Viral Genetic Determinants of Prolonged Respiratory Syncytial Virus Infection Among Infants in a Healthy Term Birth Cohort

Author:

Lawless Dylan1ORCID,McKennan Christopher G2,Das Suman R3,Junier Thomas4,Xu Zhi Ming1,Anderson Larry J5,Gebretsadik Tebeb6,Shilts Meghan H7,Larkin Emma8,Rosas-Salazar Christian9,Chappell James D9,Fellay Jacques110,Hartert Tina V79

Affiliation:

1. Global Health Institute, School of Life Sciences, Ecole Polytechnique Fédérale de Lausanne , Lausanne , Switzerland

2. Department of Statistics, University of Pittsburgh , Pittsburgh, Pennsylvania , USA

3. Division of Infectious Diseases, Department of Medicine, Vanderbilt University Medical Center , Nashville, Tennessee , USA

4. Swiss Institute of Bioinformatics, Vital-IT Group , Lausanne , Switzerland

5. Department of Pediatrics, Emory University School of Medicine and Children's Healthcare of Atlanta , Atlanta, Georgia , USA

6. Department of Biostatistics, Vanderbilt University Medical Center , Nashville, Tennessee , USA

7. Department of Medicine, Vanderbilt University Medical Center , Nashville, Tennessee , USA

8. Division of Allergy, Immunology, and Pulmonary and Critical Care Medicine, Department of Medicine, Vanderbilt University Medical Center , Nashville, Tennessee , USA

9. Department of Pediatrics, Vanderbilt University Medical Center , Nashville, Tennessee , USA

10. Biomedical Data Science Center, Lausanne University Hospital and University of Lausanne , Lausanne , Switzerland

Abstract

Abstract Background Respiratory syncytial virus (RSV) is associated with acute respiratory infection. We sought to identify RSV variants associated with prolonged infection. Methods Among healthy term infants we identified those with prolonged RSV infection and conducted (1) a human genome-wide association study (GWAS) to test the dependence of infection risk on host genotype, (2) a viral GWAS for association with prolonged RSV infection using RSV whole-genome sequencing, (3) an analysis of all viral public sequences, (4) an assessment of immunological responses, and (5) a summary of all major functional data. Analyses were adjusted for viral/human population structure and host factors associated with infection risk. Results We identified p.E123K/D and p.P218T/S/L in G protein that were associated with prolonged infection (Padj = .01). We found no evidence of host genetic risk for infection. The RSV variant positions approximate sequences that could bind a putative viral receptor, heparan sulfate. Conclusions Using analysis of both viral and host genetics we identified a novel RSV variant associated with prolonged infection in otherwise healthy infants and no evidence supporting host genetic susceptibility to infection. As the capacity of RSV for chronicity and its viral reservoir are not defined, these findings are important for understanding the impact of RSV on chronic disease and endemicity.

Funder

National Institutes of Health

Swiss National Science Foundation

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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