Cargando…

Comparative Genomics of Nonoutbreak Pseudomonas aeruginosa Strains Underlines Genome Plasticity and Geographic Relatedness of the Global Clone ST235

Pseudomonas aeruginosa is an important opportunistic pathogen in hospitals, responsible for various infections that are difficult to treat due to intrinsic and acquired antibiotic resistance. Here, 20 epidemiologically unrelated strains isolated from patients in a general hospital over a time period...

Descripción completa

Detalles Bibliográficos
Autores principales: Brüggemann, Holger, Migliorini, Leticia Busato, de Sales, Romario Oliveira, Koga, Paula Célia Mariko, de Souza, Andrea Vieira, Jensen, Anders, Poehlein, Anja, Brzuszkiewicz, Elzbieta, Doi, Andre Mario, Pasternak, Jacyr, Martino, Marines Dalla Valle, Severino, Patricia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6063271/
https://www.ncbi.nlm.nih.gov/pubmed/29982603
http://dx.doi.org/10.1093/gbe/evy139
_version_ 1783342525241622528
author Brüggemann, Holger
Migliorini, Leticia Busato
de Sales, Romario Oliveira
Koga, Paula Célia Mariko
de Souza, Andrea Vieira
Jensen, Anders
Poehlein, Anja
Brzuszkiewicz, Elzbieta
Doi, Andre Mario
Pasternak, Jacyr
Martino, Marines Dalla Valle
Severino, Patricia
author_facet Brüggemann, Holger
Migliorini, Leticia Busato
de Sales, Romario Oliveira
Koga, Paula Célia Mariko
de Souza, Andrea Vieira
Jensen, Anders
Poehlein, Anja
Brzuszkiewicz, Elzbieta
Doi, Andre Mario
Pasternak, Jacyr
Martino, Marines Dalla Valle
Severino, Patricia
author_sort Brüggemann, Holger
collection PubMed
description Pseudomonas aeruginosa is an important opportunistic pathogen in hospitals, responsible for various infections that are difficult to treat due to intrinsic and acquired antibiotic resistance. Here, 20 epidemiologically unrelated strains isolated from patients in a general hospital over a time period of two decades were analyzed using whole genome sequencing. The genomes were compared in order to assess the presence of a predominant clone or sequence type (ST). No clonal structure was identified, but core genome-based single nucleotide polymorphism (SNP) analysis distinguished two major, previously identified phylogenetic groups. Interestingly, most of the older strains isolated between 1994 and 1998 harbored exoU, encoding a cytotoxic phospholipase. In contrast, most strains isolated between 2011 and 2016 were exoU-negative and phylogenetically very distinct from the older strains, suggesting a population shift of nosocomial P. aeruginosa over time. Three out of 20 strains were ST235 strains, a global high-risk clonal lineage; these carried several additional resistance determinants including aac(6’)Ib-cr encoding an aminoglycoside N-acetyltransferase that confers resistance to fluoroquinolones. Core genome comparison with ST235 strains from other parts of the world showed that the three strains clustered together with other Brazilian/Argentinean isolates. Despite this regional relatedness, the individuality of each of the three ST235 strains was revealed by core genome-based SNPs and the presence of genomic islands in the accessory genome. Similarly, strain-specific characteristics were detected for the remaining strains, indicative of individual evolutionary histories and elevated genome plasticity.
format Online
Article
Text
id pubmed-6063271
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-60632712018-08-09 Comparative Genomics of Nonoutbreak Pseudomonas aeruginosa Strains Underlines Genome Plasticity and Geographic Relatedness of the Global Clone ST235 Brüggemann, Holger Migliorini, Leticia Busato de Sales, Romario Oliveira Koga, Paula Célia Mariko de Souza, Andrea Vieira Jensen, Anders Poehlein, Anja Brzuszkiewicz, Elzbieta Doi, Andre Mario Pasternak, Jacyr Martino, Marines Dalla Valle Severino, Patricia Genome Biol Evol Genome Report Pseudomonas aeruginosa is an important opportunistic pathogen in hospitals, responsible for various infections that are difficult to treat due to intrinsic and acquired antibiotic resistance. Here, 20 epidemiologically unrelated strains isolated from patients in a general hospital over a time period of two decades were analyzed using whole genome sequencing. The genomes were compared in order to assess the presence of a predominant clone or sequence type (ST). No clonal structure was identified, but core genome-based single nucleotide polymorphism (SNP) analysis distinguished two major, previously identified phylogenetic groups. Interestingly, most of the older strains isolated between 1994 and 1998 harbored exoU, encoding a cytotoxic