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BacARscan: an in silico resource to discern diversity in antibiotic resistance genes

Antibiotic resistance has escalated as a significant problem of broad public health significance. Regular surveillance of antibiotic resistance genes (ARGs) in microbes and metagenomes from human, animal and environmental sources is vital to understanding ARGs’ epidemiology and foreseeing the emerge...

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Autores principales: Pandey, Deeksha, Kumari, Bandana, Singhal, Neelja, Kumar, Manish
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9722225/
https://www.ncbi.nlm.nih.gov/pubmed/36479434
http://dx.doi.org/10.1093/biomethods/bpac031
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author Pandey, Deeksha
Kumari, Bandana
Singhal, Neelja
Kumar, Manish
author_facet Pandey, Deeksha
Kumari, Bandana
Singhal, Neelja
Kumar, Manish
author_sort Pandey, Deeksha
collection PubMed
description Antibiotic resistance has escalated as a significant problem of broad public health significance. Regular surveillance of antibiotic resistance genes (ARGs) in microbes and metagenomes from human, animal and environmental sources is vital to understanding ARGs’ epidemiology and foreseeing the emergence of new antibiotic resistance determinants. Whole-genome sequencing (WGS)-based identification of the microbial ARGs using antibiotic resistance databases and in silico prediction tools can significantly expedite the monitoring and characterization of ARGs in various niches. The major hindrance to the annotation of ARGs from WGS data is that most genome databases contain fragmented genes/genomes (due to incomplete assembly). Herein, we describe an insilicoBacterial Antibiotic Resistance scan (BacARscan) (http://proteininformatics.org/mkumar/bacarscan/) that can detect, predict and characterize ARGs in -omics datasets, including short sequencing, reads, and fragmented contigs. Benchmarking on an independent non-redundant dataset revealed that the performance of BacARscan was better than other existing methods, with nearly 92% Precision and 95% F-measure on a combined dataset of ARG and non-ARG proteins. One of the most notable improvements of BacARscan over other ARG annotation methods is its ability to work on genomes and short-reads sequence libraries with equal efficiency and without any requirement for assembly of short reads. Thus, BacARscan can help monitor the prevalence and diversity of ARGs in microbial populations and metagenomic samples from animal, human, and environmental settings. The authors intend to constantly update the current version of BacARscan as and when new ARGs are discovered. Executable versions, source codes, sequences used for development and usage instructions are available at (http://www.proteininformatics.org/mkumar/bacarscan/downloads.html) and GitHub repository (https://github.com/mkubiophysics/BacARscan).
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spelling pubmed-97222252022-12-06 BacARscan: an in silico resource to discern diversity in antibiotic resistance genes Pandey, Deeksha Kumari, Bandana Singhal, Neelja Kumar, Manish Biol Methods Protoc Methods Article Antibiotic resistance has escalated as a significant problem of broad public health significance. Regular surveillance of antibiotic resistance genes (ARGs) in microbes and metagenomes from human, animal and environmental sources is vital to understanding ARGs’ epidemiology and foreseeing the emergence of new antibiotic resistance determinants. Whole-genome sequencing (WGS)-based identification of the microbial ARGs using antibiotic resistance databases and in silico prediction tools can significantly expedite the monitoring and characterization of ARGs in various niches. The major hindrance to the annotation of ARGs from WGS data is that most genome databases contain fragmented genes/genomes (due to incomplete assembly). Herein, we describe an insilicoBacterial Antibiotic Resistance scan (BacARscan) (http://proteininformatics.org/mkumar/bacarscan/) that can detect, predict and characterize ARGs in -omics datasets, including short sequencing, reads, and fragmented contigs. Benchmarking on an independent non-redundant dataset revealed that the performance of BacARscan was better than other existing methods, with nearly 92% Precision and 95% F-measure on a combined dataset of ARG and non-ARG proteins. One of the most notable improvements of BacARscan over other ARG annotation methods is its ability to work on genomes and short-reads sequence libraries with equal efficiency and without any requirement for assembly of short reads. Thus, BacARscan can help monitor the prevalence and diversity of ARGs in microbial populations and metagenomic samples from animal, human, and environmental settings. The authors intend to constantly update the current version of BacARscan as and when new ARGs are discovered. Executable versions, source codes, sequences used for development and usage instructions are available at (http://www.proteininformatics.org/mkumar/bacarscan/downloads.html) and GitHub repository (https://github.com/mkubiophysics/BacARscan). Oxford University Press 2022-11-30 /pmc/articles/PMC9722225/ /pubmed/36479434 http://dx.doi.org/10.1093/biomethods/bpac031 Text en © The Author(s) 2022. Published by Oxford University Press. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Methods Article
Pandey, Deeksha
Kumari, Bandana
Singhal, Neelja
Kumar, Manish
BacARscan: an in silico resource to discern diversity in antibiotic resistance genes
title BacARscan: an in silico resource to discern diversity in antibiotic resistance genes
title_full BacARscan: an in silico resource to discern diversity in antibiotic resistance genes
title_fullStr BacARscan: an in silico resource to discern diversity in antibiotic resistance genes
title_full_unstemmed BacARscan: an in silico resource to discern diversity in antibiotic resistance genes
title_short BacARscan: an in silico resource to discern diversity in antibiotic resistance genes
title_sort bacarscan: an in silico resource to discern diversity in antibiotic resistance genes
topic Methods Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9722225/
https://www.ncbi.nlm.nih.gov/pubmed/36479434
http://dx.doi.org/10.1093/biomethods/bpac031
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