Levoa Eteme Fabrice, Mafopa Goumkwa Nadege, Otam Alliance-Laure, Lobe Cindy, Yengo Clauvis Kunkeng, Kowo Mathurin, Tchapda Laure, Pempeme Inoussa, Ngameleu Williams Anderson, Engarimbi Junior Ekunidi, Ndonku Signang Alberic, Yannick Diapa Nana, Awoumou Patrick Lebon, Kwizera Marie-Ange, Oudou Njoya, Okomo Marie Claire Assoumou, Fokunang Charles Ntungwen, Luma Henry Namme, Torimiro Judith Ndongo Embola
Molecular Biology Laboratory, Chantal Biya International Reference Centre for Research on Prevention and Management of HIV/AIDS (CIRCB), Yaoundé, Cameroon.
Department of Microbiology, Haematology, Parasitology, and Infectious Diseases, Faculty of Medicine and Biomedical Sciences, University of Yaoundé I, Yaoundé, Cameroon.
JAC Antimicrob Resist. 2025 Jul 30;7(4):dlaf114. doi: 10.1093/jacamr/dlaf114. eCollection 2025 Aug.
Hepatitis C is of low endemicity (<2%) in the general population in Cameroon, with genotypes (GTs) 1, 2 and 4 reported frequently identified. In 2016, direct-acting antiviral agents (DAAs) were included in the Treatment Guidelines for hepatitis C in Cameroon. The aim of this study was to investigate hepatitis C virus (HCV) variability and frequency of NS5B naturally occurring polymorphisms and transmitted resistance-associated mutations or substitutions (RAMs or RASs) in DAAs-naïve patients.
From 240 HCV-infected, DAA-naïve individuals, the NS5B region of 92 samples were sequenced, genotyped by phylogeny using MEGA 11.0.13 software and analysed for polymorphisms conferring resistance to polymerase inhibitors using bioinformatics tools (Geno2Pheno HCV 0.92 and BioEdit version 7.2.5).
Thirty-two GT1 (34.8%), 37 GT2 (40.2%), 22 GT4 (23.9%) and 1 GT5 (1.1%), 13 subtypes (1e, 1g, 1h, 1j, 1l, 2j, 2r, 4a, 4f, 4l, 4p, 4t and 5a) were found. Thirty-four GT2 sequences clustered together without any reference sequences and therefore could not be subtyped. The NS5B S282T resistance-associated substitutions was not detected in any sample. However, the polymorphisms of unreported resistance-associated impact in positions 316 and 321 were identified: C316H (8.7%), C316N (18.5%), V321I (6.5%) and a double mutant C316H/V321I (4.3%). Comparison of GTs obtained by a commercial PCR kit versus Sanger sequencing and phylogeny of the NS5B region, showed a discrepancy of 30%.
Genotype 5 was identified for the first time in Cameroon. The frequency of V321I and C316H/N polymorphism with unknown impact on NS5B polymerase inhibitors is increasing in Cameroon.
在喀麦隆普通人群中,丙型肝炎流行率较低(<2%),常见的基因型(GTs)为1、2和4型。2016年,直接抗病毒药物(DAAs)被纳入喀麦隆丙型肝炎治疗指南。本研究旨在调查初治患者中丙型肝炎病毒(HCV)的变异性、NS5B自然发生的多态性频率以及与传播相关的耐药突变或替代(RAMs或RASs)。
从240例感染HCV且未使用过DAA的个体中,对92份样本的NS5B区域进行测序,使用MEGA 11.0.13软件通过系统发育进行基因分型,并使用生物信息学工具(Geno2Pheno HCV 0.92和BioEdit 7.2.5版本)分析对聚合酶抑制剂具有抗性的多态性。
发现32例GT1型(34.8%)、37例GT2型(40.2%)、22例GT4型(23.9%)、1例GT5型(1.1%)以及13个亚型(1e、1g、1h、1j、1l、2j、2r、4a、4f、4l、4p、4t和5a)。34个GT2序列聚集在一起,没有任何参考序列,因此无法进一步分型。在任何样本中均未检测到NS5B S282T耐药相关替代。然而,在316和321位发现了未报道的具有耐药相关影响的多态性:C316H(8.7%)、C316N(18.5%)、V321I(6.5%)以及双突变体C316H/V321I(4.3%)。通过商业PCR试剂盒获得的GTs与Sanger测序以及NS5B区域的系统发育比较显示,差异为30%。
在喀麦隆首次鉴定出5型基因型。在喀麦隆,对NS5B聚合酶抑制剂影响未知的V321I和C316H/N多态性频率正在增加。