Association of SNP-SNP interactions of surfactant protein genes with severity of respiratory syncytial virus infection in children.

Abstract

The severity of respiratory syncytial virus (RSV) may be linked to host genetic susceptibility. Surfactant protein (SP) genetic variants have been associated with RSV severity, but the impact of SNP-SNP (single nucleotide polymorphism) interactions remains unexplored. Therefore, we employed a novel statistical model to investigate the association of SNP-SNP interactions of SFTP genes with RSV severity in two and three-interaction models. We analyzed available genotype and clinical data from prospectively enrolled 405 children diagnosed with RSV, categorizing them into moderate or severe RSV groups. Using Wang's statistical model, we studied significant associations of SNP-SNP interactions with RSV severity in a case-control design. We observed, 1) association of three interactions with increased risk of severe RSV in a two-SNP model. One intragenic interaction was between SNPs of SFTPA2, and the other two were intergenic, involving SNPs of hydrophilic and hydrophobic SPs alone. 2) association of 22 interactions with RSV severity in a three-SNP model. Among these, 20 were unique, with 12 and 10 interactions associated with increased or decreased risk of RSV severity, respectively, and included at least one SNP of either SFTPA1 or SFTPA2. All interactions were intergenic, except one among SNPs of SFTPA1. The remaining interactions were either among SNPs of hydrophilic SPs alone (n=8) or among SNPs of both hydrophilic or hydrophobic SPs (n=11). Our findings indicate that SNPs of all SFTPs may contribute to genetic susceptibility to RSV severity. However, the predominant involvement of SFTPA1 and/or SFTPA2 SNPs in these interactions underscores their significance in RSV severity.