Genomic Insight of VIM-harboring IncA Plasmid from a Clinical ST69 <i>Escherichia coli</i> Strain in Italy
<i>Background</i>: VIM (Verona Integron-encoded Metallo-beta-lactamase) is a member of the Metallo-Beta-Lactamases (MBLs), and is able to hydrolyze all beta-lactams antibiotics, except for monobactams, and including carbapenems. Here we characterize a VIM-producing IncA plasmid isolated...
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doaj-ab03ba6be99c4a4986d5bdbad7af6b022020-11-25T03:13:33ZengMDPI AGMicroorganisms2076-26072020-08-0181232123210.3390/microorganisms8081232Genomic Insight of VIM-harboring IncA Plasmid from a Clinical ST69 <i>Escherichia coli</i> Strain in ItalyVittoria Mattioni Marchetti0Ibrahim Bitar1Aurora Piazza2Alessandra Mercato3Elena Fogato4Jaroslav Hrabak5Roberta Migliavacca6Department of Microbiology, Faculty of Medicine, University Hospital in Pilsen, Charles University, 32300 Pilsen, Czech RepublicDepartment of Microbiology, Faculty of Medicine, University Hospital in Pilsen, Charles University, 32300 Pilsen, Czech RepublicDepartment of Clinical-Surgical, Diagnostic and Pediatric Sciences, Unit of Microbiology and Clinical Microbiology, University of Pavia, 27100 Pavia, ItalyDepartment of Clinical-Surgical, Diagnostic and Pediatric Sciences, Unit of Microbiology and Clinical Microbiology, University of Pavia, 27100 Pavia, ItalyClinical Microbiology Laboratory, ASP Golgi-Redaelli Hospital, Via Olmetto, 20123 Milan, ItalyDepartment of Microbiology, Faculty of Medicine, University Hospital in Pilsen, Charles University, 32300 Pilsen, Czech RepublicDepartment of Clinical-Surgical, Diagnostic and Pediatric Sciences, Unit of Microbiology and Clinical Microbiology, University of Pavia, 27100 Pavia, Italy<i>Background</i>: VIM (Verona Integron-encoded Metallo-beta-lactamase) is a member of the Metallo-Beta-Lactamases (MBLs), and is able to hydrolyze all beta-lactams antibiotics, except for monobactams, and including carbapenems. Here we characterize a VIM-producing IncA plasmid isolated from a clinical ST69 <i>Escherichia coli</i> strain from an Italian Long-Term Care Facility (LTCF) inpatient. <i>Methods</i>: An antimicrobial susceptibility test and conjugation assay were carried out, and the transferability of the <i>bla</i><sub>VIM-type </sub>gene was confirmed in the transconjugant. Whole-genome sequencing (WGS) of the strain 550 was performed using the Sequel I platform. Genome assembly was performed using “Microbial Assembly”. Genomic analysis was conducted by uploading the contigs to ResFinder and PlasmidFinder databases. <i>Results: </i>Assembly resulted in three complete circular contigs: the chromosome (4,962,700 bp), an IncA plasmid (p550_IncA_VIM_1; 162,608 bp), harboring genes coding for aminoglycoside resistance (<i>aac(6′)-Ib4</i>, <i>ant(3″)-Ia</i>, <i>aph(3″)-Ib</i>, <i>aph(3′)-XV</i>, <i>aph(6)-Id</i>), beta-lactam resistance (<i>bla</i><sub>SHV-12</sub>, <i>bla</i><sub>VIM-1</sub>), macrolides resistance (<i>mph(A)</i>), phenicol resistance (<i>catB2</i>), quinolones resistance (<i>qnrS1</i>), sulphonamide resistance (<i>sul1</i>, <i>sul2</i>), and trimethoprim resistance (<i>dfrA14</i>), and an IncK/Z plasmid (p550_IncB_O_K_Z; 100,306 bp), free of antibiotic resistance genes. <i>Conclusions:</i> The increase in reports of IncA plasmids bearing different antimicrobial resistance genes highlights the overall important role of IncA plasmids in disseminating carbapenemase genes, with a preference for the <i>bla</i><sub>VIM-1 </sub>gene in Italy.https://www.mdpi.com/2076-2607/8/8/1232<i>E. coli</i><i>bla</i>VIM-1<i>IncA</i> |
