Abstract

BackgroundAn increasing number of biological and clinical evidences have indicated that the microorganisms significantly get involved in the pathological mechanism of extensive varieties of complex human diseases. Inferring potential related microbes for diseases can not only promote disease prevention, diagnosis and treatment, but also provide valuable information for drug development. Considering that experimental methods are expensive and time-consuming, developing computational methods is an alternative choice. However, most of existing methods are biased towards well-characterized diseases and microbes. Furthermore, existing computational methods are limited in predicting potential microbes for new diseases.ResultsHere, we developed a novel computational model to predict potential human microbe-disease associations (MDAs) based on Weighted Meta-Graph (WMGHMDA). We first constructed a heterogeneous information network (HIN) by combining the integrated microbe similarity network, the integrated disease similarity network and the known microbe-disease bipartite network. And then, we implemented iteratively pre-designed Weighted Meta-Graph search algorithm on the HIN to uncover possible microbe-disease pairs by cumulating the contribution values of weighted meta-graphs to the pairs as their probability scores. Depending on contribution potential, we described the contribution degree of different types of meta-graphs to a microbe-disease pair with bias rating. Meta-graph with higher bias rating will be assigned greater weight value when calculating probability scores.ConclusionsThe experimental results showed that WMGHMDA outperformed some state-of-the-art methods with average AUCs of 0.9288, 0.9068 ±0.0031 in global leave-one-out cross validation (LOOCV) and 5-fold cross validation (5-fold CV), respectively. In the case studies, 9, 19, 37 and 10, 20, 45 out of top-10, 20, 50 candidate microbes were manually verified by previous reports for asthma and inflammatory bowel disease (IBD), respectively. Furthermore, three common human diseases (Crohn’s disease, Liver cirrhosis, Type 1 diabetes) were adopted to demonstrate that WMGHMDA could be efficiently applied to make predictions for new diseases. In summary, WMGHMDA has a high potential in predicting microbe-disease associations.

Highlights

  • An increasing number of biological and clinical evidences have indicated that the microorganisms significantly get involved in the pathological mechanism of extensive varieties of complex human diseases

  • We proposed a novel computational model of WMGHMDA for inferring candidate microbes for diseases on heterogeneous information network (HIN) based on Weighted Meta-Graph

  • In the framework of leave-one-out cross validation (LOOCV), each observed microbe-disease pair is selected as test sample in turn while the rest observed microbe-disease association pairs are considered as training samples

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Summary

Introduction

An increasing number of biological and clinical evidences have indicated that the microorganisms significantly get involved in the pathological mechanism of extensive varieties of complex human diseases. It is reported that there exist about 1014 microorganism cells inhabiting an adult intestine, which is approximately 10 times more than human cells [3] These cells could produce a large amount of gene product which is essential for various metabolic and biochemical activities [4, 5]. The dynamic changes of these factors can lead to the imbalance of microbial communities and further affect the biological progress (i.e., metabolism, proteomic) of associated microbes, which possibly motivates a variety of important human diseases, such as asthma [14], diabetes [15], liver diseases [16], and even cancer [17]

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