The genealogical population dynamics of HIV-1 in a large transmission chain: bridging within and among host evolutionary rates.

Transmission lies at the interface of human immunodeficiency virus type 1 (HIV-1) evolution within and among hosts and separates distinct selective pressures that impose differences in both the mode of diversification and the tempo of evolution. In the absence of comprehensive direct comparative ana...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Bram Vrancken, Andrew Rambaut, Marc A Suchard, Alexei Drummond, Guy Baele, Inge Derdelinckx, Eric Van Wijngaerden, Anne-Mieke Vandamme, Kristel Van Laethem, Philippe Lemey
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2014
Materias:
Acceso en línea:https://doaj.org/article/a03e48b5162d400ab068fc46bad73c55
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:a03e48b5162d400ab068fc46bad73c55
record_format dspace
spelling oai:doaj.org-article:a03e48b5162d400ab068fc46bad73c552021-11-18T05:53:01ZThe genealogical population dynamics of HIV-1 in a large transmission chain: bridging within and among host evolutionary rates.1553-734X1553-735810.1371/journal.pcbi.1003505https://doaj.org/article/a03e48b5162d400ab068fc46bad73c552014-04-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24699231/pdf/?tool=EBIhttps://doaj.org/toc/1553-734Xhttps://doaj.org/toc/1553-7358Transmission lies at the interface of human immunodeficiency virus type 1 (HIV-1) evolution within and among hosts and separates distinct selective pressures that impose differences in both the mode of diversification and the tempo of evolution. In the absence of comprehensive direct comparative analyses of the evolutionary processes at different biological scales, our understanding of how fast within-host HIV-1 evolutionary rates translate to lower rates at the between host level remains incomplete. Here, we address this by analyzing pol and env data from a large HIV-1 subtype C transmission chain for which both the timing and the direction is known for most transmission events. To this purpose, we develop a new transmission model in a Bayesian genealogical inference framework and demonstrate how to constrain the viral evolutionary history to be compatible with the transmission history while simultaneously inferring the within-host evolutionary and population dynamics. We show that accommodating a transmission bottleneck affords the best fit our data, but the sparse within-host HIV-1 sampling prevents accurate quantification of the concomitant loss in genetic diversity. We draw inference under the transmission model to estimate HIV-1 evolutionary rates among epidemiologically-related patients and demonstrate that they lie in between fast intra-host rates and lower rates among epidemiologically unrelated individuals infected with HIV subtype C. Using a new molecular clock approach, we quantify and find support for a lower evolutionary rate along branches that accommodate a transmission event or branches that represent the entire backbone of transmitted lineages in our transmission history. Finally, we recover the rate differences at the different biological scales for both synonymous and non-synonymous substitution rates, which is only compatible with the 'store and retrieve' hypothesis positing that viruses stored early in latently infected cells preferentially transmit or establish new infections upon reactivation.Bram VranckenAndrew RambautMarc A SuchardAlexei DrummondGuy BaeleInge DerdelinckxEric Van WijngaerdenAnne-Mieke VandammeKristel Van LaethemPhilippe LemeyPublic Library of Science (PLoS)articleBiology (General)QH301-705.5ENPLoS Computational Biology, Vol 10, Iss 4, p e1003505 (2014)
institution DOAJ
collection DOAJ
language EN
topic Biology (General)
QH301-705.5
spellingShingle Biology (General)
QH301-705.5
Bram Vrancken
Andrew Rambaut
Marc A Suchard
Alexei Drummond
Guy Baele
Inge Derdelinckx
Eric Van Wijngaerden
Anne-Mieke Vandamme
Kristel Van Laethem
Philippe Lemey
The genealogical population dynamics of HIV-1 in a large transmission chain: bridging within and among host evolutionary rates.
description Transmission lies at the interface of human immunodeficiency virus type 1 (HIV-1) evolution within and among hosts and separates distinct selective pressures that impose differences in both the mode of diversification and the tempo of evolution. In the absence of comprehensive direct comparative analyses of the evolutionary processes at different biological scales, our understanding of how fast within-host HIV-1 evolutionary rates translate to lower rates at the between host level remains incomplete. Here, we address this by analyzing pol and env data from a large HIV-1 subtype C transmission chain for which both the timing and the direction is known for most transmission events. To this purpose, we develop a new transmission model in a Bayesian genealogical inference framework and demonstrate how to constrain the viral evolutionary history to be compatible with the transmission history while simultaneously inferring the within-host evolutionary and population dynamics. We show that accommodating a transmission bottleneck affords the best fit our data, but the sparse within-host HIV-1 sampling prevents accurate quantification of the concomitant loss in genetic diversity. We draw inference under the transmission model to estimate HIV-1 evolutionary rates among epidemiologically-related patients and demonstrate that they lie in between fast intra-host rates and lower rates among epidemiologically unrelated individuals infected with HIV subtype C. Using a new molecular clock approach, we quantify and find support for a lower evolutionary rate along branches that accommodate a transmission event or branches that represent the entire backbone of transmitted lineages in our transmission history. Finally, we recover the rate differences at the different biological scales for both synonymous and non-synonymous substitution rates, which is only compatible with the 'store and retrieve' hypothesis positing that viruses stored early in latently infected cells preferentially transmit or establish new infections upon reactivation.
