Unmasking the tissue-resident eukaryotic DNA virome in humans

Author:

Pyöriä Lari1ORCID,Pratas Diogo123ORCID,Toppinen Mari4ORCID,Hedman Klaus1ORCID,Sajantila Antti45ORCID,Perdomo Maria F1ORCID

Affiliation:

1. Department of Virology, University of Helsinki and Helsinki University Hospital , Helsinki  00290, Finland

2. Department of Electronics, Telecommunications and Informatics, University of Aveiro , Aveiro  3810-193, Portugal

3. Institute of Electronics and Informatics Engineering of Aveiro, University of Aveiro , Aveiro  3810-193, Portugal

4. Department of Forensic Medicine, University of Helsinki , Helsinki  00290, Finland

5. Forensic Medicine Unit, Finnish Institute for Health and Welfare , Helsinki  00271, Finland

Abstract

Abstract Little is known on the landscape of viruses that reside within our cells, nor on the interplay with the host imperative for their persistence. Yet, a lifetime of interactions conceivably have an imprint on our physiology and immune phenotype. In this work, we revealed the genetic make-up and unique composition of the known eukaryotic human DNA virome in nine organs (colon, liver, lung, heart, brain, kidney, skin, blood, hair) of 31 Finnish individuals. By integration of quantitative (qPCR) and qualitative (hybrid-capture sequencing) analysis, we identified the DNAs of 17 species, primarily herpes-, parvo-, papilloma- and anello-viruses (>80% prevalence), typically persisting in low copies (mean 540 copies/ million cells). We assembled in total 70 viral genomes (>90% breadth coverage), distinct in each of the individuals, and identified high sequence homology across the organs. Moreover, we detected variations in virome composition in two individuals with underlying malignant conditions. Our findings reveal unprecedented prevalences of viral DNAs in human organs and provide a fundamental ground for the investigation of disease correlates. Our results from post-mortem tissues call for investigation of the crosstalk between human DNA viruses, the host, and other microbes, as it predictably has a significant impact on our health.

Funder

Finnish Medical Foundation

Alfred Kordelin Foundation

Finnish Cultural Foundation

Orion Research Foundation

Emil Aaltonen Foundation

Finnish-Norwegian Medical Foundation

Instrumentarium Science Foundation

Biomedicum Helsinki Foundation

Helsinki University Hospital Research and Education Fund

Medical Society of Finland

Magnus Ehrnrooth Foundation

Jane and Aatos Erkko Foundation

Sigrid Jusé�lius Foundation

Life and Health Medical Foundation

Finnish Society of Sciences and Letters

Kone Foundation

Academy of Finland

Fundação para a Ciência e a Tecnologia

Publisher

Oxford University Press (OUP)

Subject

Genetics

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