Dissecting HIV Virulence: Heritability of Setpoint Viral Load, CD4+ T-Cell Decline, and Per-Parasite Pathogenicity

Autor: Enos Bernasconi, Venelin Mitov, Huldrych F. Günthard, Manuel Battegay, Jacques Fellay, Matthias Cavassini, Gabriel E. Leventhal, Roland R. Regoes, Sabine Yerly, Sebastian Bonhoeffer, Jürg Böni, Viktor Müller, Vincent Aubert, Patrick Schmid, Andri Rauch, Alexandra Calmy, Thomas Klimkait, Roger D. Kouyos, Alexandra U. Scherrer, Frederic Bertels, Alex Marzel
Přispěvatelé: Swiss HIV Cohort Study
Rok vydání: 2017
Předmět:
CD4-Positive T-Lymphocytes
Male
0301 basic medicine
HIV Infections
heritability
Cohort Studies
Genotype
Stabilizing selection
Pathogen
disease tolerance
Phylogeny
ddc:616
Genetics
0303 health sciences
Virulence
Phylogenetic tree
Viral Load
3. Good health
Phenotype
medicine.anatomical_structure
Female
Viral load
evolution of virulence
Adult
T cell
030106 microbiology
610 Medicine & health
Biology
Virus
03 medical and health sciences
per-parasite pathogenicity
HIV
Phylogenetics
medicine
Humans
Molecular Biology
Discoveries
Ecology
Evolution
Behavior and Systematics

030304 developmental biology
030306 microbiology
Directional selection
Heritability
Virology
CD4 Lymphocyte Count
030104 developmental biology
CD4 Lymphocyte Count/methods
CD4-Positive T-Lymphocytes/pathology
HIV Infections/transmission
HIV-1/genetics
Viral Load/methods
HIV-1
Zdroj: Bertels, Frederic; Marzel, Alex; Leventhal, Gabriel; Mitov, Venelin; Fellay, Jacques; Günthard, Huldrych F; Böni, Jürg; Yerly, Sabine; Klimkait, Thomas; Aubert, Vincent; Battegay, Manuel; Rauch, Andri; Cavassini, Matthias; Calmy, Alexandra; Bernasconi, Enos; Schmid, Patrick; Scherrer, Alexandra U; Müller, Viktor; Bonhoeffer, Sebastian; Kouyos, Roger; ... (2018). Dissecting HIV Virulence: Heritability of Setpoint Viral Load, CD4+ T Cell Decline and Per-Parasite Pathogenicity. Molecular Biology and Evolution, 35(1), pp. 27-37. Oxford University Press 10.1093/molbev/msx246
Molecular Biology and Evolution, Vol. 35, No 1 (2018) pp. 27-37
Molecular Biology and Evolution, 35 (1)
Molecular Biology and Evolution
Molecular biology and evolution, vol. 35, no. 1, pp. 27-37
ISSN: 1537-1719
0737-4038
DOI: 10.1093/molbev/msx246
Popis: Pathogen strains may differ in virulence because they attain different loads in their hosts, or because they induce different disease-causing mechanisms independent of their load. In evolutionary ecology, the latter is referred to as “per-parasite pathogenicity”. Using viral load and CD4+ T cell measures from 2014 HIV-1 subtype B infected individuals enrolled in the Swiss HIV Cohort Study, we investigated if virulence — measured as the rate of decline of CD4+ T cells — and per-parasite pathogenicity are heritable from donor to recipient. We estimated heritability by donor-recipient regressions applied to 196 previously identified transmission pairs, and by phylogenetic mixed models applied to a phylogenetic tree inferred from HIV pol sequences. Regressing the CD4+ T cell declines and per-parasite pathogenicities of the transmission pairs did not yield heritability estimates significantly different from zero. With the phylogenetic mixed model, however, our best estimate for the heritability of the CD4+ T cell decline is 17% (5%–30%), and that of the per-parasite pathogenicity is 17% (4%–29%). Further, we confirm that the set-point viral load is heritable, and estimate a heritability of 29% (12%–46%). Interestingly, the pattern of evolution of all these traits differs significantly from neutrality, and is most consistent with stabilizing selection for the set-point viral load, and with directional selection for the CD4+ T cell decline and the per-parasite pathogenicity. Our analysis shows that the viral genetype affects virulence mainly by modulating the per-parasite pathogenicity, while the indirect effect via the set-point viral load is minor.
Databáze: OpenAIRE