Publication:
HIV-1 Genetic Diversity, Volume II

dc.contributor.authorTee, Kok Keng
dc.contributor.authorThomson, Michael M
dc.contributor.authorHemelaar, Joris
dc.date.accessioned2025-01-24T09:49:09Z
dc.date.available2025-01-24T09:49:09Z
dc.date.issued2022
dc.description.abstractHIV-1 acquires mutations over time and the virus can also recombine when undergoing replication. Recombination between different HIV-1 subtypes can produce mosaic viral strains which, when causing epidemic spread, are called circulating recombining forms (CRFs). Mutation and recombination lead to genetic diversification onto which evolutionary selection pressures are exerted by effects on the viral replication, transmission, pathogenesis and the immune response. As a result, HIV-1 subtypes have diversified over time and 90 distinct CRFs have been identified globally so far. Phylodynamic and phylogeographic studies estimating the spatiotemporal origin of HIV-1 variants at population level establishes the role of transmission networks in contributing to the rise in new HIV-1 infections. These networks, if left uninterrupted by means of effective intervention strategies, will most likely continue to grow and result in sustained transmission. Understanding the dynamics of growth and dispersal of HIV-1 variants, as well as the cutting edge methods used in such analysis, can be useful to assess the evolution of an epidemic and the impact of public health interventions. However, the epidemiological and molecular mechanisms which contribute to the emergence of recombinants are incompletely understood. Moreover, a better understanding of the effects of HIV-1 genetic diversity on clinical characteristics such as transmission, pathogenesis and disease progression as well as implication for management such as diagnosis, viral load measurement and treatment, are essential for the containment of the HIV epidemic. Finally, the enormous diversity of the HIV-1 pandemic poses a major challenge to the development of a globally effective HIV vaccine.
dc.description.peerreviewed
dc.identifier.citationTee, K. K., Thomson, M. M., Hemelaar, J., eds. (2022). HIV-1 Genetic Diversity, Volume II. Lausanne: Frontiers Media SA. doi: 10.3389/978-2-88976-940-7
dc.identifier.doi10.3389/978-2-88976-940-7
dc.identifier.isbn9782889769407
dc.identifier.issn1664-8714
dc.identifier.urihttps://hdl.handle.net/20.500.12105/26122
dc.language.isoeng
dc.publisherFrontiers Media
dc.relation.ispartofseriesResearch Topics
dc.relation.publisherversionhttps://doi.org/10.3389/978-2-88976-940-7
dc.repisalud.centroISCIII::Centro Nacional de Microbiología (CNM)
dc.repisalud.institucionISCIII
dc.rights.accessRightsopen access
dc.rights.licenseAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectHuman Immunodeficiency Virus
dc.subjectGenetic Diversity
dc.subjectMolecular Epidemiology
dc.subjectRecombination
dc.subjectSubtype
dc.titleHIV-1 Genetic Diversity, Volume II
dc.typebook
dc.type.hasVersionVoR
dspace.entity.typePublication
relation.isAuthorOfPublicationad673934-9665-4352-b498-c694bf04ae3c
relation.isAuthorOfPublication.latestForDiscoveryad673934-9665-4352-b498-c694bf04ae3c
relation.isPublisherOfPublication9f9fa5ea-093b-43d8-bf2c-5bd65d08a802
relation.isPublisherOfPublication.latestForDiscovery9f9fa5ea-093b-43d8-bf2c-5bd65d08a802

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