TY - JOUR
T1 - Prevalence of Ns5B resistance mutations in hepatitis C virus (HCV) treatment naive South Africans
AU - Gededzha, Maemu Petronella
AU - Mphahlele, M. Jeffrey
AU - Blackard, Jason T.
AU - Selabe, Selokelagloria
N1 - Publisher Copyright:
© 2017, Hepatitis Monthly.
PY - 2017/6
Y1 - 2017/6
N2 - 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.
AB - 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.
KW - HCV
KW - Hepatitis C Virus
KW - NS5B
KW - Resistance mutations
KW - South Africa
UR - http://www.scopus.com/inward/record.url?scp=85027033876&partnerID=8YFLogxK
U2 - 10.5812/hepatmon.14248
DO - 10.5812/hepatmon.14248
M3 - Article
AN - SCOPUS:85027033876
SN - 1735-143X
VL - 17
JO - Hepatitis Monthly
JF - Hepatitis Monthly
IS - 6
M1 - e14248
ER -