Hepatitis C Virus Genetic Diversity and Drug Mutational Analysis in Cameroon: 1992 to 2013

Judith Ndongo Torimiro *

Faculty of Medicine and Biomedical Sciences, University of Yaounde I, Cameroon and Centre International de Référence Chantal Biya pour la Recherche sur la Prévention et de la Prise en Charge du VIH/SIDA (CIRCB), Cameroon

Laure Arlette Tchapda

Centre International de Référence Chantal Biya pour la Recherche sur la Prévention et de la Prise en Charge du VIH/SIDA (CIRCB), Cameroon and Department of Biochemistry, Faculty of Science, University of Yaounde I, Cameroon

Maurice Boda

Microbiology Laboratory, Faculty of Science, University of Yaounde I, Cameroon

Jude Saber Bimela

Centre International de Référence Chantal Biya pour la Recherche sur la Prévention et de la Prise en Charge du VIH/SIDA (CIRCB), Cameroon and Hepatitis Center, Johns Hopkins School of Medicine, Johns Hopkins University, USA

Dale Netski

Hepatitis Center, Johns Hopkins School of Medicine, Johns Hopkins University, USA

Désire Takou

Centre International de Référence Chantal Biya pour la Recherche sur la Prévention et de la Prise en Charge du VIH/SIDA (CIRCB), Cameroon

Donald Scot Burke

University of Pittsburg Graduate School of Public Health, USA

Ubald Tamoufe

Global Virus Cameroon, Yaounde, Cameroon

Eitel Mpoudi-Ngole

CREMER, Institut Médicale des Plantes Médicinal, Cameroon

Henry Namme Luma

Faculty of Medicine and Biomedical Sciences, University of Yaounde I, Cameroon and General Hospital Douala, Cameroon

Oudou Njoya

Faculty of Medicine and Biomedical Sciences, University of Yaounde I, Cameroon

Wilfred Fon Mbacham

Faculty of Medicine and Biomedical Sciences, University of Yaounde I, Cameroon and Biotechnology Centre, University of Yaounde I, Cameroon

Nathan Wolfe

Global Virus Cameroon, Yaounde, Cameroon

Stuart Ray

Hepatitis Center, Johns Hopkins School of Medicine, Johns Hopkins University, USA

*Author to whom correspondence should be addressed.


Abstract

HCV infection is endemic in Cameroon. A Direct acting agent (DAAs), sofosbuvir that target the HCV non-structural 5B RNA-dependent RNA polymerase (NS5B RdRp) has recently been incorporated into the standard of care in Cameroon but no drug resistance study to this DAA has been reported in Cameroon. From the laboratory, 157 sequences were obtained and 252 downloaded from the Los Alamos HCV Sequence Database, of which 45 were Core (C), 112 were envelope (E1) and 252 were NS5B sequences were characterized by phylogeny. Drug resistance pattern in the NS5B gene was analyzed using the Geno2Pheno HCV 0.92 tool. Genotypes 1, 2 and 4 were identified. Several drug resistance-associated mutations in the NS5B gene that confer susceptibility (S282T (0.4%), and M414T (0.4%), I434M (2.8%), M414L (6.0%), C289L (13.5%) that confer possible resistance as well as (F415Y (41.3%) and V179A (4.0%) of unknown effect on sofosbuvir (SOF) were identified. There is a low level resistance rate to SOF in Cameroon.

Keywords: Genotypes, NS5B inhibitors, resistance, sofosbuvir, direct-acting agent


How to Cite

Torimiro, Judith Ndongo, Laure Arlette Tchapda, Maurice Boda, Jude Saber Bimela, Dale Netski, Désire Takou, Donald Scot Burke, et al. 2016. “Hepatitis C Virus Genetic Diversity and Drug Mutational Analysis in Cameroon: 1992 to 2013”. Microbiology Research Journal International 17 (1):1-10. https://doi.org/10.9734/BMRJ/2016/28823.

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