phospholipase. In contrast, most strains isolated between 2011 and 2016 were exoU-negative and phylogenetically very distinct from the older strains, suggesting a population shift of nosocomial P. aeruginosa over time. Three out of 20 strains were ST235 strains, a global high-risk clonal lineage; these carried several additional resistance determinants including aac(6’)Ib-cr encoding an aminoglycoside N-acetyltransferase that confers resistance to fluoroquinolones. Core genome comparison with ST235 strains from other parts of the world showed that the three strains clustered together with other Brazilian/Argentinean isolates. Despite this regional relatedness, the individuality of each of the three ST235 strains was revealed by core genome-based SNPs and the presence of genomic islands in the accessory genome. Similarly, strain-specific characteristics were detected for the remaining strains, indicative of individual evolutionary histories and elevated genome plasticity. Oxford University Press 2018-07-03 /pmc/articles/PMC6063271/ /pubmed/29982603 http://dx.doi.org/10.1093/gbe/evy139 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://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 Genome Report
Brüggemann, Holger
Migliorini, Leticia Busato
de Sales, Romario Oliveira
Koga, Paula Célia Mariko
de Souza, Andrea Vieira
Jensen, Anders
Poehlein, Anja
Brzuszkiewicz, Elzbieta
Doi, Andre Mario
Pasternak, Jacyr
Martino, Marines Dalla Valle
Severino, Patricia
Comparative Genomics of Nonoutbreak Pseudomonas aeruginosa Strains Underlines Genome Plasticity and Geographic Relatedness of the Global Clone ST235
title Comparative Genomics of Nonoutbreak Pseudomonas aeruginosa Strains Underlines Genome Plasticity and Geographic Relatedness of the Global Clone ST235
title_full Comparative Genomics of Nonoutbreak Pseudomonas aeruginosa Strains Underlines Genome Plasticity and Geographic Relatedness of the Global Clone ST235
title_fullStr Comparative Genomics of Nonoutbreak Pseudomonas aeruginosa Strains Underlines Genome Plasticity and Geographic Relatedness of the Global Clone ST235
title_full_unstemmed Comparative Genomics of Nonoutbreak Pseudomonas aeruginosa Strains Underlines Genome Plasticity and Geographic Relatedness of the Global Clone ST235
title_short Comparative Genomics of Nonoutbreak Pseudomonas aeruginosa Strains Underlines Genome Plasticity and Geographic Relatedness of the Global Clone ST235
title_sort comparative genomics of nonoutbreak pseudomonas aeruginosa strains underlines genome plasticity and geographic relatedness of the global clone st235
topic Genome Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6063271/
https://www.ncbi.nlm.nih.gov/pubmed/29982603
http://dx.doi.org/10.1093/gbe/evy139
work_keys_str_mv AT bruggemannholger comparativegenomicsofnonoutbreakpseudomonasaeruginosastrainsunderlinesgenomeplasticityandgeographicrelatednessoftheglobalclonest235
AT migliorinileticiabusato comparativegenomicsofnonoutbreakpseudomonasaeruginosastrainsunderlinesgenomeplasticityandgeographicrelatednessoftheglobalclonest235
AT desalesromariooliveira comparativegenomicsofnonoutbreakpseudomonasaeruginosastrainsunderlinesgenomeplasticityandgeographicrelatednessoftheglobalclonest235
AT kogapaulaceliamariko comparativegenomicsofnonoutbreakpseudomonasaeruginosastrainsunderlinesgenomeplasticityandgeographicrelatednessoftheglobalclonest235
AT desouzaandreavieira comparativegenomicsofnonoutbreakpseudomonasaeruginosastrainsunderlinesgenomeplasticityandgeographicrelatednessoftheglobalclonest235
AT jensenanders comparativegenomicsofnonoutbreakpseudomonasaeruginosastrainsunderlinesgenomeplasticityandgeographicrelatednessoftheglobalclonest235
AT poehleinanja comparativegenomicsofnonoutbreakpseudomonasaeruginosastrainsunderlinesgenomeplasticityandgeographicrelatednessoftheglobalclonest235
AT brzuszkiewiczelzbieta comparativegenomicsofnonoutbreakpseudomonasaeruginosastrainsunderlinesgenomeplasticityandgeographicrelatednessoftheglobalclonest235
AT doiandremario comparativegenomicsofnonoutbreakpseudomonasaeruginosastrainsunderlinesgenomeplasticityandgeographicrelatednessoftheglobalclonest235
AT pasternakjacyr comparativegenomicsofnonoutbreakpseudomonasaeruginosastrainsunderlinesgenomeplasticityandgeographicrelatednessoftheglobalclonest235
AT martinomarinesdallavalle comparativegenomicsofnonoutbreakpseudomonasaeruginosastrainsunderlinesgenomeplasticityandgeographicrelatednessoftheglobalclonest235
AT severinopatricia comparativegenomicsofnonoutbreakpseudomonasaeruginosastrainsunderlinesgenomeplasticityandgeographicrelatednessoftheglobalclonest235