Sequence Imputation of HPV16 Genomes for Genetic Association Studies

• Published in: PloS one Vol. 6; no. 6; p. e21375
• Main Authors: Smith, Benjamin, Chen, Zigui, Reimers, Laura, van Doorslaer, Koenraad, Schiffman, Mark, DeSalle, Rob, Herrero, Rolando, Yu, Kai, Wacholder, Sholom, Wang, Tao, Burk, Robert D.
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 23.06.2011; Public Library of Science (PLoS)
• Subjects: Algorithms; Analysis; Base Sequence; Bioinformatics; Biology; Biopsy; Cancer; Case-Control Studies; Cervical cancer; Chromosomes; Deoxyribonucleic acid; Diagnostic systems; DNA; Epidemiology; Evolution; Female; Gene sequencing; Genetic aspects; Genetic Association Studies; Genetic diversity; Genetic Predisposition to Disease; Genetic Variation; Genetics; Genome, Viral - genetics; Genome-wide association studies; Genome-Wide Association Study; Genomes; Genomics; Gynecology; Health aspects; Human papillomavirus; Human papillomavirus 16 - genetics; Human papillomavirus 16 - isolation & purification; Humans; Immunology; Infections; Medicine; Mutation; Nucleotide sequence; Nucleotides; Obstetrics; Papillomavirus infections; Pathogenicity; Pathogens; Pediatrics; Phylogenetics; Phylogeny; Polymerase chain reaction; Polymorphism, Single Nucleotide - genetics; Population; Recombination; Reference Standards; Sequence Analysis, DNA - methods; Single nucleotide polymorphisms; Single-nucleotide polymorphism; Stochasticity; Studies; Virology; Womens health; New York; United States > US; Maryland
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0021375

Human Papillomavirus type 16 (HPV16) causes over half of all cervical cancer and some HPV16 variants are more oncogenic than others. The genetic basis for the extraordinary oncogenic properties of HPV16 compared to other HPVs is unknown. In addition, we neither know which nucleotides vary across and within HPV types and lineages, nor which of the single nucleotide polymorphisms (SNPs) determine oncogenicity. A reference set of 62 HPV16 complete genome sequences was established and used to examine patterns of evolutionary relatedness amongst variants using a pairwise identity heatmap and HPV16 phylogeny. A BLAST-based algorithm was developed to impute complete genome data from partial sequence information using the reference database. To interrogate the oncogenic risk of determined and imputed HPV16 SNPs, odds-ratios for each SNP were calculated in a case-control viral genome-wide association study (VWAS) using biopsy confirmed high-grade cervix neoplasia and self-limited HPV16 infections from Guanacaste, Costa Rica. HPV16 variants display evolutionarily stable lineages that contain conserved diagnostic SNPs. The imputation algorithm indicated that an average of 97.5±1.03% of SNPs could be accurately imputed. The VWAS revealed specific HPV16 viral SNPs associated with variant lineages and elevated odds ratios; however, individual causal SNPs could not be distinguished with certainty due to the nature of HPV evolution. Conserved and lineage-specific SNPs can be imputed with a high degree of accuracy from limited viral polymorphic data due to the lack of recombination and the stochastic mechanism of variation accumulation in the HPV genome. However, to determine the role of novel variants or non-lineage-specific SNPs by VWAS will require direct sequence analysis. The investigation of patterns of genetic variation and the identification of diagnostic SNPs for lineages of HPV16 variants provides a valuable resource for future studies of HPV16 pathogenicity.