Phylogenetic analysis of new hepatitis B virus isolates from Nigeria supports endemicity of genotype E in West Africa

2001 ◽  
Vol 65 (3) ◽  
pp. 463-469 ◽  
Author(s):  
Solomon O. Odemuyiwa ◽  
Mick N. Mulders ◽  
Oluseyi I. Oyedele ◽  
Samuel O. Ola ◽  
Georgina N. Odaibo ◽  
...  
PLoS ONE ◽  
2014 ◽  
Vol 9 (3) ◽  
pp. e92223 ◽  
Author(s):  
Barbara V. Lago ◽  
Francisco C. Mello ◽  
Flavia S. Ribas ◽  
Fatima Valente ◽  
Caroline C. Soares ◽  
...  

2009 ◽  
Vol 90 (10) ◽  
pp. 2442-2451 ◽  
Author(s):  
Penelope Garmiri ◽  
André Loua ◽  
Nyankoye Haba ◽  
Daniel Candotti ◽  
Jean-Pierre Allain

The prevalence of hepatitis B virus (HBV) surface antigen (HBsAg) chronic carriage in west Africa is the highest in the world, but its molecular epidemiology remains relatively poorly investigated. Plasma samples from random asymptomatic carriers of HBsAg in Conakry, Guinea, were studied and the complete genome sequences of 81 strains were obtained. Three additional samples from Kumasi, Ghana, were also included in the analysis. Phylogenetic analyses confirmed the dominance of genotype E (95.1 %), including 8.6 % of strains (viral load, 5×103–2.6×108 IU ml−1) comprising dominant variants with large deletions in the core region and minority wild-type variants. The presence of two different patterns of deletions in two and four donors suggested targeted genome fragility between nt 1979 and 2314. The remaining sequences included one subgenotype A3 (1 %) and six A/E recombinant forms (4–7 %). A/E strains with identical points of recombination in three donors suggested strongly that these recombinant HBV strains are circulating and transmitted in the population. Recombination points were concentrated in the core gene. The detection of similar A/E recombinant strains in Ghana suggested a geographical extension of recombinant HBV to the region. The quasispecies of one additional Ghanaian strain sequenced in the pre-surface/surface region resolved into dominant clones of either the A or E genotype, but also three different patterns of A/E recombinant variants. The observation that both deletions of genotype E strains and A/E recombination points are mostly located in the core gene at specific positions indicates a region of the genome where genetic rearrangements preferentially take place.


2004 ◽  
Vol 190 (2) ◽  
pp. 400-408 ◽  
Author(s):  
Mick N. Mulders ◽  
Véronique Venard ◽  
Mounjohou Njayou ◽  
A. Patrick Edorh ◽  
Akeeb O. Bola Oyefolu ◽  
...  

2004 ◽  
Vol 75 (2) ◽  
pp. 227-234 ◽  
Author(s):  
Samad Amini-Bavil-Olyaee ◽  
Ramin Sarrami-Forooshani ◽  
Fereidoun Mahboudi ◽  
Farzaneh Sabahi ◽  
Ahmad Adeli ◽  
...  

2005 ◽  
Vol 78 (2) ◽  
pp. 178-184 ◽  
Author(s):  
Tran Thien Tuan Huy ◽  
Koichi Ishikawa ◽  
William Ampofo ◽  
Taku Izumi ◽  
Akira Nakajima ◽  
...  

2006 ◽  
Vol 87 (5) ◽  
pp. 1163-1173 ◽  
Author(s):  
Christophe M. Olinger ◽  
Véronique Venard ◽  
Mounjohou Njayou ◽  
Akeeb O. Bola Oyefolu ◽  
Ibrahim Maïga ◽  
...  

One hundred and twenty-two new hepatitis B virus (HBV) preC/C sequences and three complete genomes from three major countries in West Africa were analysed. The majority of sequences were of genotype E and the only other genotype found was genotype A. Although for genotype E sequences, the genetic diversity of the preC/C gene was about two to three times higher than that of the preS/S gene, it was still considerably lower than that for genotype A sequences. The HBV/E preC/C gene was related most closely to subgenotype D1 and D2 sequences. Evidence of recombination was found in two strains that were of genotype A in the preS/S gene and of genotype E in the preC/C gene. The genotype A strains from Cameroon, Mali and Nigeria could be divided phylogenetically into three subtypes, A3 and two new subtypes, tentatively designated A4 and A5. Each subtype presented a genetic diversity of 2·19–3·85 % and intersubtype distances of 4·47–5·97 %. Interestingly, one sample from Nigeria showed evidence of a triple recombination of genotypes E/D and A, separated by a genotype G-specific insert of 36 bp. Of 110 patients, 19 (17·3 %) showed a coinfection of genotypes A and E, mostly in human immunodeficiency virus-positive children from Cameroon. Thus, in Cameroon, where both genotypes coexist, 37 % of all individuals tested had mixed infections. The low genetic variability in the preC/C gene of genotype E supports our previous speculation about a relatively short evolutionary history of this genotype, in contrast to the subtype-rich African genotype A strains.


2021 ◽  
Author(s):  
Livia Villar ◽  
Barbara Lago ◽  
Cristianne Bezerra ◽  
Ana Mendonça ◽  
Leticia Nabuco ◽  
...  

2005 ◽  
Vol 41 (11) ◽  
pp. 1576-1581 ◽  
Author(s):  
C.-L. Lin ◽  
J.-H. Kao ◽  
B.-F. Chen ◽  
P.-J. Chen ◽  
M.-Y. Lai ◽  
...  

2019 ◽  
Vol 14 (8) ◽  
pp. 509-514
Author(s):  
Giancarlo Ceccarelli ◽  
Eleonora Cella ◽  
Serena Vita ◽  
Alessia Lai ◽  
Erika Ebranati ◽  
...  

A case of hepatitis B virus (HBV) infection in an Eritrean migrant was described to provide an epidemiological approach based on phylogenetic analysis useful in developing countries with lacking information. Migrant, positive for HBsAg and HBeAg, carried HBV at high copy number. A sequence of HBV HBsAg region was used for phylogenetic relationships and genetic variability investigation. In the phylogenetic tree, the sequence corresponded to D2 HBV genotype and the cluster root dated 7 years ago. These data compared with the date of landing in Italy, suggest that he was infected at least 7 years before his arrival. This approach by ‘mirror effect’ allows the reconstruction of HBV epidemiology in the country of origin, analyzing the migrant population in the host country.


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