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Highly Diverse Hepatitis C Strains Detected in Sub-Saharan Africa Have Unknown Susceptibility to Direct-Acting Antiviral Treatments.
Davis, Chris; Mgomella, George S; da Silva Filipe, Ana; Frost, Eric H; Giroux, Genevieve; Hughes, Joseph; Hogan, Catherine; Kaleebu, Pontiano; Asiki, Gershim; McLauchlan, John; Niebel, Marc; Ocama, Ponsiano; Pomila, Cristina; Pybus, Oliver G; Pépin, Jacques; Simmonds, Peter; Singer, Joshua B; Sreenu, Vattipally B; Wekesa, Clara; Young, Elizabeth H; Murphy, Donald G; Sandhu, Manj; Thomson, Emma C.
Affiliation
  • Davis C; Medical Research Council - University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.
  • Mgomella GS; Department of Medicine - University of Cambridge, Cambridge, Cambridgeshire, United Kingdom.
  • da Silva Filipe A; Wellcome Sanger Institute, Hinxton, Cambridgeshire, United Kingdom.
  • Frost EH; Medical Research Council - University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.
  • Giroux G; University of Sherbrooke, Sherbrooke, Quebec, Canada.
  • Hughes J; University of Sherbrooke, Sherbrooke, Quebec, Canada.
  • Hogan C; Medical Research Council - University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.
  • Kaleebu P; University of Sherbrooke, Sherbrooke, Quebec, Canada.
  • Asiki G; Medical Research Council/Uganda Virus Research Institute & London School of Hygiene and Tropical Medicine Uganda Research Unit, Entebbe, Uganda.
  • McLauchlan J; Uganda Virus Research Institute, Entebbe, Uganda.
  • Niebel M; Uganda Virus Research Institute, Entebbe, Uganda.
  • Ocama P; Medical Research Council - University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.
  • Pomila C; Medical Research Council - University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.
  • Pybus OG; Department of Medicine, Makerere University College of Health Sciences, Kampala, Uganda.
  • Pépin J; Department of Medicine - University of Cambridge, Cambridge, Cambridgeshire, United Kingdom.
  • Simmonds P; Department of Zoology, University of Oxford, Oxford, United Kingdom.
  • Singer JB; University of Sherbrooke, Sherbrooke, Quebec, Canada.
  • Sreenu VB; Peter Medawar Building for Pathogen Research, University of Oxford, United Kingdom.
  • Wekesa C; Medical Research Council - University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.
  • Young EH; Medical Research Council - University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.
  • Murphy DG; Uganda Virus Research Institute, Entebbe, Uganda.
  • Sandhu M; Department of Medicine - University of Cambridge, Cambridge, Cambridgeshire, United Kingdom.
  • Thomson EC; Wellcome Sanger Institute, Hinxton, Cambridgeshire, United Kingdom.
Hepatology ; 69(4): 1426-1441, 2019 04.
Article in En | MEDLINE | ID: mdl-30387174
ABSTRACT
The global plan to eradicate hepatitis C virus (HCV) led by the World Health Organization outlines the use of highly effective direct-acting antiviral drugs (DAAs) to achieve elimination by 2030. Identifying individuals with active disease and investigation of the breadth of diversity of the virus in sub-Saharan Africa (SSA) is essential as genotypes in this region (where very few clinical trials have been carried out) are distinct from those found in other parts of the world. We undertook a population-based, nested case-control study in Uganda and obtained additional samples from the Democratic Republic of Congo (DRC) to estimate the prevalence of HCV, assess strategies for disease detection using serological and molecular techniques, and characterize genetic diversity of the virus. Using next-generation and Sanger sequencing, we aimed to identify strains circulating in East and Central Africa. A total of 7,751 Ugandan patients were initially screened for HCV, and 20 PCR-positive samples were obtained for sequencing. Serological assays were found to vary significantly in specificity for HCV. HCV strains detected in Uganda included genotype (g) 4k, g4p, g4q, and g4s and a newly identified unassigned g7 HCV strain. Two additional unassigned g7 strains were identified in patients originating from DRC (one partial and one full open reading frame sequence). These g4 and g7 strains contain nonstructural (ns) protein 3 and 5A polymorphisms associated with resistance to DAAs in other genotypes. Clinical studies are therefore indicated to investigate treatment response in infected patients.

Conclusion:

Although HCV prevalence and genotypes have been well characterized in patients in well-resourced countries, clinical trials are urgently required in SSA, where highly diverse g4 and g7 strains circulate.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hepatitis C / Hepacivirus / Drug Resistance, Viral Type of study: Clinical_trials / Observational_studies / Prevalence_studies / Risk_factors_studies Limits: Aged / Aged80 / Female / Humans / Male / Middle aged Country/Region as subject: Africa Language: En Journal: Hepatology Year: 2019 Document type: Article Affiliation country: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hepatitis C / Hepacivirus / Drug Resistance, Viral Type of study: Clinical_trials / Observational_studies / Prevalence_studies / Risk_factors_studies Limits: Aged / Aged80 / Female / Humans / Male / Middle aged Country/Region as subject: Africa Language: En Journal: Hepatology Year: 2019 Document type: Article Affiliation country: United kingdom