Biology

Document Type

Article

Abstract

Metagenomic sequencing has greatly enhanced the discovery of viral genomic sequences; however, it remains challenging to identify the host(s) of these new viruses. We developed VirHostMatcher-Net, a flexible, network-based, Markov random field framework for predicting virus–prokaryote interactions using multiple, integrated features: CRISPR sequences and alignment-free similarity measures (s2∗ and WIsH). Evaluation of this method on a benchmark set of 1462 known virus–prokaryote pairs yielded host prediction accuracy of 59% and 86% at the genus and phylum levels, representing 16–27% and 6–10% improvement, respectively, over previous single-feature prediction approaches. We applied our host prediction tool to crAssphage, a human gut phage, and two metagenomic virus datasets: marine viruses and viral contigs recovered from globally distributed, diverse habitats. Host predictions were frequently consistent with those of previous studies, but more importantly, this new tool made many more confident predictions than previous tools, up to nearly 3-fold more (n > 27 000), greatly expanding the diversity of known virus–host interactions.

Publication Title

NAR Genomics and Bioinformatics

Publication Date

6-1-2020

Volume

2

Issue

2

ISSN

2631-9268

DOI

10.1093/nargab/lqaa044

Keywords

bacteriophage, clustered regularly interspaced short palindromic repeat; gastrointestinal tract; habitat; human; Markov random field, metagenomics, nonhuman, phylum, prediction, prokaryote, virus cell interaction

Cross Post Location

Student Publications

Creative Commons License

Creative Commons Attribution-NonCommercial 4.0 International License
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License

Included in

Biology Commons

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