, HBeAg, anti-HBc, and anti-HBs statuses of the samples were done by ELISA based detection. PCR amplification and sequencing were done to determine HBV genotypes, basal core promoter (BCP), and precore (Pre-C) mutations. Among the study samples, 268 were anti-HBc positive/HBsAg negative, among which 65 (24.25%) were HBV DNA positive. Phylogenetic analysis revealed the presence of HBV/D (87.23%), HBV/A (8.51%), and HBV/C (4.26%) (P<0.0001).HBV/D3 (65.85%) was the significantly prevalent subgenotype over HBV/D2 (26.83%) and HBV/D1 (7.31%) (P=0.0003). Considerable prevalence of differential BCP (1752C, 1753C, 1762T/1764A, 1753C+1762T/1764A, 1773C, and 1814C) and reverse transcriptase (rt) gene (rtI91L, rtL93P, rtS106C, rtR110G, rtN118T, rtS119T, rtY126H, rtG127W/R, rtC136R, and rtY158H) mutations was identified. Association of specific HBV subgenotypes with OBI was interesting and needs further study. Clinically relevant mutations were prevalent among the OBI strains which are of serious concern.

Funder

West Bengal State AIDS Prevention and Control Society

Publisher

Hindawi Limited

Subject

General Environmental Science,General Biochemistry, Genetics and Molecular Biology,General Medicine

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