format article
author Bram Vrancken
Andrew Rambaut
Marc A Suchard
Alexei Drummond
Guy Baele
Inge Derdelinckx
Eric Van Wijngaerden
Anne-Mieke Vandamme
Kristel Van Laethem
Philippe Lemey
author_facet Bram Vrancken
Andrew Rambaut
Marc A Suchard
Alexei Drummond
Guy Baele
Inge Derdelinckx
Eric Van Wijngaerden
Anne-Mieke Vandamme
Kristel Van Laethem
Philippe Lemey
author_sort Bram Vrancken
title The genealogical population dynamics of HIV-1 in a large transmission chain: bridging within and among host evolutionary rates.
title_short The genealogical population dynamics of HIV-1 in a large transmission chain: bridging within and among host evolutionary rates.
title_full The genealogical population dynamics of HIV-1 in a large transmission chain: bridging within and among host evolutionary rates.
title_fullStr The genealogical population dynamics of HIV-1 in a large transmission chain: bridging within and among host evolutionary rates.
title_full_unstemmed The genealogical population dynamics of HIV-1 in a large transmission chain: bridging within and among host evolutionary rates.
title_sort genealogical population dynamics of hiv-1 in a large transmission chain: bridging within and among host evolutionary rates.
publisher Public Library of Science (PLoS)
publishDate 2014
url https://doaj.org/article/a03e48b5162d400ab068fc46bad73c55
work_keys_str_mv AT bramvrancken thegenealogicalpopulationdynamicsofhiv1inalargetransmissionchainbridgingwithinandamonghostevolutionaryrates
AT andrewrambaut thegenealogicalpopulationdynamicsofhiv1inalargetransmissionchainbridgingwithinandamonghostevolutionaryrates
AT marcasuchard thegenealogicalpopulationdynamicsofhiv1inalargetransmissionchainbridgingwithinandamonghostevolutionaryrates
AT alexeidrummond thegenealogicalpopulationdynamicsofhiv1inalargetransmissionchainbridgingwithinandamonghostevolutionaryrates
AT guybaele thegenealogicalpopulationdynamicsofhiv1inalargetransmissionchainbridgingwithinandamonghostevolutionaryrates
AT ingederdelinckx thegenealogicalpopulationdynamicsofhiv1inalargetransmissionchainbridgingwithinandamonghostevolutionaryrates
AT ericvanwijngaerden thegenealogicalpopulationdynamicsofhiv1inalargetransmissionchainbridgingwithinandamonghostevolutionaryrates
AT annemiekevandamme thegenealogicalpopulationdynamicsofhiv1inalargetransmissionchainbridgingwithinandamonghostevolutionaryrates
AT kristelvanlaethem thegenealogicalpopulationdynamicsofhiv1inalargetransmissionchainbridgingwithinandamonghostevolutionaryrates
AT philippelemey thegenealogicalpopulationdynamicsofhiv1inalargetransmissionchainbridgingwithinandamonghostevolutionaryrates
AT bramvrancken genealogicalpopulationdynamicsofhiv1inalargetransmissionchainbridgingwithinandamonghostevolutionaryrates
AT andrewrambaut genealogicalpopulationdynamicsofhiv1inalargetransmissionchainbridgingwithinandamonghostevolutionaryrates
AT marcasuchard genealogicalpopulationdynamicsofhiv1inalargetransmissionchainbridgingwithinandamonghostevolutionaryrates
AT alexeidrummond genealogicalpopulationdynamicsofhiv1inalargetransmissionchainbridgingwithinandamonghostevolutionaryrates
AT guybaele genealogicalpopulationdynamicsofhiv1inalargetransmissionchainbridgingwithinandamonghostevolutionaryrates
AT ingederdelinckx genealogicalpopulationdynamicsofhiv1inalargetransmissionchainbridgingwithinandamonghostevolutionaryrates
AT ericvanwijngaerden genealogicalpopulationdynamicsofhiv1inalargetransmissionchainbridgingwithinandamonghostevolutionaryrates
AT annemiekevandamme genealogicalpopulationdynamicsofhiv1inalargetransmissionchainbridgingwithinandamonghostevolutionaryrates
AT kristelvanlaethem genealogicalpopulationdynamicsofhiv1inalargetransmissionchainbridgingwithinandamonghostevolutionaryrates
AT philippelemey genealogicalpopulationdynamicsofhiv1inalargetransmissionchainbridgingwithinandamonghostevolutionaryrates
_version_ 1718424684608880640