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DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Vittoria Mattioni Marchetti Ibrahim Bitar Aurora Piazza Alessandra Mercato Elena Fogato Jaroslav Hrabak Roberta Migliavacca |
spellingShingle |
Vittoria Mattioni Marchetti Ibrahim Bitar Aurora Piazza Alessandra Mercato Elena Fogato Jaroslav Hrabak Roberta Migliavacca Genomic Insight of VIM-harboring IncA Plasmid from a Clinical ST69 <i>Escherichia coli</i> Strain in Italy Microorganisms <i>E. coli</i> <i>bla</i>VIM-1 <i>IncA</i> |
author_facet |
Vittoria Mattioni Marchetti Ibrahim Bitar Aurora Piazza Alessandra Mercato Elena Fogato Jaroslav Hrabak Roberta Migliavacca |
author_sort |
Vittoria Mattioni Marchetti |
title |
Genomic Insight of VIM-harboring IncA Plasmid from a Clinical ST69 <i>Escherichia coli</i> Strain in Italy |
title_short |
Genomic Insight of VIM-harboring IncA Plasmid from a Clinical ST69 <i>Escherichia coli</i> Strain in Italy |
title_full |
Genomic Insight of VIM-harboring IncA Plasmid from a Clinical ST69 <i>Escherichia coli</i> Strain in Italy |
title_fullStr |
Genomic Insight of VIM-harboring IncA Plasmid from a Clinical ST69 <i>Escherichia coli</i> Strain in Italy |
title_full_unstemmed |
Genomic Insight of VIM-harboring IncA Plasmid from a Clinical ST69 <i>Escherichia coli</i> Strain in Italy |
title_sort |
genomic insight of vim-harboring inca plasmid from a clinical st69 <i>escherichia coli</i> strain in italy |
publisher |
MDPI AG |
series |
Microorganisms |
issn |
2076-2607 |
publishDate |
2020-08-01 |
description |
<i>Background</i>: VIM (Verona Integron-encoded Metallo-beta-lactamase) is a member of the Metallo-Beta-Lactamases (MBLs), and is able to hydrolyze all beta-lactams antibiotics, except for monobactams, and including carbapenems. Here we characterize a VIM-producing IncA plasmid isolated from a clinical ST69 <i>Escherichia coli</i> strain from an Italian Long-Term Care Facility (LTCF) inpatient. <i>Methods</i>: An antimicrobial susceptibility test and conjugation assay were carried out, and the transferability of the <i>bla</i><sub>VIM-type </sub>gene was confirmed in the transconjugant. Whole-genome sequencing (WGS) of the strain 550 was performed using the Sequel I platform. Genome assembly was performed using “Microbial Assembly”. Genomic analysis was conducted by uploading the contigs to ResFinder and PlasmidFinder databases. <i>Results: </i>Assembly resulted in three complete circular contigs: the chromosome (4,962,700 bp), an IncA plasmid (p550_IncA_VIM_1; 162,608 bp), harboring genes coding for aminoglycoside resistance (<i>aac(6′)-Ib4</i>, <i>ant(3″)-Ia</i>, <i>aph(3″)-Ib</i>, <i>aph(3′)-XV</i>, <i>aph(6)-Id</i>), beta-lactam resistance (<i>bla</i><sub>SHV-12</sub>, <i>bla</i><sub>VIM-1</sub>), macrolides resistance (<i>mph(A)</i>), phenicol resistance (<i>catB2</i>), quinolones resistance (<i>qnrS1</i>), sulphonamide resistance (<i>sul1</i>, <i>sul2</i>), and trimethoprim resistance (<i>dfrA14</i>), and an IncK/Z plasmid (p550_IncB_O_K_Z; 100,306 bp), free of antibiotic resistance genes. <i>Conclusions:</i> The increase in reports of IncA plasmids bearing different antimicrobial resistance genes highlights the overall important role of IncA plasmids in disseminating carbapenemase genes, with a preference for the <i>bla</i><sub>VIM-1 </sub>gene in Italy. |
topic |
<i>E. coli</i> <i>bla</i>VIM-1 <i>IncA</i> |
url |
https://www.mdpi.com/2076-2607/8/8/1232 |
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