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Highly Diverse Hepatitis C Strains Detected in Sub‐Saharan Africa Have Unknown Susceptibility to Direct‐Acting Antiviral Treatments

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 i...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6492010/
https://www.ncbi.nlm.nih.gov/pubmed/30387174
http://dx.doi.org/10.1002/hep.30342
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author 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.
author_facet 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.
author_sort Davis, Chris
collection PubMed
description 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.
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spelling pubmed-64920102019-05-06 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. Hepatology Original Articles 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. John Wiley and Sons Inc. 2019-03-22 2019-04 /pmc/articles/PMC6492010/ /pubmed/30387174 http://dx.doi.org/10.1002/hep.30342 Text en © 2018 The Authors. Hepatology published by Wiley Periodicals, Inc. on behalf of American Association for the Study of Liver Diseases. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
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.
Highly Diverse Hepatitis C Strains Detected in Sub‐Saharan Africa Have Unknown Susceptibility to Direct‐Acting Antiviral Treatments
title Highly Diverse Hepatitis C Strains Detected in Sub‐Saharan Africa Have Unknown Susceptibility to Direct‐Acting Antiviral Treatments
title_full Highly Diverse Hepatitis C Strains Detected in Sub‐Saharan Africa Have Unknown Susceptibility to Direct‐Acting Antiviral Treatments
title_fullStr Highly Diverse Hepatitis C Strains Detected in Sub‐Saharan Africa Have Unknown Susceptibility to Direct‐Acting Antiviral Treatments
title_full_unstemmed Highly Diverse Hepatitis C Strains Detected in Sub‐Saharan Africa Have Unknown Susceptibility to Direct‐Acting Antiviral Treatments
title_short Highly Diverse Hepatitis C Strains Detected in Sub‐Saharan Africa Have Unknown Susceptibility to Direct‐Acting Antiviral Treatments
title_sort highly diverse hepatitis c strains detected in sub‐saharan africa have unknown susceptibility to direct‐acting antiviral treatments
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6492010/
https://www.ncbi.nlm.nih.gov/pubmed/30387174
http://dx.doi.org/10.1002/hep.30342
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