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A Core Genome Multilocus Sequence Typing Scheme for Pseudomonas aeruginosa
Pseudomonas aeruginosa is a ubiquitous microorganism and an important opportunistic pathogen responsible for a broad spectrum of infections mainly in immunosuppressed and critically ill patients. Molecular investigations traditionally rely on pulsed field gel electrophoresis (PFGE) and multilocus se...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7264379/ https://www.ncbi.nlm.nih.gov/pubmed/32528447 http://dx.doi.org/10.3389/fmicb.2020.01049 |
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author | de Sales, Romário Oliveira Migliorini, Letícia Busato Puga, Renato Kocsis, Bela Severino, Patricia |
author_facet | de Sales, Romário Oliveira Migliorini, Letícia Busato Puga, Renato Kocsis, Bela Severino, Patricia |
author_sort | de Sales, Romário Oliveira |
collection | PubMed |
description | Pseudomonas aeruginosa is a ubiquitous microorganism and an important opportunistic pathogen responsible for a broad spectrum of infections mainly in immunosuppressed and critically ill patients. Molecular investigations traditionally rely on pulsed field gel electrophoresis (PFGE) and multilocus sequence typing (MLST). In this work we propose a core genome multilocus sequence typing (cgMLST) scheme for P. aeruginosa, a methodology that combines traditional MLST principles with whole genome sequencing data. All publicly available complete P. aeruginosa genomes, representing the diversity of this species, were used to establish a cgMLST scheme targeting 2,653 genes. The scheme was then tested using genomes available at contig, chromosome and scaffold levels. The proposed cgMLST scheme for P. aeruginosa typed over 99% (2,314/2,325) of the genomes available for this study considering at least 95% of the cgMLST target genes present. The absence of a certain number gene targets at the threshold considered for both the creation and validation steps due to low genome sequence quality is possibly the main reason for this result. The cgMLST scheme was compared with previously published whole genome single nucleotide polymorphism analysis for the characterization of the population structure of the epidemic clone ST235 and results were highly similar. In order to evaluate the typing resolution of the proposed scheme, collections of isolates belonging to two important STs associated with cystic fibrosis, ST146 and ST274, were typed using this scheme, and ST235 isolates associated with an outbreak were evaluated. Besides confirming the relatedness of all the isolates, earlier determined by MLST, the higher resolution of cgMLST denotes that it may be suitable for surveillance programs, overcoming possible shortcomings of classical MLST. The proposed scheme is publicly available at: https://github.com/BioinformaticsHIAEMolecularMicrobiology/cgMLST-Pseudomonas-aeruginosa. |
format | Online Article Text |
id | pubmed-7264379 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72643792020-06-10 A Core Genome Multilocus Sequence Typing Scheme for Pseudomonas aeruginosa de Sales, Romário Oliveira Migliorini, Letícia Busato Puga, Renato Kocsis, Bela Severino, Patricia Front Microbiol Microbiology Pseudomonas aeruginosa is a ubiquitous microorganism and an important opportunistic pathogen responsible for a broad spectrum of infections mainly in immunosuppressed and critically ill patients. Molecular investigations traditionally rely on pulsed field gel electrophoresis (PFGE) and multilocus sequence typing (MLST). In this work we propose a core genome multilocus sequence typing (cgMLST) scheme for P. aeruginosa, a methodology that combines traditional MLST principles with whole genome sequencing data. All publicly available complete P. aeruginosa genomes, representing the diversity of this species, were used to establish a cgMLST scheme targeting 2,653 genes. The scheme was then tested using genomes available at contig, chromosome and scaffold levels. The proposed cgMLST scheme for P. aeruginosa typed over 99% (2,314/2,325) of the genomes available for this study considering at least 95% of the cgMLST target genes present. The absence of a certain number gene targets at the threshold considered for both the creation and validation steps due to low genome sequence quality is possibly the main reason for this result. The cgMLST scheme was compared with previously published whole genome single nucleotide polymorphism analysis for the characterization of the population structure of the epidemic clone ST235 and results were highly similar. In order to evaluate the typing resolution of the proposed scheme, collections of isolates belonging to two important STs associated with cystic fibrosis, ST146 and ST274, were typed using this scheme, and ST235 isolates associated with an outbreak were evaluated. Besides confirming the relatedness of all the isolates, earlier determined by MLST, the higher resolution of cgMLST denotes that it may be suitable for surveillance programs, overcoming possible shortcomings of classical MLST. The proposed scheme is publicly available at: https://github.com/BioinformaticsHIAEMolecularMicrobiology/cgMLST-Pseudomonas-aeruginosa. Frontiers Media S.A. 2020-05-26 /pmc/articles/PMC7264379/ /pubmed/32528447 http://dx.doi.org/10.3389/fmicb.2020.01049 Text en Copyright © 2020 de Sales, Migliorini, Puga, Kocsis and Severino. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology de Sales, Romário Oliveira Migliorini, Letícia Busato Puga, Renato Kocsis, Bela Severino, Patricia A Core Genome Multilocus Sequence Typing Scheme for Pseudomonas aeruginosa |
title | A Core Genome Multilocus Sequence Typing Scheme for Pseudomonas aeruginosa |
title_full | A Core Genome Multilocus Sequence Typing Scheme for Pseudomonas aeruginosa |
title_fullStr | A Core Genome Multilocus Sequence Typing Scheme for Pseudomonas aeruginosa |
title_full_unstemmed | A Core Genome Multilocus Sequence Typing Scheme for Pseudomonas aeruginosa |
title_short | A Core Genome Multilocus Sequence Typing Scheme for Pseudomonas aeruginosa |
title_sort | core genome multilocus sequence typing scheme for pseudomonas aeruginosa |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7264379/ https://www.ncbi.nlm.nih.gov/pubmed/32528447 http://dx.doi.org/10.3389/fmicb.2020.01049 |
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