An evolutionary-network model reveals stratified interactions in the V3 loop of the HIV-1 envelope

• Published in: PLoS computational biology 2007-11, Vol.3 (11), p.e231-e231
• Main Authors: Poon, Art F Y, Lewis, Fraser I, Pond, Sergei L Kosakovsky, Frost, Simon D W
• Format: Article
• Language: English
• Subjects: Acquired immune deficiency syndrome; AIDS; Computational Biology; Evolution, Molecular; Evolutionary Biology; HIV; HIV-1 - chemistry; HIV-1 - genetics; Human immunodeficiency virus; Human immunodeficiency virus 1; Models, Genetic; Mutation; Phylogeny; Protein Conformation; Protein Structure, Tertiary; Proteins; Sequence Analysis - methods; Structure-Activity Relationship; Viral Envelope Proteins - chemistry; Viral Envelope Proteins - genetics; Virology; Viruses
• ISSN: 1553-7358; 1553-734X; 1553-7358
• DOI: 10.1371/journal.pcbi.0030231

The third variable loop (V3) of the human immunodeficiency virus type 1 (HIV-1) envelope is a principal determinant of antibody neutralization and progression to AIDS. Although it is undoubtedly an important target for vaccine research, extensive genetic variation in V3 remains an obstacle to the development of an effective vaccine. Comparative methods that exploit the abundance of sequence data can detect interactions between residues of rapidly evolving proteins such as the HIV-1 envelope, revealing biological constraints on their variability. However, previous studies have relied implicitly on two biologically unrealistic assumptions: (1) that founder effects in the evolutionary history of the sequences can be ignored, and; (2) that statistical associations between residues occur exclusively in pairs. We show that comparative methods that neglect the evolutionary history of extant sequences are susceptible to a high rate of false positives (20%-40%). Therefore, we propose a new method to detect interactions that relaxes both of these assumptions. First, we reconstruct the evolutionary history of extant sequences by maximum likelihood, shifting focus from extant sequence variation to the underlying substitution events. Second, we analyze the joint distribution of substitution events among positions in the sequence as a Bayesian graphical model, in which each branch in the phylogeny is a unit of observation. We perform extensive validation of our models using both simulations and a control case of known interactions in HIV-1 protease, and apply this method to detect interactions within V3 from a sample of 1,154 HIV-1 envelope sequences. Our method greatly reduces the number of false positives due to founder effects, while capturing several higher-order interactions among V3 residues. By mapping these interactions to a structural model of the V3 loop, we find that the loop is stratified into distinct evolutionary clusters. We extend our model to detect interactions between the V3 and C4 domains of the HIV-1 envelope, and account for the uncertainty in mapping substitutions to the tree with a parametric bootstrap.