Near full genome characterization of HIV-1 unique recombinant forms in Cameroon reveals dominant CRF02_AG and F2 recombination patterns.


Journal

Journal of the International AIDS Society
ISSN: 1758-2652
Titre abrégé: J Int AIDS Soc
Pays: Switzerland
ID NLM: 101478566

Informations de publication

Date de publication:
07 2019
Historique:
received: 19 12 2018
accepted: 04 07 2019
entrez: 30 7 2019
pubmed: 30 7 2019
medline: 28 4 2020
Statut: ppublish

Résumé

In Cameroon, a manifold diversity of HIV strains exists with CRF02_AG and unique recombinant forms (URFs) being the predominant strains. In recent years, a steady increase in URFs and clade F2 viruses has been monitored through partial genome sequencing. There is an information gap in the characterization of emerging URFs along the full genome, which is needed to address the challenges URFs pose towards diagnosis, treatment and HIV-1 vaccine design. Eighteen Cameroonian URFs from samples collected between the years 2000 and 2015 were studied using a newly developed near full genome sequencing (NFGS) protocol based on variable nested RT-PCRs with a versatile primer set. Near full genomes were characterized for recombination patterns and sequence signatures with possible impact on antiretroviral treatment or Env-directed immune responses. Third-generation sequencing (3GS) of near full or half genomes (HGs) gave insight into intra-patient URF diversity. The characterized URFs were composed of a broad variety of subtypes and recombinants including A, F, G, CRF01_AE, CRF02_AG and CRF22_01A1. Phylogenetic analysis unveiled dominant CRF02_AG and F2 recombination patterns. 3GS indicated a high intra-patient URF diversity with up to four distinct viral sub-populations present in plasma at the same time. URF pol genomic analysis revealed a number of accessory drug resistance mutations (DRMs) in the ART-naïve participants. Genotypic env analysis suggests CCR5 usage in 14/18 samples and identified deviations at residues, critical for gp120/gp41 interphase and CD4 binding site broadly neutralizing antibodies in more than half of the studied URFs. V1V2 sites of immune pressure in the human RV144 vaccine study varied in more than a third of URFs. This study identified novel mosaic patterns in URFs in Cameroon. In line with the regional predominance of CRF_02AG and the increased prevalence of clade F2, prominent CRF_02AG and F2 background patterns were observed underlying the URFs. In the context of the novel mosaic genomes, the impact of the identified accessory DRMs and Env epitope variations on treatment and immune control remains elusive. The evolving diversity of HIV-1 URFs in Cameroon requires continuous monitoring to respond to the increasing challenges for diagnosis, antiretroviral treatment and prevention.

Identifiants

pubmed: 31353798
doi: 10.1002/jia2.25362
pmc: PMC6661401
doi:

Substances chimiques

Anti-HIV Agents 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e25362

Subventions

Organisme : Welcome Trust
ID : 107
Pays : International
Organisme : Welcome Trust
ID : 752/Z/15/Z
Pays : International

Informations de copyright

© 2019 The Authors. Journal of the International AIDS Society published by John Wiley & Sons Ltd on behalf of the International AIDS Society.

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Auteurs

Andrew N Banin (AN)

Department of Pathology, New York University School of Medicine, New York, NY, USA.
Faculty of Medicine and Biomedical Sciences, University of Yaoundé 1, Yaoundé, Cameroon.

Michael Tuen (M)

Department of Pathology, New York University School of Medicine, New York, NY, USA.

Jude S Bimela (JS)

Department of Pathology, New York University School of Medicine, New York, NY, USA.
Faculty of Science, Department of Biochemistry, University of Yaoundé 1, Yaoundé, Cameroon.

Marcel Tongo (M)

Center of Research for Emerging and Re-Emerging Diseases (CREMER), Institute of Medical Research and Study of Medicinal Plants, Yaoundé, Cameroon.

Paul Zappile (P)

Department of Pathology, New York University School of Medicine, New York, NY, USA.

Alireza Khodadadi-Jamayran (A)

Applied Bioinformatics Laboratories (ABL) and Genome Technology Center (GTC), Division of Advanced Research Technologies (DART), New York University Langone Medical Center, New York, NY, USA.

Aubin J Nanfack (AJ)

Department of Pathology, New York University School of Medicine, New York, NY, USA.
Medical Diagnostic Center, Yaoundé, Cameroon.
Chantal Biya International Reference Center for Research on HIV/AIDS Prevention and Management, Yaoundé, Cameroon.

Iheanyi O Okonko (IO)

Virus Research Unit, Department of Microbiology, University of Port Harcourt, Port Harcourt, Nigeria.

Josephine Meli (J)

Medical Diagnostic Center, Yaoundé, Cameroon.

Xiaohong Wang (X)

Manhattan Veterans Affairs Harbor Healthcare Systems, New York, NY, USA.

Dora Mbanya (D)

Faculty of Medicine and Biomedical Sciences, University of Yaoundé 1, Yaoundé, Cameroon.

Jeanne Ngogang (J)

Faculty of Medicine and Biomedical Sciences, University of Yaoundé 1, Yaoundé, Cameroon.

Miroslaw K Gorny (MK)

Department of Pathology, New York University School of Medicine, New York, NY, USA.

Adriana Heguy (A)

Department of Pathology, New York University School of Medicine, New York, NY, USA.

Charles Fokunang (C)

Faculty of Medicine and Biomedical Sciences, University of Yaoundé 1, Yaoundé, Cameroon.

Ralf Duerr (R)

Department of Pathology, New York University School of Medicine, New York, NY, USA.
Manhattan Veterans Affairs Harbor Healthcare Systems, New York, NY, USA.

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