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First Detection and Molecular Characterization of Pseudomonas aeruginosa bla(NDM-1) ST308 in Greece
The objective of the present study is to report the detection and the molecular characterization of nine bla(NDM-1)-positive Pseudomonas aeruginosa isolates, all of which belonged to the epidemic high-risk international clone ST308, and all were isolated from patients in a tertiary care hospital in...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10537375/ https://www.ncbi.nlm.nih.gov/pubmed/37764003 http://dx.doi.org/10.3390/microorganisms11092159 |
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author | Tsilipounidaki, Katerina Gkountinoudis, Christos-George Florou, Zoi Fthenakis, George C. Miriagou, Vivi Petinaki, Efthymia |
author_facet | Tsilipounidaki, Katerina Gkountinoudis, Christos-George Florou, Zoi Fthenakis, George C. Miriagou, Vivi Petinaki, Efthymia |
author_sort | Tsilipounidaki, Katerina |
collection | PubMed |
description | The objective of the present study is to report the detection and the molecular characterization of nine bla(NDM-1)-positive Pseudomonas aeruginosa isolates, all of which belonged to the epidemic high-risk international clone ST308, and all were isolated from patients in a tertiary care hospital in Central Greece from May to July 2023.The isolates were characterized by whole genome sequencing to obtain multi-locus sequencing typing (MLST) and identify the bla(NDM1)-environment and resistome and virulence genes content. In silico MLST analysis showed that all isolates belonged to the high-risk ST308 international clone. All strains possessed 22 different genes, encoding resistance to various antimicrobial agents. Whole genome sequencing revealed that the bla(NDM-1) was chromosomally located within the integrative and conjugative element ICE(Tn4371)6385 and that it was part of one cassette along with two other resistance genes, floR and msrE. Two additional resistance cassettes were also found in the genome, which included the arrays of aph(6)-Id, aph(3″)-Ib, floR, sul2 and aadA10, qnrVC1, aac(3)-Id, dfrB5, aac(6′)-II. Additionally, the strains possessed various virulence genes, e.g., aprA, exoU, lasA, lasB, toxA, and estA. All of the isolates shared identical genomes, which showed 98% similarity with the P. aeruginosa ST308 genome (acc. no CP020703), previously reported from Singapore. To our knowledge, this is the first report of ST308 bla(NDM-1)-positive P. aeruginosa isolation in Europe, which indicates the transmission dynamics of this high-risk clone. |
format | Online Article Text |
id | pubmed-10537375 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-105373752023-09-29 First Detection and Molecular Characterization of Pseudomonas aeruginosa bla(NDM-1) ST308 in Greece Tsilipounidaki, Katerina Gkountinoudis, Christos-George Florou, Zoi Fthenakis, George C. Miriagou, Vivi Petinaki, Efthymia Microorganisms Communication The objective of the present study is to report the detection and the molecular characterization of nine bla(NDM-1)-positive Pseudomonas aeruginosa isolates, all of which belonged to the epidemic high-risk international clone ST308, and all were isolated from patients in a tertiary care hospital in Central Greece from May to July 2023.The isolates were characterized by whole genome sequencing to obtain multi-locus sequencing typing (MLST) and identify the bla(NDM1)-environment and resistome and virulence genes content. In silico MLST analysis showed that all isolates belonged to the high-risk ST308 international clone. All strains possessed 22 different genes, encoding resistance to various antimicrobial agents. Whole genome sequencing revealed that the bla(NDM-1) was chromosomally located within the integrative and conjugative element ICE(Tn4371)6385 and that it was part of one cassette along with two other resistance genes, floR and msrE. Two additional resistance cassettes were also found in the genome, which included the arrays of aph(6)-Id, aph(3″)-Ib, floR, sul2 and aadA10, qnrVC1, aac(3)-Id, dfrB5, aac(6′)-II. Additionally, the strains possessed various virulence genes, e.g., aprA, exoU, lasA, lasB, toxA, and estA. All of the isolates shared identical genomes, which showed 98% similarity with the P. aeruginosa ST308 genome (acc. no CP020703), previously reported from Singapore. To our knowledge, this is the first report of ST308 bla(NDM-1)-positive P. aeruginosa isolation in Europe, which indicates the transmission dynamics of this high-risk clone. MDPI 2023-08-26 /pmc/articles/PMC10537375/ /pubmed/37764003 http://dx.doi.org/10.3390/microorganisms11092159 Text en © 2023 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 | Communication Tsilipounidaki, Katerina Gkountinoudis, Christos-George Florou, Zoi Fthenakis, George C. Miriagou, Vivi Petinaki, Efthymia First Detection and Molecular Characterization of Pseudomonas aeruginosa bla(NDM-1) ST308 in Greece |
title | First Detection and Molecular Characterization of Pseudomonas aeruginosa bla(NDM-1) ST308 in Greece |
title_full | First Detection and Molecular Characterization of Pseudomonas aeruginosa bla(NDM-1) ST308 in Greece |
title_fullStr | First Detection and Molecular Characterization of Pseudomonas aeruginosa bla(NDM-1) ST308 in Greece |
title_full_unstemmed | First Detection and Molecular Characterization of Pseudomonas aeruginosa bla(NDM-1) ST308 in Greece |
title_short | First Detection and Molecular Characterization of Pseudomonas aeruginosa bla(NDM-1) ST308 in Greece |
title_sort | first detection and molecular characterization of pseudomonas aeruginosa bla(ndm-1) st308 in greece |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10537375/ https://www.ncbi.nlm.nih.gov/pubmed/37764003 http://dx.doi.org/10.3390/microorganisms11092159 |
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