Key result
The proposed profile HMM-based mutual information kernel was substantially more powerful than competing kernels in identifying protein sequence segments associated with HIV-1 neutralizing antibody resistance.
A novel kernel-based logistic regression model improves the power to analyze complex protein sequence data in vaccine research.
May advance HIV vaccine sequence analysis; hypothesis-generating pending independent validation.
Protein sequence data arise more and more often in vaccine and infectious disease research. These types of data are discrete, high-dimensional, and complex. We propose to study the impact of protein sequences on binary outcomes using a kernel-based logistic regression model, which models the effect of protein through a random effect whose variance-covariance matrix is mostly determined by a kernel function. We propose a novel, biologically motivated, profile hidden Markov model (HMM)-based mutual information (MI) kernel. Hypothesis testing can be carried out using the maximum of the score statistics and a parametric bootstrap procedure. To improve the power of testing, we propose intuitive modifications to the test statistic. We show through simulation studies that the profile HMM-based MI kernel can be substantially more powerful than competing kernels, and that the modified test statistics bring incremental gains in power. We use these proposed methods to investigate two problems from HIV-1 vaccine research: (1) identifying segments of HIV-1 envelope (Env) protein that confer resistance to neutralizing antibody and (2) identifying segments of Env that are associated with attenuation of protective vaccine effect by antibodies of isotype A in the RV144 vaccine trial.
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Fong et al. (2014) studied HIV-1 (n=32). Kernel-based logistic regression model with profile HMM MI kernel vs. Radial basis function (RBF) kernels was evaluated on Association between protein sequence variation and binary outcomes (e.g., antibody resistance). The proposed profile HMM-based mutual information kernel was substantially more powerful than competing kernels in identifying protein sequence segments associated with HIV-1 neutralizing antibody resistance.
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