A Novel Approach Based on Bipartite Network Recommendation and KATZ Model to Predict Potential Micro-Disease Associations

Accumulating evidence indicates that the microbes colonizing human bodies have crucial effects on human health and the discovery of disease-related microbes will promote the discovery of biomarkers and drugs for the prevention, diagnosis, treatment, and prognosis of diseases. However clinical experiments of disease-microbe associations are time-consuming, laborious and expensive, and there are few methods for predicting potential microbe-disease association. Therefore, developing effective computational models utilizing the accumulated public data of clinically validated microbe-disease associations to identify novel disease-microbe associations is of practical importance. We propose a novel method based on the KATZ model and Bipartite Network Recommendation Algorithm (KATZBNRA) to discover potential associations between microbes and diseases. We calculate the Gaussian interaction profile kernel similarity of diseases and microbes based on validated disease-microbe associations. Then, we construct a bipartite graph and execute a bipartite network recommendation algorithm. Finally, we integrate the disease similarity, microbe similarity and bipartite network recommendation score to obtain the final score, which is used to infer whether there are some novel disease-microbe interactions. To evaluate the predictive power of KATZBNRA, we tested it with the walk length 2 using global leave-one-out cross validation (LOOV), two-fold and five-fold cross validations, with AUCs of 0.9098, 0.8463 and 0.8969, respectively. The test results also show that KATZBNRA is more accurate than two recent similar methods KATZHMDA and BNPMDA.

[1]  Lei Wang,et al.  BNPMDA: Bipartite Network Projection for MiRNA–Disease Association prediction , 2018, Bioinform..

[2]  L. Fry,et al.  Triggering psoriasis: the role of infections and medications. , 2007, Clinics in dermatology.

[3]  Feng Liu,et al.  Predicting potential drug-drug interactions by integrating chemical, biological, phenotypic and network data , 2017, BMC Bioinformatics.

[4]  Dean Billheimer,et al.  Asthma-associated differences in microbial composition of induced sputum. , 2013, The Journal of allergy and clinical immunology.

[5]  H. Ogata,et al.  Imbalance in intestinal microflora constitution could be involved in the pathogenesis of inflammatory bowel disease. , 2008, International journal of medical microbiology : IJMM.

[6]  Jack A Gilbert,et al.  Community ecology as a framework for human microbiome research , 2019, Nature Medicine.

[7]  J. Doré,et al.  Low counts of Faecalibacterium prausnitzii in colitis microbiota , 2009, Inflammatory bowel diseases.

[8]  Roded Sharan,et al.  Associating Genes and Protein Complexes with Disease via Network Propagation , 2010, PLoS Comput. Biol..

[9]  George M Weinstock,et al.  The relationships between environmental bacterial exposure, airway bacterial colonization, and asthma , 2014, Current opinion in allergy and clinical immunology.

[10]  Tanja Woyke,et al.  Airway microbiota and bronchial hyperresponsiveness in patients with suboptimally controlled asthma. , 2011, The Journal of allergy and clinical immunology.

[11]  Sang-Gue Park,et al.  Analysis of Oropharyngeal Microbiota between the Patients with Bronchial Asthma and the Non-Asthmatic Persons , 2013 .

[12]  Zejun Li,et al.  Human Microbe-Disease Association Prediction With Graph Regularized Non-Negative Matrix Factorization , 2018, Front. Microbiol..

[13]  Xiangxiang Zeng,et al.  Prediction of Potential Disease-Associated MicroRNAs by Using Neural Networks , 2019, Molecular therapy. Nucleic acids.

[14]  Zhu-Hong You,et al.  A novel approach based on KATZ measure to predict associations of human microbiota with non‐infectious diseases , 2016, Bioinform..

[15]  Xing Chen,et al.  Novel human lncRNA-disease association inference based on lncRNA expression profiles , 2013, Bioinform..

[16]  Elizabeth A. Grice,et al.  The skin microbiome , 2020, Nature.

[17]  Rui Gao,et al.  PRWHMDA: Human Microbe-Disease Association Prediction by Random Walk on the Heterogeneous Network with PSO , 2018, International journal of biological sciences.

[18]  Jingpu Zhang,et al.  A novel approach for predicting microbe-disease associations by bi-random walk on the heterogeneous network , 2017, PLoS ONE.

[19]  Elena Marchiori,et al.  Gaussian interaction profile kernels for predicting drug-target interaction , 2011, Bioinform..

[20]  L. Brandt,et al.  Fecal microbiota transplantation: past, present and future , 2013, Current opinion in gastroenterology.

[21]  Zhu-Hong You,et al.  FMSM: a novel computational model for predicting potential miRNA biomarkers for various human diseases , 2018, BMC Systems Biology.

[22]  B. T. Fein Bronchial asthma caused by Pseudomonas aeruginosa diagnosed by bronchoscopic examination. , 1955, Annals of allergy.

