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dc.contributor.authorKoyaweda, Giscard W
dc.contributor.authorOngus, Juliette R
dc.contributor.authorMachuka, Eunice
dc.contributor.authorJuma, John
dc.contributor.authorMacharia, Rosaline
dc.contributor.authorKomas, Narcisse P
dc.contributor.authorPelle, Roger
dc.date.accessioned2020-11-02T09:00:02Z
dc.date.available2020-11-02T09:00:02Z
dc.date.issued2020
dc.identifier.citationKoyaweda GW, Ongus JR, Machuka E, Juma J, Macharia R, Komas NP, Pelle R. Detection of circulating hepatitis B virus immune escape and polymerase mutants among HBV-positive patients attending Institut Pasteur de Bangui, Central African Republic. Int J Infect Dis. 2020 Jan;90:138-144. doi: 10.1016/j.ijid.2019.10.039. Epub 2019 Nov 1. PMID: 31682960; PMCID: PMC6912157.en_US
dc.identifier.urihttps://pubmed.ncbi.nlm.nih.gov/31682960/
dc.identifier.urihttp://erepository.uonbi.ac.ke/handle/11295/153251
dc.description.abstractBackground: Previous studies in the Central African Republic (CAR) have reported the presence of hepatitis B virus (HBV) recombinant genotype E/D and a suspicion of immune escape mutants (IEMs), without further investigation into their impact on prevention and diagnosis. Consequently, this study investigated HBV mutations among hepatitis B surface antigen (HBsAg)-positive patients attending Institut Pasteur de Bangui in the CAR. Methods: Sera from a total of 118 HBsAg-positive patients with no previous history of HBV treatment or vaccination at the Institut Pasteur de Bangui, were sampled between 2017 and 2019. Subsequently, the region spanning the surface and polymerase genes of HBV was amplified by PCR and sequenced. HBV sequences were genotyped/subgenotyped by phylogenetic analysis and serotyped based on predicted amino acid residues at positions s122, s127, s140, s159, and s160. They were then analyzed for HBV IEMs and polymerase mutations. Results: The region spanning the surface and polymerase genes was successfully amplified and sequenced for 51 samples. Of the HBV sequences, 49 were genotype E and two were genotype A subgenotype A1; these were serotyped as ayw4 and ayw1, respectively. Potential IEMs sY100C, sA128V, and sM133T, and several polymerase mutants were identified. Conclusions: This study raises awareness of the need for further studies to be conducted on a large scale to better understand HBV mutations for improved disease control and prevention strategies in the country.en_US
dc.language.isoenen_US
dc.publisherUniversity of Nairobien_US
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
dc.subjectCentral African Republic; Genotype/subgenotype; Hepatitis B virus; Immune escape mutants (IEMs); Polymerase mutants; Serotype.en_US
dc.titleDetection of circulating hepatitis B virus immune escape and polymerase mutants among HBV-positive patients attending Institut Pasteur de Bangui, Central African Republicen_US
dc.typeArticleen_US


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