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

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 ge...

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Autores principales: Yukgehnaish, Kumarasan, Rajandas, Heera, Parimannan, Sivachandran, Manickam, Ravichandran, Marimuthu, Kasi, Petersen, Bent, Clokie, Martha R. J., Millard, Andrew, Sicheritz-Pontén, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8879740/
https://www.ncbi.nlm.nih.gov/pubmed/35215934
http://dx.doi.org/10.3390/v14020342
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author Yukgehnaish, Kumarasan
Rajandas, Heera
Parimannan, Sivachandran
Manickam, Ravichandran
Marimuthu, Kasi
Petersen, Bent
Clokie, Martha R. J.
Millard, Andrew
Sicheritz-Pontén, Thomas
author_facet Yukgehnaish, Kumarasan
Rajandas, Heera
Parimannan, Sivachandran
Manickam, Ravichandran
Marimuthu, Kasi
Petersen, Bent
Clokie, Martha R. J.
Millard, Andrew
Sicheritz-Pontén, Thomas
author_sort Yukgehnaish, Kumarasan
collection PubMed
description 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.
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spelling pubmed-88797402022-02-26 PhageLeads: Rapid Assessment of Phage Therapeutic Suitability Using an Ensemble Machine Learning Approach Yukgehnaish, Kumarasan Rajandas, Heera Parimannan, Sivachandran Manickam, Ravichandran Marimuthu, Kasi Petersen, Bent Clokie, Martha R. J. Millard, Andrew Sicheritz-Pontén, Thomas Viruses Article 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. MDPI 2022-02-08 /pmc/articles/PMC8879740/ /pubmed/35215934 http://dx.doi.org/10.3390/v14020342 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Yukgehnaish, Kumarasan
Rajandas, Heera
Parimannan, Sivachandran
Manickam, Ravichandran
Marimuthu, Kasi
Petersen, Bent
Clokie, Martha R. J.
Millard, Andrew
Sicheritz-Pontén, Thomas
PhageLeads: Rapid Assessment of Phage Therapeutic Suitability Using an Ensemble Machine Learning Approach
title PhageLeads: Rapid Assessment of Phage Therapeutic Suitability Using an Ensemble Machine Learning Approach
title_full PhageLeads: Rapid Assessment of Phage Therapeutic Suitability Using an Ensemble Machine Learning Approach
title_fullStr PhageLeads: Rapid Assessment of Phage Therapeutic Suitability Using an Ensemble Machine Learning Approach
title_full_unstemmed PhageLeads: Rapid Assessment of Phage Therapeutic Suitability Using an Ensemble Machine Learning Approach
title_short PhageLeads: Rapid Assessment of Phage Therapeutic Suitability Using an Ensemble Machine Learning Approach
title_sort phageleads: rapid assessment of phage therapeutic suitability using an ensemble machine learning approach
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8879740/
https://www.ncbi.nlm.nih.gov/pubmed/35215934
http://dx.doi.org/10.3390/v14020342
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