Evidence map›Paper›PMID 35921544›Full record

ArticleMolecular biology and evolution2022

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

Sarah Nadeau, Christian W Thorball, Roger Kouyos, Huldrych F Günthard, Jürg Böni, Sabine Yerly, Matthieu Perreau, Thomas Klimkait, Andri Rauch, Hans H Hirsch and 7 more

Abstract read
In one paragraph

Article in Molecular biology and evolution, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

17 authors.

Sarah NadeauDepartment of Biosystems Science and Engineering, ETH Zürich, Basel, Switzerland.ORCID 0000-0003-1008-8918
Christian W ThorballPrecision Medicine Unit, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
Roger KouyosInstitute of Medical Virology, University of Zurich, Zurich, Switzerland.
Huldrych F GünthardInstitute of Medical Virology, University of Zurich, Zurich, Switzerland.
Jürg BöniInstitute of Medical Virology, University of Zurich, Zurich, Switzerland.
Sabine YerlyDivision of Infectious Diseases, Laboratory of Virology, Geneva University Hospital, Geneva, Switzerland.
Matthieu PerreauDivision of Immunology and Allergy, University Hospital Lausanne, Lausanne, Switzerland.
Thomas KlimkaitDepartment of Biomedicine, University of Basel, Basel, Switzerland.
Andri RauchDepartment of Infectious Diseases, Bern University Hospital and University of Bern, Bern, Switzerland.
Hans H HirschDepartment of Biomedicine, University of Basel, Basel, Switzerland.ORCID 0000-0003-0883-0423
Matthias CavassiniDivision of Infectious Diseases, University Hospital Lausanne, Lausanne, Switzerland.ORCID 0000-0003-0933-7833
Pietro VernazzaDivision of Infectious Diseases, Cantonal Hospital St. Gallen, St. Gallen, Switzerland.
Enos BernasconiDivision of Infectious Diseases, Regional Hospital Lugano, Lugano, Switzerland.
Jacques FellaySwiss Institute of Bioinformatics, Lausanne, Switzerland.
Venelin MitovDepartment of Biosystems Science and Engineering, ETH Zürich, Basel, Switzerland.ORCID 0000-0002-5227-5191
Tanja StadlerDepartment of Biosystems Science and Engineering, ETH Zürich, Basel, Switzerland.ORCID 0000-0001-6431-535X
Swiss HIV Cohort Study (SHCS)

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

Communicable DiseasesGenome-Wide Association StudyHumansPhenotypePhylogenyPolymorphism, Single NucleotideQuantitative Trait, Heritablegenome-wide association studyheritabilityinfectious diseasephylogenetic mixed model

Identifiers

PMID35921544
PMCPMC9366186

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.