A Phylogeny-aware GWAS Framework to Correct for Heritable Pathogen Effects on Infectious Disease Traits

التفاصيل البيبلوغرافية
العنوان: A Phylogeny-aware GWAS Framework to Correct for Heritable Pathogen Effects on Infectious Disease Traits
المؤلفون: Nadeau, Sarah, Thorball, Christian W, Kouyos, Roger, Günthard, Huldrych F, Böni, Jürg, Yerly, Sabine, Perreau, Matthieu, Klimkait, Thomas, Rauch, Andri, Hirsch, Hans H, Cavassini, Matthias, Vernazza, Pietro, Bernasconi, Enos, Fellay, Jacques, Mitov, Venelin, Stadler, Tanja, Swiss HIV Cohort Study (SHCS)
المساهمون: University of Zurich, Stadler, Tanja
المصدر: Molecular Biology and Evolution, 39 (8)
بيانات النشر: ETH Zurich, 2022.
سنة النشر: 2022
مصطلحات موضوعية: 10028 Institute of Medical Virology, 10234 Clinic for Infectious Diseases, phylogenetic mixed model, 1105 Ecology, Evolution, Behavior and Systematics, genome-wide association study, 1311 Genetics, infectious disease, 1312 Molecular Biology, 570 Life sciences, biology, 610 Medicine & health, heritability
الوصف: Infectious diseases are particularly challenging for genome-wide association studies (GWAS) because genetic effects from two organisms (pathogen and host) can influence a trait. Traditional GWAS assume individual samples are independent observations. However, pathogen effects on a trait can be heritable from donor to recipient in transmission chains. Thus, residuals in GWAS association tests for host genetic effects may not be independent due to shared pathogen ancestry. We propose a new method to estimate and remove heritable pathogen effects on a trait based on the pathogen phylogeny prior to host GWAS, thus restoring independence of samples. In simulations, we show this additional step can increase GWAS power to detect truly associated host variants when pathogen effects are highly heritable, with strong phylogenetic correlations. We applied our framework to data from two different host-pathogen systems, HIV in humans and X. arboricola in A. thaliana. In both systems, the heritability and thus phylogenetic correlations turn out to be low enough such that qualitative results of GWAS do not change when accounting for the pathogen shared ancestry through a correction step. This means that previous GWAS results applied to these two systems should not be biased due to shared pathogen ancestry. In summary, our framework provides additional information on the evolutionary dynamics of traits in pathogen populations and may improve GWAS if pathogen effects are highly phylogenetically correlated amongst individuals in a cohort.
Molecular Biology and Evolution, 39 (8)
ISSN:0737-4038
ISSN:1537-1719
وصف الملف: ZORA_227082.pdf - application/pdf; application/application/pdf
اللغة: English
تدمد: 0737-4038
1537-1719
DOI: 10.3929/ethz-b-000565801
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::171be269bdbe420f7dfbc5a00ae29ac8Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....171be269bdbe420f7dfbc5a00ae29ac8
قاعدة البيانات: OpenAIRE
الوصف
تدمد:07374038
15371719
DOI:10.3929/ethz-b-000565801