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Detection of circulating hepatitis B virus immune escape and polymerase mutants among HBV-positive patients attending Institut Pasteur de Bangui, Central African Republic.
Koyaweda, Giscard Wilfried; Ongus, Juliette Rose; Machuka, Eunice; Juma, John; Macharia, Rosaline; Komas, Narcisse Patrice; Pelle, Roger.
Afiliação
  • Koyaweda GW; Pan African University, Institute for Basic Sciences Technology and Innovation, Nairobi, Kenya.
  • Ongus JR; Jomo Kenyatta University of Agriculture and Technology, Medical Laboratory Sciences Department, Nairobi, Kenya.
  • Machuka E; Biosciences eastern and central Africa International Livestock Research Institute (BecA-ILRI) Hub, Nairobi, Kenya.
  • Juma J; Biosciences eastern and central Africa International Livestock Research Institute (BecA-ILRI) Hub, Nairobi, Kenya.
  • Macharia R; Center for Biotechnology and Bioinformatics, University of Nairobi, Nairobi, Kenya.
  • Komas NP; Institut Pasteur de Bangui, Viral Hepatitis Laboratory, Bangui, Central African Republic.
  • Pelle R; Jomo Kenyatta University of Agriculture and Technology, Medical Laboratory Sciences Department, Nairobi, Kenya. Electronic address: r.pelle@cgiar.org.
Int J Infect Dis ; 90: 138-144, 2020 Jan.
Article em En | MEDLINE | ID: mdl-31682960
ABSTRACT

BACKGROUND:

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.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 2_ODS3 Base de dados: MEDLINE Assunto principal: Proteínas Virais / Vírus da Hepatite B / DNA Polimerase Dirigida por DNA / Hepatite B Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adolescent / Adult / Female / Humans / Male / Middle aged País/Região como assunto: Africa Idioma: En Revista: Int J Infect Dis Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 2_ODS3 Base de dados: MEDLINE Assunto principal: Proteínas Virais / Vírus da Hepatite B / DNA Polimerase Dirigida por DNA / Hepatite B Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adolescent / Adult / Female / Humans / Male / Middle aged País/Região como assunto: Africa Idioma: En Revista: Int J Infect Dis Ano de publicação: 2020 Tipo de documento: Article