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Evolutionary dynamics of HIV at multiple spatial and temporal scales

Infectious diseases remain a formidable challenge to human health, and understanding pathogen evolution is crucial to designing effective therapeutics and control strategies. Here, we review important evolutionary aspects of HIV infection, highlighting the concept of selection at multiple spatial an...

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Autores principales: Hill, Alison L., Rosenbloom, Daniel I. S., Nowak, Martin A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7080006/
https://www.ncbi.nlm.nih.gov/pubmed/22552382
http://dx.doi.org/10.1007/s00109-012-0892-1
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author Hill, Alison L.
Rosenbloom, Daniel I. S.
Nowak, Martin A.
author_facet Hill, Alison L.
Rosenbloom, Daniel I. S.
Nowak, Martin A.
author_sort Hill, Alison L.
collection PubMed
description Infectious diseases remain a formidable challenge to human health, and understanding pathogen evolution is crucial to designing effective therapeutics and control strategies. Here, we review important evolutionary aspects of HIV infection, highlighting the concept of selection at multiple spatial and temporal scales. At the smallest scale, a single cell may be infected by multiple virions competing for intracellular resources. Recombination and phenotypic mixing introduce novel evolutionary dynamics. As the virus spreads between cells in an infected individual, it continually evolves to circumvent the immune system. We discuss evolutionary mechanisms of HIV pathogenesis and progression to AIDS. Viral spread throughout the human population can lead to changes in virulence and the transmission of immune-evading variation. HIV emerged as a human pathogen due to selection occurring between different species, adapting from related viruses of primates. HIV also evolves resistance to antiretroviral drugs within a single infected host, and we explore the possibility for the spread of these strains between hosts, leading to a drug-resistant epidemic. We investigate the role of latency, drug-protected compartments, and direct cell-to-cell transmission on viral evolution. The introduction of an HIV vaccine may select for viral variants that escape vaccine control, both within an individual and throughout the population. Due to the strong selective pressure exerted by HIV-induced morbidity and mortality in many parts of the world, the human population itself may be co-evolving in response to the HIV pandemic. Throughout the paper, we focus on trade-offs between costs and benefits that constrain viral evolution and accentuate how selection pressures differ at different levels of selection. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00109-012-0892-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-70800062020-03-23 Evolutionary dynamics of HIV at multiple spatial and temporal scales Hill, Alison L. Rosenbloom, Daniel I. S. Nowak, Martin A. J Mol Med (Berl) Review Infectious diseases remain a formidable challenge to human health, and understanding pathogen evolution is crucial to designing effective therapeutics and control strategies. Here, we review important evolutionary aspects of HIV infection, highlighting the concept of selection at multiple spatial and temporal scales. At the smallest scale, a single cell may be infected by multiple virions competing for intracellular resources. Recombination and phenotypic mixing introduce novel evolutionary dynamics. As the virus spreads between cells in an infected individual, it continually evolves to circumvent the immune system. We discuss evolutionary mechanisms of HIV pathogenesis and progression to AIDS. Viral spread throughout the human population can lead to changes in virulence and the transmission of immune-evading variation. HIV emerged as a human pathogen due to selection occurring between different species, adapting from related viruses of primates. HIV also evolves resistance to antiretroviral drugs within a single infected host, and we explore the possibility for the spread of these strains between hosts, leading to a drug-resistant epidemic. We investigate the role of latency, drug-protected compartments, and direct cell-to-cell transmission on viral evolution. The introduction of an HIV vaccine may select for viral variants that escape vaccine control, both within an individual and throughout the population. Due to the strong selective pressure exerted by HIV-induced morbidity and mortality in many parts of the world, the human population itself may be co-evolving in response to the HIV pandemic. Throughout the paper, we focus on trade-offs between costs and benefits that constrain viral evolution and accentuate how selection pressures differ at different levels of selection. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00109-012-0892-1) contains supplementary material, which is available to authorized users. Springer-Verlag 2012-05-03 2012 /pmc/articles/PMC7080006/ /pubmed/22552382 http://dx.doi.org/10.1007/s00109-012-0892-1 Text en © Springer-Verlag 2012 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Review
Hill, Alison L.
Rosenbloom, Daniel I. S.
Nowak, Martin A.
Evolutionary dynamics of HIV at multiple spatial and temporal scales
title Evolutionary dynamics of HIV at multiple spatial and temporal scales
title_full Evolutionary dynamics of HIV at multiple spatial and temporal scales
title_fullStr Evolutionary dynamics of HIV at multiple spatial and temporal scales
title_full_unstemmed Evolutionary dynamics of HIV at multiple spatial and temporal scales
title_short Evolutionary dynamics of HIV at multiple spatial and temporal scales
title_sort evolutionary dynamics of hiv at multiple spatial and temporal scales
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7080006/
https://www.ncbi.nlm.nih.gov/pubmed/22552382
http://dx.doi.org/10.1007/s00109-012-0892-1
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