[23]  R. Knight,et al.  Meta‐analyses of human gut microbes associated with obesity and IBD , 2014, FEBS letters.

[24]  Byoung-Ju Kim,et al.  The Effects of Lactobacillus rhamnosus on the Prevention of Asthma in a Murine Model , 2010, Allergy, asthma & immunology research.

[25]  Taeko Dohi,et al.  Dysbiosis of Salivary Microbiota in Inflammatory Bowel Disease and Its Association With Oral Immunological Biomarkers , 2013, DNA research : an international journal for rapid publication of reports on genes and genomes.

[26]  Herman Goossens,et al.  Denaturing gradient gel electrophoresis of neonatal intestinal microbiota in relation to the development of asthma , 2011, BMC Microbiology.

[27]  Na-Na Guan,et al.  Predicting miRNA‐disease association based on inductive matrix completion , 2018, Bioinform..

[28]  De-Shuang Huang,et al.  Novel human microbe-disease association prediction using network consistency projection , 2017, BMC Bioinformatics.

[29]  Xiangxiang Zeng,et al.  Prediction of potential disease-associated microRNAs using structural perturbation method , 2017, bioRxiv.

[30]  F. Martinez,et al.  Genes, environments, development and asthma: a reappraisal , 2006, European Respiratory Journal.

[31]  Hailin Chen,et al.  Similarity-based methods for potential human microRNA-disease association prediction , 2013, BMC Medical Genomics.

[32]  Katherine H. Huang,et al.  Structure, Function and Diversity of the Healthy Human Microbiome , 2012, Nature.

[33]  Cheng Liang,et al.  KATZMDA: Prediction of miRNA-Disease Associations Based on KATZ Model , 2018, IEEE Access.

[34]  Fein Bt,et al.  Bronchial asthma caused by Pseudomonas aeruginosa diagnosed by bronchoscopic examination. , 1955 .

[35]  Peter G Gibson,et al.  Inhibition of allergic airways disease by immunomodulatory therapy with whole killed Streptococcus pneumoniae. , 2007, Vaccine.

[36]  Yi-Cheng Zhang,et al.  Bipartite network projection and personal recommendation. , 2007, Physical review. E, Statistical, nonlinear, and soft matter physics.

[37]  Feng Huang,et al.  Predicting drug-disease associations and their therapeutic function based on the drug-disease association bipartite network. , 2018, Methods.

[38]  Qi Zhao,et al.  HNGRNMF: Heterogeneous Network-based Graph Regularized Nonnegative Matrix Factorization for predicting events of microbe-disease associations , 2018, 2018 IEEE International Conference on Bioinformatics and Biomedicine (BIBM).

[39]  Jong-Wook Shin,et al.  Lung Microbiome Analysis in Steroid-Naїve Asthma Patients by Using Whole Sputum , 2016, Tuberculosis and respiratory diseases.

[40]  Feng Liu,et al.  Predicting drug-disease associations by using similarity constrained matrix factorization , 2018, BMC Bioinformatics.

[41]  M. Pop,et al.  Metagenomic Analysis of the Human Distal Gut Microbiome , 2006, Science.

[42]  Jun Wang,et al.  Metagenome-wide association studies: fine-mining the microbiome , 2016, Nature Reviews Microbiology.

[43]  Xing Chen KATZLDA: KATZ measure for the lncRNA-disease association prediction , 2015, Scientific Reports.

[44]  Fei Luo,et al.  The Bi-Direction Similarity Integration Method for Predicting Microbe-Disease Associations , 2018, IEEE Access.

[45]  M. Meyerson,et al.  Metagenomic Characterization of Microbial Communities In Situ Within the Deeper Layers of the Ileum in Crohn’s Disease , 2016, Cellular and molecular gastroenterology and hepatology.

[46]  I. Dobrić,et al.  Normalization in the appearance of severly damaged psoriatic nails using soft x-rays. A case report. , 2007, Acta dermatovenerologica Croatica : ADC.

[47]  D. R. Linden,et al.  Effects of gastrointestinal inflammation on enteroendocrine cells and enteric neural reflex circuits , 2006, Autonomic Neuroscience.

[48]  Xing Chen,et al.  FMLNCSIM: fuzzy measure-based lncRNA functional similarity calculation model , 2016, Oncotarget.

[49]  Xinghua Shi,et al.  A Network Based Method for Analysis of lncRNA-Disease Associations and Prediction of lncRNAs Implicated in Diseases , 2014, PloS one.

[50]  F. Bäckhed,et al.  The gut microbiota — masters of host development and physiology , 2013, Nature Reviews Microbiology.

[51]  R. Nomura,et al.  Aggravation of inflammatory bowel diseases by oral streptococci. , 2014, Oral diseases.