Phylogenetic estimation of the viral fitness landscape of HIV-1 set-point viral load

被引:0
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作者
Zhao, Lele [1 ]
Wymant, Chris [1 ]
Blanquart, Francois [2 ]
Golubchik, Tanya [1 ]
Gall, Astrid [3 ]
Bakker, Margreet [4 ]
Bezemer, Daniela [5 ]
Hall, Matthew [1 ]
Ong, Swee Hoe [6 ]
Albert, Jan [7 ,8 ]
Bannert, Norbert [9 ]
Fellay, Jacques [10 ,11 ,12 ,13 ]
Grabowski, M. Kate [14 ]
Gunsenheimer-Bartmeyer, Barbara [15 ]
Gunthard, Huldrych F. [16 ,17 ]
Kivela, Pia [18 ]
Kouyos, Roger D. [16 ,17 ]
Laeyendecker, Oliver [19 ]
Meyer, Laurence [20 ]
Porter, Kholoud [21 ]
van Sighem, Ard [5 ]
van der Valk, Marc [5 ]
Berkhout, Ben [4 ]
Kellam, Paul [22 ,23 ]
Cornelissen, Marion [4 ,24 ]
Reiss, Peter [5 ,25 ,26 ]
Fraser, Christophe [1 ]
Ferretti, Luca [1 ]
机构
[1] Univ Oxford, Li Ka Shing Ctr Hlth Informat & Discovery, Big Data Inst, Nuffield Dept Med, Old Rd Campus, Oxford OX3 7LF, England
[2] PSL Res Univ, Coll France, Ctr Interdisciplinary Res Biol CIRB, INSERM,CNRS, F-75231 Paris 05, France
[3] European Bioinformat Inst, European Mol Biol Lab, Wellcome Genome Campus, Cambridge CB10 1SD, England
[4] Univ Amsterdam, Amsterdam Univ Med Ctr, Dept Med Microbiol & Infect Prevent, Lab Expt Virol, NL-1007 MB Amsterdam, Netherlands
[5] Stichting HIV Monitoring, NL-1105 AZ Amsterdam, Netherlands
[6] Wellcome Sanger Inst, Wellcome Genome Campus, Cambridge CB10 1SA, England
[7] Karolinska Inst, Dept Microbiol Tumor & Cell Biol, S-17177 Stockholm, Sweden
[8] Karolinska Univ Hosp, Dept Clin Microbiol, S-17176 Stockholm, Sweden
[9] Robert Koch Inst, Dept Infect Dis, Div HIV & Other Retroviruses, D-13353 Berlin, Germany
[10] Ecole Polytech Fed Lausanne, Sch Life Sci, CH-1015 Lausanne, Switzerland
[11] Swiss Inst Bioinformat, CH-1015 Lausanne, Switzerland
[12] Lausanne Univ Hosp, Precis Med Unit, CH-1015 Lausanne, Switzerland
[13] Univ Lausanne, CH-1015 Lausanne, Switzerland
[14] Johns Hopkins Univ, Dept Pathol, Baltimore, MD 21287 USA
[15] Robert Koch Inst, Dept Infect Dis Epidemiol, D-13353 Berlin, Germany
[16] Univ Hosp Zurich, Div Infect Dis & Hosp Epidemiol, CH-8091 Zurich, Switzerland
[17] Univ Zurich, Inst Med Virol, CH-8057 Zurich, Switzerland
[18] Helsinki Univ Hosp, Dept Infect Dis, FI-00029 Helsinki, Finland
[19] NIAID, Div Intramural Res, NIH, Baltimore, MD 21205 USA
[20] Univ Paris Saclay, Serv Sante Publ, Hop Bicetre, APHP,INSERM CESP U1018, F-94270 Le Kremlin Bicetre, France
[21] UCL, Inst Global Hlth, London WC1N 1EH, England
[22] Kymab Ltd, Babraham Res Campus, Cambridge CB22 3AT, England
[23] Imperial Coll London, Fac Med, Dept Infect Dis, South Kensington Campus, London SW7 2AZ, England
[24] Univ Amsterdam, Dept Med Microbiol & Infect Prevent, Mol Diagnost Unit, Amsterdam Univ Med Ctr, NL-1007 MB Amsterdam, Netherlands
[25] Univ Amsterdam, Dept Global Hlth, Amsterdam Univ Med Ctr, NL-1100 DE Amsterdam, Netherlands
[26] Amsterdam Inst Global Hlth & Dev, NL-1100 DE Amsterdam, Netherlands
基金
欧洲研究理事会;
关键词
HIV-1; between-host evolution; tansmission fitness; set-point viral load; ANTIRETROVIRAL THERAPY; PROGNOSTIC MARKERS; RNA; HERITABILITY; INITIATION; DIAGNOSIS; VIRULENCE; TIME;
D O I
10.1093/ve/veac022
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Set-point viral load (SPVL), a common measure of human immunodeficiency virus (HIV)-1 virulence, is partially determined by viral genotype. Epidemiological evidence suggests that this viral property has been under stabilising selection, with a typical optimum for the virus between 10(4) and 10(5) copies of viral RNA per ml. Here we aimed to detect transmission fitness differences between viruses from individuals with different SPVLs directly from phylogenetic trees inferred from whole-genome sequences. We used the local branching index (LBI) as a proxy for transmission fitness. We found that LBI is more sensitive to differences in infectiousness than to differences in the duration of the infectious state. By analysing subtype-B samples from the Bridging the Evolution and Epidemiology of HIV in Europe project, we inferred a significant positive relationship between SPVL and LBI up to approximately 10(5) copies/ml, with some evidence for a peak around this value of SPVL. This is evidence of selection against low values of SPVL in HIV-1 subtype-B strains, likely related to lower infectiousness, and perhaps a peak in the transmission fitness in the expected range of SPVL. The less prominent signatures of selection against higher SPVL could be explained by an inherent limit of the method or the deployment of antiretroviral therapy.
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页数:8
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