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Complete Genome and Plasmids Sequences of a Clinical Proteus mirabilis Isolate Producing Plasmid Mediated NDM-1 From Italy
Background: The spread of carbapenemase genes, such as bla(NDM-1), in Proteus mirabilis poses a public health threat. The aim of the study was to characterize the genome and plasmids sequences of an NDM-1-positive strain (IBCRE14), which was isolated in 2019 from a catheterized patient hospitalized...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7142865/ https://www.ncbi.nlm.nih.gov/pubmed/32121207 http://dx.doi.org/10.3390/microorganisms8030339 |
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author | Bitar, Ibrahim Mattioni Marchetti, Vittoria Mercato, Alessandra Nucleo, Elisabetta Anesi, Adriano Bracco, Silvia Rognoni, Vanina Hrabak, Jaroslav Migliavacca, Roberta |
author_facet | Bitar, Ibrahim Mattioni Marchetti, Vittoria Mercato, Alessandra Nucleo, Elisabetta Anesi, Adriano Bracco, Silvia Rognoni, Vanina Hrabak, Jaroslav Migliavacca, Roberta |
author_sort | Bitar, Ibrahim |
collection | PubMed |
description | Background: The spread of carbapenemase genes, such as bla(NDM-1), in Proteus mirabilis poses a public health threat. The aim of the study was to characterize the genome and plasmids sequences of an NDM-1-positive strain (IBCRE14), which was isolated in 2019 from a catheterized patient hospitalized in Italy. Methods: Whole genome sequencing (WGS) of IBCRE14 was performed on extracted genomic DNA using Sequel I platform. Genome assembly was performed using “Microbial Assembly”. Genomic analysis was conducted by uploading the contigs to ResFinder and PlasmidFinder databases from the Center for Genomic Epidemiology. Results: IBCRE14 had a genome size of 4,018,329 bp and harboured genes coding for resistance to aminoglycosides (aadA1), phenicol (cat), tetracycline (tetJ), and trimethoprim (dfrA1). A large plasmid (pIB_NDM_1) harboured antibiotic resistance genes against sulphonamide (sul1), trimethoprim (dfrA14), tetracycline (tetB), rifampicin (arr-2), aminoglycosides (aadA1, aph3-VI), and beta-lactams (bla(OXA-10), bla(NDM-1)). Furthermore, a small plasmid (pIB_COL3M) harboured a qnrD1 gene coding for quinolone resistance. Conclusion: The ability to conjugate and the presence of a composite antibiotic resistance island suggests that pIB_NDM_1 could both acquire more resistance genes and easily disseminate. To our knowledge, this is the first report on an untypable plasmid harbouring bla(NDM-1) in P. mirabilis, in Italy. |
format | Online Article Text |
id | pubmed-7142865 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-71428652020-04-14 Complete Genome and Plasmids Sequences of a Clinical Proteus mirabilis Isolate Producing Plasmid Mediated NDM-1 From Italy Bitar, Ibrahim Mattioni Marchetti, Vittoria Mercato, Alessandra Nucleo, Elisabetta Anesi, Adriano Bracco, Silvia Rognoni, Vanina Hrabak, Jaroslav Migliavacca, Roberta Microorganisms Communication Background: The spread of carbapenemase genes, such as bla(NDM-1), in Proteus mirabilis poses a public health threat. The aim of the study was to characterize the genome and plasmids sequences of an NDM-1-positive strain (IBCRE14), which was isolated in 2019 from a catheterized patient hospitalized in Italy. Methods: Whole genome sequencing (WGS) of IBCRE14 was performed on extracted genomic DNA using Sequel I platform. Genome assembly was performed using “Microbial Assembly”. Genomic analysis was conducted by uploading the contigs to ResFinder and PlasmidFinder databases from the Center for Genomic Epidemiology. Results: IBCRE14 had a genome size of 4,018,329 bp and harboured genes coding for resistance to aminoglycosides (aadA1), phenicol (cat), tetracycline (tetJ), and trimethoprim (dfrA1). A large plasmid (pIB_NDM_1) harboured antibiotic resistance genes against sulphonamide (sul1), trimethoprim (dfrA14), tetracycline (tetB), rifampicin (arr-2), aminoglycosides (aadA1, aph3-VI), and beta-lactams (bla(OXA-10), bla(NDM-1)). Furthermore, a small plasmid (pIB_COL3M) harboured a qnrD1 gene coding for quinolone resistance. Conclusion: The ability to conjugate and the presence of a composite antibiotic resistance island suggests that pIB_NDM_1 could both acquire more resistance genes and easily disseminate. To our knowledge, this is the first report on an untypable plasmid harbouring bla(NDM-1) in P. mirabilis, in Italy. MDPI 2020-02-28 /pmc/articles/PMC7142865/ /pubmed/32121207 http://dx.doi.org/10.3390/microorganisms8030339 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Bitar, Ibrahim Mattioni Marchetti, Vittoria Mercato, Alessandra Nucleo, Elisabetta Anesi, Adriano Bracco, Silvia Rognoni, Vanina Hrabak, Jaroslav Migliavacca, Roberta Complete Genome and Plasmids Sequences of a Clinical Proteus mirabilis Isolate Producing Plasmid Mediated NDM-1 From Italy |
title | Complete Genome and Plasmids Sequences of a Clinical Proteus mirabilis Isolate Producing Plasmid Mediated NDM-1 From Italy |
title_full | Complete Genome and Plasmids Sequences of a Clinical Proteus mirabilis Isolate Producing Plasmid Mediated NDM-1 From Italy |
title_fullStr | Complete Genome and Plasmids Sequences of a Clinical Proteus mirabilis Isolate Producing Plasmid Mediated NDM-1 From Italy |
title_full_unstemmed | Complete Genome and Plasmids Sequences of a Clinical Proteus mirabilis Isolate Producing Plasmid Mediated NDM-1 From Italy |
title_short | Complete Genome and Plasmids Sequences of a Clinical Proteus mirabilis Isolate Producing Plasmid Mediated NDM-1 From Italy |
title_sort | complete genome and plasmids sequences of a clinical proteus mirabilis isolate producing plasmid mediated ndm-1 from italy |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7142865/ https://www.ncbi.nlm.nih.gov/pubmed/32121207 http://dx.doi.org/10.3390/microorganisms8030339 |
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