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BMScan: using whole genome similarity to rapidly and accurately identify bacterial meningitis causing species

BACKGROUND: Bacterial meningitis is a life-threatening infection that remains a public health concern. Bacterial meningitis is commonly caused by the following species: Neisseria meningitidis, Streptococcus pneumoniae, Listeria monocytogenes, Haemophilus influenzae and Escherichia coli. Here, we des...

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Autores principales: Topaz, Nadav, Boxrud, Dave, Retchless, Adam C., Nichols, Megan, Chang, How-Yi, Hu, Fang, Wang, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6094466/
https://www.ncbi.nlm.nih.gov/pubmed/30111301
http://dx.doi.org/10.1186/s12879-018-3324-1
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author Topaz, Nadav
Boxrud, Dave
Retchless, Adam C.
Nichols, Megan
Chang, How-Yi
Hu, Fang
Wang, Xin
author_facet Topaz, Nadav
Boxrud, Dave
Retchless, Adam C.
Nichols, Megan
Chang, How-Yi
Hu, Fang
Wang, Xin
author_sort Topaz, Nadav
collection PubMed
description BACKGROUND: Bacterial meningitis is a life-threatening infection that remains a public health concern. Bacterial meningitis is commonly caused by the following species: Neisseria meningitidis, Streptococcus pneumoniae, Listeria monocytogenes, Haemophilus influenzae and Escherichia coli. Here, we describe BMScan (Bacterial Meningitis Scan), a whole-genome analysis tool for the species identification of bacterial meningitis-causing and closely-related pathogens, an essential step for case management and disease surveillance. BMScan relies on a reference collection that contains genomes for 17 focal species to scan against to identify a given species. We established this reference collection by supplementing publically available genomes from RefSeq with genomes from the isolate collections of the Centers for Disease Control Bacterial Meningitis Laboratory and the Minnesota Department of Health Public Health Laboratory, and then filtered them down to a representative set of genomes which capture the diversity for each species. Using this reference collection, we evaluated two genomic comparison algorithms, Mash and Average Nucleotide Identity, for their ability to accurately and rapidly identify our focal species. RESULTS: We found that the results of Mash were strongly correlated with the results of ANI for species identification, while providing a significant reduction in run-time. This drastic difference in run-time enabled the rapid scanning of large reference genome collections, which, when combined with species-specific threshold values, facilitated the development of BMScan. Using a validation set of 15,503 genomes of our species of interest, BMScan accurately identified 99.97% of the species within 16 min 47 s. CONCLUSIONS: Identification of the bacterial meningitis pathogenic species is a critical step for case confirmation and further strain characterization. BMScan employs species-specific thresholds for previously-validated, genome-wide similarity statistics compiled from a curated reference genome collection to rapidly and accurately identify the species of uncharacterized bacterial meningitis pathogens and closely related pathogens. BMScan will facilitate the transition in public health laboratories from traditional phenotypic detection methods to whole genome sequencing based methods for species identification. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12879-018-3324-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-60944662018-08-20 BMScan: using whole genome similarity to rapidly and accurately identify bacterial meningitis causing species Topaz, Nadav Boxrud, Dave Retchless, Adam C. Nichols, Megan Chang, How-Yi Hu, Fang Wang, Xin BMC Infect Dis Software BACKGROUND: Bacterial meningitis is a life-threatening infection that remains a public health concern. Bacterial meningitis is commonly caused by the following species: Neisseria meningitidis, Streptococcus pneumoniae, Listeria monocytogenes, Haemophilus influenzae and Escherichia coli. Here, we describe BMScan (Bacterial Meningitis Scan), a whole-genome analysis tool for the species identification of bacterial meningitis-causing and closely-related pathogens, an essential step for case management and disease surveillance. BMScan relies on a reference collection that contains genomes for 17 focal species to scan against to identify a given species. We established this reference collection by supplementing publically available genomes from RefSeq with genomes from the isolate collections of the Centers for Disease Control Bacterial Meningitis Laboratory and the Minnesota Department of Health Public Health Laboratory, and then filtered them down to a representative set of genomes which capture the diversity for each species. Using this reference collection, we evaluated two genomic comparison algorithms, Mash and Average Nucleotide Identity, for their ability to accurately and rapidly identify our focal species. RESULTS: We found that the results of Mash were strongly correlated with the results of ANI for species identification, while providing a significant reduction in run-time. This drastic difference in run-time enabled the rapid scanning of large reference genome collections, which, when combined with species-specific threshold values, facilitated the development of BMScan. Using a validation set of 15,503 genomes of our species of interest, BMScan accurately identified 99.97% of the species within 16 min 47 s. CONCLUSIONS: Identification of the bacterial meningitis pathogenic species is a critical step for case confirmation and further strain characterization. BMScan employs species-specific thresholds for previously-validated, genome-wide similarity statistics compiled from a curated reference genome collection to rapidly and accurately identify the species of uncharacterized bacterial meningitis pathogens and closely related pathogens. BMScan will facilitate the transition in public health laboratories from traditional phenotypic detection methods to whole genome sequencing based methods for species identification. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12879-018-3324-1) contains supplementary material, which is available to authorized users. BioMed Central 2018-08-15 /pmc/articles/PMC6094466/ /pubmed/30111301 http://dx.doi.org/10.1186/s12879-018-3324-1 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Software
Topaz, Nadav
Boxrud, Dave
Retchless, Adam C.
Nichols, Megan
Chang, How-Yi
Hu, Fang
Wang, Xin
BMScan: using whole genome similarity to rapidly and accurately identify bacterial meningitis causing species
title BMScan: using whole genome similarity to rapidly and accurately identify bacterial meningitis causing species
title_full BMScan: using whole genome similarity to rapidly and accurately identify bacterial meningitis causing species
title_fullStr BMScan: using whole genome similarity to rapidly and accurately identify bacterial meningitis causing species
title_full_unstemmed BMScan: using whole genome similarity to rapidly and accurately identify bacterial meningitis causing species
title_short BMScan: using whole genome similarity to rapidly and accurately identify bacterial meningitis causing species
title_sort bmscan: using whole genome similarity to rapidly and accurately identify bacterial meningitis causing species
topic Software
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6094466/
https://www.ncbi.nlm.nih.gov/pubmed/30111301
http://dx.doi.org/10.1186/s12879-018-3324-1
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