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PhageLeads: Rapid Assessment of Phage Therapeutic Suitability Using an Ensemble Machine Learning Approach

Authors :
Kumarasan Yukgehnaish
Heera Rajandas
Sivachandran Parimannan
Ravichandran Manickam
Kasi Marimuthu
Bent Petersen
Martha R. J. Clokie
Andrew Millard
Thomas Sicheritz-Pontén
Source :
Viruses, Vol 14, Iss 2, p 342 (2022)
Publication Year :
2022
Publisher :
MDPI AG, 2022.

Abstract

The characterization of therapeutic phage genomes plays a crucial role in the success rate of phage therapies. There are three checkpoints that need to be examined for the selection of phage candidates, namely, the presence of temperate markers, antimicrobial resistance (AMR) genes, and virulence genes. However, currently, no single-step tools are available for this purpose. Hence, we have developed a tool capable of checking all three conditions required for the selection of suitable therapeutic phage candidates. This tool consists of an ensemble of machine-learning-based predictors for determining the presence of temperate markers (integrase, Cro/CI repressor, immunity repressor, DNA partitioning protein A, and antirepressor) along with the integration of the ABRicate tool to determine the presence of antibiotic resistance genes and virulence genes. Using the biological features of the temperate markers, we were able to predict the presence of the temperate markers with high MCC scores (>0.70), corresponding to the lifestyle of the phages with an accuracy of 96.5%. Additionally, the screening of 183 lytic phage genomes revealed that six phages were found to contain AMR or virulence genes, showing that not all lytic phages are suitable to be used for therapy. The suite of predictors, PhageLeads, along with the integrated ABRicate tool, can be accessed online for in silico selection of suitable therapeutic phage candidates from single genome or metagenomic contigs.

Details

Language :
English
ISSN :
19994915
Volume :
14
Issue :
2
Database :
Directory of Open Access Journals
Journal :
Viruses
Publication Type :
Academic Journal
Accession number :
edsdoj.94651bdb4b54fd196767dd3318c9bec
Document Type :
article
Full Text :
https://doi.org/10.3390/v14020342