Author/Authors :
Blackard Jason T. نويسنده Division of Digestive Disease, Department of Internal Medicine, University of Cincinnati College of Medicine, Cincinnati, OH, USA , Petronella Gededzha Maemu نويسنده HIV and Hepatitis Research Unit, Department of Virology,
Sefako Makgatho Health Sciences University/National Health
Laboratory Service, Pretoria, South Africa , Mphahlele M. Jeffrey نويسنده HIV and Hepatitis Research Unit, Department of Virology,
Sefako Makgatho Health Sciences University/National Health
Laboratory Service, Pretoria, South Africa , Gloria Selabe Selokela نويسنده HIV and Hepatitis Research Unit, Department of Virology,
Sefako Makgatho Health Sciences University/National Health
Laboratory Service, Pretoria, South Africa
Abstract :
Background HCV NS5B is a major target for drugs that directly
inhibit viral replication. Naturally occurring mutations that reduce
susceptibility to NS5B inhibitors have been reported. Objectives The
present study aimed at screening treatment resistance mutations in the
NS5B region in South Africa. Methods The study comprised 42 NS5B
sequences (amino acids 228 - 335), derived from treatment-naïve
HCV-infected patients at Dr George Mukhari Academic hospital. Nucleotide
sequences were aligned, translated into amino acids, and compared to
mutations associated with drug resistance described in the literature.
Results The most common mutation in this study was Q309R, which was
present in all genotypes except genotype 1b. Mutation A333E was detected
only in genotype 5a. The NS5B polymorphism C316N, which is associated
with resistance to HCV-796, was found in 3 of 4 genotype 1b sequences.
The resistance mutations D244N, S282T, C316Y, S326G, and T329I were not
detected in any of the analyzed sequences. Position 309 was under
positive selection in genotype 5a. Conclusions The data indicated the
presence of previously described NS5B resistance mutations in South
African treatment-naïve patients, suggesting that drug resistance
testing would be useful prior to the initiation of antiviral therapy for
HCV.