UMMS Affiliation

Department of Medicine, Division of Infectious Diseases and Immunology

Date

9-15-2011

Document Type

Article

Subjects

2',5'-Oligoadenylate Synthetase; Female; GTP-Binding Proteins; Genetic Predisposition to Disease; Haplotypes; Humans; Interferon Regulatory Factor-3; Male; Middle Aged; Polymorphism, Single Nucleotide; West Nile Fever

Disciplines

Life Sciences | Medicine and Health Sciences | Women's Studies

Abstract

West Nile virus (WNV), a category B pathogen endemic in parts of Africa, Asia and Europe, emerged in North America in 1999, and spread rapidly across the continental U.S. Outcomes of infection with WNV range from asymptomatic to severe neuroinvasive disease manifested as encephalitis, paralysis, and/or death. Neuroinvasive WNV disease occurs in less than one percent of cases, and although host genetic factors are thought to influence risk for symptomatic disease, the identity of these factors remains largely unknown. We tested 360 common haplotype tagging and/or functional SNPs in 86 genes that encode key regulators of immune function in 753 individuals infected with WNV including: 422 symptomatic WNV cases and 331 cases with asymptomatic infections. After applying a Bonferroni correction for multiple tests and controlling for population stratification, SNPs in IRF3 (OR 0.54, p = 0.035) and MX1, (OR 0.19, p = 0.014) were associated with symptomatic WNV infection and a single SNP in OAS1 (OR 9.79, p = 0.003) was associated with increased risk for West Nile encephalitis and paralysis (WNE/P). Together, these results suggest that genetic variation in the interferon response pathway is associated with both risk for symptomatic WNV infection and WNV disease progression.

Rights and Permissions

Citation: PLoS One. 2011;6(9):e24745. Epub 2011 Sep 15. Link to article on publisher's site

Related Resources

Link to Article in PubMed

PubMed ID

21935451

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