Evidence map›Paper›PMID 40741381›Full record

ArticleJAC-antimicrobial resistance2025

Highly genetically diverse variants of hepatitis C virus still predominate in Cameroon but with low frequency of mutations associated to resistance of NS5B polymerase-targeted antivirals.

Fabrice Levoa Eteme, Nadege Mafopa Goumkwa, Alliance-Laure Otam, Cindy Lobe, Clauvis Kunkeng Yengo, Mathurin Kowo, Laure Tchapda, Inoussa Pempeme, Williams Anderson Ngameleu, Junior Ekunidi Engarimbi and 9 more

Abstract read
In one paragraph

Article in JAC-antimicrobial resistance, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors.

Fabrice Levoa EtemeMolecular Biology Laboratory, Chantal Biya International Reference Centre for Research on Prevention and Management of HIV/AIDS (CIRCB), Yaoundé, Cameroon.
Nadege Mafopa GoumkwaMolecular Biology Laboratory, Chantal Biya International Reference Centre for Research on Prevention and Management of HIV/AIDS (CIRCB), Yaoundé, Cameroon.
Alliance-Laure OtamMolecular Biology Laboratory, Chantal Biya International Reference Centre for Research on Prevention and Management of HIV/AIDS (CIRCB), Yaoundé, Cameroon.
Cindy LobeMolecular Biology Laboratory, Chantal Biya International Reference Centre for Research on Prevention and Management of HIV/AIDS (CIRCB), Yaoundé, Cameroon.
Clauvis Kunkeng YengoDepartment of Biochemistry, Faculty of Sciences, University of Yaoundé I, Yaoundé, Cameroon.
Mathurin KowoDepartment of Internal Medicine, Faculty of Medicine and Biomedical Sciences, University of Yaoundé I, Yaoundé, Cameroon.
Laure TchapdaDepartment of Biomedical Sciences, Faculty of Science, University of Ngaoundéré, Ngaoundéré, Cameroon.
Inoussa PempemeDepartment of Clinical Biology, Faculty of Medicine and Pharmaceutical Sciences, University of Douala, Douala, Cameroon.
Williams Anderson NgameleuDepartment of Biochemistry and Molecular Biology, Faculty of Sciences, University of Buea, Buea, Cameroon.
Junior Ekunidi EngarimbiDepartment of Biochemistry and Molecular Biology, Faculty of Sciences, University of Buea, Buea, Cameroon.
Signang Alberic NdonkuDepartment of Biochemistry, Faculty of Medicine and Biomedical Sciences, University of Yaoundé I, Yaoundé, Cameroon.
Diapa Nana YannickDepartment of Biochemistry and Molecular Biology, Faculty of Sciences, University of Buea, Buea, Cameroon.
Patrick Lebon AwoumouDepartment of Biochemistry, Faculty of Medicine and Biomedical Sciences, University of Yaoundé I, Yaoundé, Cameroon.
Marie-Ange KwizeraDepartment of Microbiology, Haematology, Parasitology, and Infectious Diseases, Faculty of Medicine and Biomedical Sciences, University of Yaoundé I, Yaoundé, Cameroon.
Njoya OudouDepartment of Internal Medicine, Faculty of Medicine and Biomedical Sciences, University of Yaoundé I, Yaoundé, Cameroon.
Marie Claire Assoumou OkomoDepartment of Microbiology, Haematology, Parasitology, and Infectious Diseases, Faculty of Medicine and Biomedical Sciences, University of Yaoundé I, Yaoundé, Cameroon.
Charles Ntungwen FokunangDepartment of Pharmacotoxicology and Pharmacokinetics, Faculty of Medicine and Biomedical Sciences, University of Yaoundé I, Yaoundé, Cameroun.
Henry Namme LumaDepartment of Internal Medicine, Douala General Hospital, Douala, Cameroon.
Judith Ndongo Embola TorimiroMolecular Biology Laboratory, Chantal Biya International Reference Centre for Research on Prevention and Management of HIV/AIDS (CIRCB), Yaoundé, Cameroon.

Funding

TUBERCULOSIS INTERNATIONAL TRAINING AND RESEARCH PROGRAMD43TW000010 · FIC · JOHNS HOPKINS UNIVERSITY · PI BEYRER, CHRISTOPHER C. · 1988 to 2012
$19.8M
Antiretroviral Activity of TRIM5alphaR01AI063987 · NIAID · DANA-FARBER CANCER INSTITUTE · PI SODROSKI, JOSEPH G · 2005 to 2014
$4.2M
Structure of the Retroviral Restriction Factor, TRIM5alphaR21AI076094 · NIAID · DANA-FARBER CANCER INST · PI SODROSKI, JOSEPH G · 2007 to 2008
$463k
FIC NIH HHS D43 TW000010NIAID NIH HHS R01 AI063987NIAID NIH HHS R21 AI076094
6 · The paper itself

Abstract

Background: 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. Methods: 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). Results: 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%. Conclusion: 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.

Identifiers

PMID40741381
PMCPMC12308484

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.