Bayesian modeling of co-occurrence microbial interaction networks

The human body consists of microbiomes associated with the development and prevention of several diseases. These microbial organisms form several complex interactions that are informative to the scientific community for explaining disease progression and prevention. Contrary to the traditional view of the microbiome as a singular, assortative network, we introduce a novel statistical approach using a weighted stochastic infinite block model to analyze the complex community structures within microbial co-occurrence microbial interaction networks. Our model defines connections between microbial taxa using a novel semi-parametric rank-based correlation method on their transformed relative abundances within a fully connected network framework. Employing a Bayesian nonparametric approach, the proposed model effectively clusters taxa into distinct communities while estimating the number of communities. The posterior summary of the taxa community membership is obtained based on the posterior probability matrix, which could naturally solve the label switching problem. Through simulation studies and real-world application to microbiome data from postmenopausal patients with recurrent urinary tract infections, we demonstrate that our method has superior clustering accuracy over alternative approaches. This advancement provides a more nuanced understanding of microbiome organization, with significant implications for disease research.
Comment: 25 pages