Subgenotypes of hepatitis B virus genotype D (D1, D2, D3 and D5) in India: differential pattern of mutations, liver injury and occult HBV infection
Authors: Chandra, P. K.; Biswas, A.1; Datta, S.1; Banerjee, A.; Panigrahi, R.1; Chakrabarti, S.; De, B. K.2; Chakravarty, R.1
Source: Journal of Viral Hepatitis, Volume 16, Number 10, October 2009 , pp. 749-756(8)
Publisher: Wiley-Blackwell
Abstract:
Summary. Hepatitis B genotype D (HBV/D) is the most widespread genotype and exists as at least five subgenotypes (HBV/D1-D5). However, little is known about the association of virological characteristics with clinical differences among HBV/D subgenotypes. To investigate the virological characteristics of these subgenotypes and their clinical implications, we selected a cohort of 109 genotype D infected individuals from the state of West Bengal, India, including 68 HBsAg positive patients and 41 with occult HBV infection. Among the HBsAg positive subjects 28 had chronic hepatitis B virus infection, 40 were asymptomatic carriers based on clinical examination, liver function test and ultrasonograph results. Overall, HBV/D1 was found in 17%, HBV/D2 in 29%, HBV/D3 in 34% and HBV/D5 in 20% of the cases. HBV/D1 was significantly associated with chronic liver disease (P = 0.01), and in this subgenotype A1896 (PreC mutations) were most common. Although BCP mutations (A/C1753 and T1762/A1764) were found to be frequently associated with HBV/D2 (33% and 33%) and D5 (47% and 59%), no apparent clinical correlation was observed. On the other hand, occult HBV infection was significantly associated with HBV/D3 infection, along with low level of BCP and PreC mutations and several non-synonymous substitutions in the catalytic reverse transcriptase (RT) domain of polymerase gene. Similar nucleotide substitutions in the surface (S) gene region were observed from both northern and eastern Indian HBV/D3 isolates. In conclusion, HBV/D subgenotypes differ in their mutational patterns in the S, polymerase and the BCP/PreC regions that may influence their clinical outcomes.Keywords: genetic diversity; genotypes and subgenotypes; HBV mutations; hepatitis B virus; RT domain
Document Type: Research article
DOI: http://dx.doi.org/10.1111/j.1365-2893.2009.01129.x
Affiliations: 1: ICMR Virus Unit, Kolkata 2: Medical College and Hospital, Kolkata, West Bengal, India
Publication date: 2009-10-01
- In this: publication
- By this: publisher
- In this Subject: Gastroenterology
- By this author: Chandra, P. K. ; Biswas, A. ; Datta, S. ; Banerjee, A. ; Panigrahi, R. ; Chakrabarti, S. ; De, B. K. ; Chakravarty, R.

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