Molecular analysis of HBV genotypes and subgenotypes in the Central-East region of Tunisia

<p>Abstract</p> <p>Background</p> <p>In Tunisia, country of intermediate endemicity for Hepatitis B virus (HBV) infection, most molecular studies on the virus have been carried out in the North of the country and little is known about other regions. The aim of this stud...

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Main Authors: Gharbi Jawhar, Ferjani Asma, Thibault Vincent, Bahri Olfa, Fredj Nadia, Hannachi Naila, Triki Henda, Boukadida Jalel
Format: Article
Language:English
Published: BMC 2010-11-01
Series:Virology Journal
Online Access:http://www.virologyj.com/content/7/1/302
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spelling doaj-8c8942a0eb47466f967c0bb0c33c79702020-11-24T21:14:32ZengBMCVirology Journal1743-422X2010-11-017130210.1186/1743-422X-7-302Molecular analysis of HBV genotypes and subgenotypes in the Central-East region of TunisiaGharbi JawharFerjani AsmaThibault VincentBahri OlfaFredj NadiaHannachi NailaTriki HendaBoukadida Jalel<p>Abstract</p> <p>Background</p> <p>In Tunisia, country of intermediate endemicity for Hepatitis B virus (HBV) infection, most molecular studies on the virus have been carried out in the North of the country and little is known about other regions. The aim of this study was to determine HBV genotype and subgenotypes in Central-East Tunisia. A total of 217 HBs antigen positive patients were enrolled and determination of genotype was investigated in 130 patients with detectable HBV DNA. HBV genotyping methods were: PCR-RFLP on the pre-S region, a PCR using type-specific primers in the S region (TSP-PCR) and partial sequencing in the pre-S region.</p> <p>Results</p> <p>Three genotypes (D, B and A) were detected by the PCR-RFLP method and two (D and A) with the TSP-PCR method, the concordance between the two methods was 93%. Sequencing and phylogenetic analysis of 32 strains, retrieved the same genotype (D and A) for samples with concordant results and genotype D for samples with discordant results. The sequences of discordant genotypes had a restriction site in the pre-S gene which led to erroneous result by the PCR-RFLP method. Thus, prevalence of genotype D and A was 96% and 4%, respectively. Phylogenetic analysis showed the predominance of two subgenotypes D1 (55%) and D7 (41%). Only one strain clustered with D3 subgenotype (3%).</p> <p>Conclusions</p> <p>Predominance of subgenotype D7 appears to occur in northern regions of Africa with transition to subgenotype D1 in the East of the continent. HBV genetic variability may lead to wrong results in rapid genotyping methods and sequence analysis is needed to clarify atypical results.</p> http://www.virologyj.com/content/7/1/302
collection DOAJ
language English
format Article
sources DOAJ
author Gharbi Jawhar
Ferjani Asma
Thibault Vincent
Bahri Olfa
Fredj Nadia
Hannachi Naila
Triki Henda
Boukadida Jalel
spellingShingle Gharbi Jawhar
Ferjani Asma
Thibault Vincent
Bahri Olfa
Fredj Nadia
Hannachi Naila
Triki Henda
Boukadida Jalel
Molecular analysis of HBV genotypes and subgenotypes in the Central-East region of Tunisia
Virology Journal
author_facet Gharbi Jawhar
Ferjani Asma
Thibault Vincent
Bahri Olfa
Fredj Nadia
Hannachi Naila
Triki Henda
Boukadida Jalel
author_sort Gharbi Jawhar
title Molecular analysis of HBV genotypes and subgenotypes in the Central-East region of Tunisia
title_short Molecular analysis of HBV genotypes and subgenotypes in the Central-East region of Tunisia
title_full Molecular analysis of HBV genotypes and subgenotypes in the Central-East region of Tunisia
title_fullStr Molecular analysis of HBV genotypes and subgenotypes in the Central-East region of Tunisia
title_full_unstemmed Molecular analysis of HBV genotypes and subgenotypes in the Central-East region of Tunisia
title_sort molecular analysis of hbv genotypes and subgenotypes in the central-east region of tunisia
publisher BMC
series Virology Journal
issn 1743-422X
publishDate 2010-11-01
description <p>Abstract</p> <p>Background</p> <p>In Tunisia, country of intermediate endemicity for Hepatitis B virus (HBV) infection, most molecular studies on the virus have been carried out in the North of the country and little is known about other regions. The aim of this study was to determine HBV genotype and subgenotypes in Central-East Tunisia. A total of 217 HBs antigen positive patients were enrolled and determination of genotype was investigated in 130 patients with detectable HBV DNA. HBV genotyping methods were: PCR-RFLP on the pre-S region, a PCR using type-specific primers in the S region (TSP-PCR) and partial sequencing in the pre-S region.</p> <p>Results</p> <p>Three genotypes (D, B and A) were detected by the PCR-RFLP method and two (D and A) with the TSP-PCR method, the concordance between the two methods was 93%. Sequencing and phylogenetic analysis of 32 strains, retrieved the same genotype (D and A) for samples with concordant results and genotype D for samples with discordant results. The sequences of discordant genotypes had a restriction site in the pre-S gene which led to erroneous result by the PCR-RFLP method. Thus, prevalence of genotype D and A was 96% and 4%, respectively. Phylogenetic analysis showed the predominance of two subgenotypes D1 (55%) and D7 (41%). Only one strain clustered with D3 subgenotype (3%).</p> <p>Conclusions</p> <p>Predominance of subgenotype D7 appears to occur in northern regions of Africa with transition to subgenotype D1 in the East of the continent. HBV genetic variability may lead to wrong results in rapid genotyping methods and sequence analysis is needed to clarify atypical results.</p>
url http://www.virologyj.com/content/7/1/302
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