Computational Studies of Virus-host Interactions Using Metagenomics Data and Applications Summary: Viruses are ubiquitous in almost every ecological environment including the human body, water, soil, etc. They play important roles in the normal function of human microbiome. Many viruses have been shown to be associated with human diseases. However, our understanding of the roles of viruses in ecological communities is very limited. Recent technological and computational advances make it possible to have a deep understanding of the roles of viruses in public health and the environment. Metagenomics studies from various environments including the human microbiome projects (HMP), global ocean, and the earth microbiome projects have generated large amounts of short read data. Viruses are present in most of these metagenomic data sets and their hosts are unknown. In this proposal, the investigators will develop computational approaches for the identification of viral sequences from metagenomic data sets and for the study of virus-host interactions. For the identification of viral sequences from metagenomics samples, novel statistical measures using word patterns will first be developed. Second, a unified nave Bayesian integrative approach by combining information from word patterns, gene directionality, and gene annotation will be studied. Third, the identified viral sequences from metagenomes will be further assembled to construct complete viral genomes using a novel binning approach to be developed by the investigators. Finally, the remaining reads will be assigned to the corresponding bins. For the study of virus- host interactions, computational methods to estimate the reliability of virus-host interactions from high-throughput experiments will first be developed. Then machine learning approaches will be developed to predict viruses infecting certain hosts. Finally, a network logistic regression approach will be developed to predict virus-host interactions. These computational approaches for the identification of viral sequences and for predicting virus-host interactions will be applied to a public liver cirrhosis and a unique metagenomics data set to understand how metagenomes change with health status, identify viruses and virus-host interactions associated with disease status and accurately predict disease status using bacteria, viruses and virus-host interactions. The developed computational methods will also be used to analyze metageomic data from various locations based on the TARA ocean data and a unique time series data to understand how environmental factors affect virus abundance and virus-host interactions. Some of the predictions will be experimentally validated. Software derived from the proposal will be developed and freely distributed to the scientific community.

Public Health Relevance

Viruses are abundant in many environments and are important to public health. New statistical and computational tools will be developed for the identification of viral sequences from metagenomics samples and for the prediction of virus-host interactions. These tools will be used to analyze microbial data sets related to liver cirrhosis and travelers? diarrhea as well as marine metagenomics data sets from various geographic locations and time series.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
3R01GM120624-02S1
Application #
9704539
Study Section
Program Officer
Ravichandran, Veerasamy
Project Start
2017-04-15
Project End
2021-03-31
Budget Start
2018-04-01
Budget End
2019-03-31
Support Year
2
Fiscal Year
2018
Total Cost
Indirect Cost
Name
University of Southern California
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
072933393
City
Los Angeles
State
CA
Country
United States
Zip Code
90089
Li, Han; Sun, Fengzhu (2018) Comparative studies of alignment, alignment-free and SVM based approaches for predicting the hosts of viruses based on viral sequences. Sci Rep 8:10032
Tang, Kujin; Lu, Yang Young; Sun, Fengzhu (2018) Background Adjusted Alignment-Free Dissimilarity Measures Improve the Detection of Horizontal Gene Transfer. Front Microbiol 9:711
Lu, Yang Young; Lv, Jinchi; Fuhrman, Jed A et al. (2017) Towards enhanced and interpretable clustering/classification in integrative genomics. Nucleic Acids Res 45:e169
Ahlgren, Nathan A; Ren, Jie; Lu, Yang Young et al. (2017) Alignment-free $d_2^*$ oligonucleotide frequency dissimilarity measure improves prediction of hosts from metagenomically-derived viral sequences. Nucleic Acids Res 45:39-53
Wang, Ying; Wang, Kun; Lu, Yang Young et al. (2017) Improving contig binning of metagenomic data using [Formula: see text] oligonucleotide frequency dissimilarity. BMC Bioinformatics 18:425
Ren, Jie; Ahlgren, Nathan A; Lu, Yang Young et al. (2017) VirFinder: a novel k-mer based tool for identifying viral sequences from assembled metagenomic data. Microbiome 5:69
Lu, Yang Young; Tang, Kujin; Ren, Jie et al. (2017) CAFE: aCcelerated Alignment-FrEe sequence analysis. Nucleic Acids Res 45:W554-W559