Evidence map›Paper›PMID 35296232›Full record

ArticleBMC genomics2022

GBDR: a Bayesian model for precise prediction of pathogenic microorganisms using 16S rRNA gene sequences.

Yu-An Huang, Zhi-An Huang, Jian-Qiang Li, Zhu-Hong You, Lei Wang, Hai-Cheng Yi, Chang-Qing Yu

Open access · goldAbstract read
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Article in BMC genomics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

7 authors at 5 institutions in 2 countries.

Yu-An Huang *Department of Information Engineering, Xijing University, Xi'an, 710123, China. yahuang1991@gmail.com.
Zhi-An Huang *Center for Computer Science and Information Technology, City University of Hong Kong Dongguan Research Institute, Dongguan, China.
Jian-Qiang LiCollege of Computer Science and Software Engineering, Shenzhen University, Shenzhen, 518000, China. lijq@szu.edu.cn.
Zhu-Hong YouDepartment of Information Engineering, Xijing University, Xi'an, 710123, China.
Lei WangGuangxi Academy of Science, Nanning, 530000, China.
Hai-Cheng YiXinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Ürümqi, 830000, China.
Chang-Qing YuDepartment of Information Engineering, Xijing University, Xi'an, 710123, China.
Xijing University · CNChinese Academy of Sciences · CNCity University of Hong Kong · HKGuangxi Academy of Sciences · CNShenzhen University · CN

Funding

National Key RD Program of China 2020YFA0908700National Natural Science Foundation of China 61572506National Natural Science Foundation of China 61702424
6 · The paper itself

Abstract

backgroundRecent evidences have suggested that human microorganisms participate in important biological activities in the human body. The dysfunction of host-microbiota interactions could lead to complex human disorders. The knowledge on host-microbiota interactions can provide valuable insights into understanding the pathological mechanism of diseases. However, it is time-consuming and costly to identify the disorder-specific microbes from the biological "haystack" merely by routine wet-lab experiments. With the developments in next-generation sequencing and omics-based trials, it is imperative to develop computational prediction models for predicting microbe-disease associations on a large scale.

resultsBased on the known microbe-disease associations derived from the Human Microbe-Disease Association Database (HMDAD), the proposed model shows reliable performance with high values of the area under ROC curve (AUC) of 0.9456 and 0.8866 in leave-one-out cross validations and five-fold cross validations, respectively. In case studies of colorectal carcinoma, 80% out of the top-20 predicted microbes have been experimentally confirmed via published literatures.

conclusionBased on the assumption that functionally similar microbes tend to share the similar interaction patterns with human diseases, we here propose a group based computational model of Bayesian disease-oriented ranking to prioritize the most potential microbes associating with various human diseases. Based on the sequence information of genes, two computational approaches (BLAST+ and MEGA 7) are leveraged to measure the microbe-microbe similarity from different perspectives. The disease-disease similarity is calculated by capturing the hierarchy information from the Medical Subject Headings (MeSH) data. The experimental results illustrate the accuracy and effectiveness of the proposed model. This work is expected to facilitate the characterization and identification of promising microbial biomarkers.

Indexed as

AlgorithmsComputational BiologyRNA, Ribosomal, 16SBacteriaBayes TheoremGenes, rRNAHumansRNA, Ribosomal, 16S16S rRNA sequence analysisBayesian rankingComputational prediction modelMicrobe-disease association networkPathogenic microorganisms

Identifiers

PMID35296232
PMCPMC8925046
OpenAlexW4221128692

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