Dissemination of IncQ1 Plasmids Harboring NTEKPC-IId in a Brazilian Hospital

KPC is a clinically significant serine carbapenemase in most countries, and its rapid spread threatens global public health. <i>bla</i><sub>KPC</sub> transmission is commonly mediated by Tn<i>4401</i> transposons. The <i>bla</i><sub>KPC</sub> gene has also been found in <i>non-Tn4401 elements</i> (NTE<sub>KPC</sub>). To fill the gap in the understanding of the stability and dissemination of NTE<sub>KPC</sub>-carrying plasmids, we selected and characterized carbapenem-resistant bacteria isolated between 2009 and 2016 from a hospital for a retrospective study of their plasmids conjugation capacity, impact on fitness, and replication in different species. Different clones were selected using PFGE, and their genomes were sequenced using Illumina and Oxford Nanopore methods. Minimum inhibitory concentrations (MICs) were determined by broth microdilution. Plasmid copy numbers (PCNs) were determined using qPCR. Doubling time was used to analyze fitness change. Most isolates (67%, 33/49) carried <i>bla</i><sub>KPC</sub>, of which 85% presented <i>bla</i><sub>KPC</sub> in a NTE<sub>KPC</sub>. The 25 isolates selected presented the <i>bla</i><sub>KPC</sub> gene in NTE<sub>KPC</sub>-IId in IncQ1-type plasmids, showing multispecies dissemination. IncQ1 plasmids were mobilizable and PCN seemed to be directly linked to the species, presenting a high-copy number, mainly in <i>K. pneumoniae</i>. No relationship was observed between IncQ1 PCN and carbapenems MIC values. IncQ1 and a conjugative plasmid from <i>K. pneumoniae</i> BHKPC10 were transferred to <i>E. coli</i> J53 without fitness changes, and MIC values were maintained for carbapenems despite the low transconjugant PCN. In addition to IncQ1 with NTE<sub>KPC</sub>, <i>Enterobacter cloacae</i> BHKPC28 contained the <i>mcr-9</i> gene in an IncHI2/IncHI2A conjugative plasmid, which may help the mobility of IncQ1 and the dissemination of two resistance determinants to last-resort antibiotics. Understanding the interaction between plasmids and high-risk lineages can help develop new therapies to prevent the dissemination of resistance traits.

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Journal
Microorganisms
Published
2025-01-16
DOI
https://doi.org/10.3390/microorganisms13010180
Citations
2
Primary Topic
Antibiotic Resistance in Bacteria
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article
Field-Weighted Citation Impact
1.18
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article

Dissemination of IncQ1 Plasmids Harboring NTEKPC-IId in a Brazilian Hospital

Edna Mariléa Meireles Leite, Rodrigo Meneses, Ilana Lopes Baratella da Cunha Camargo, Camila Maria dos Santos Boralli et al.
2 citations
Microorganisms
Antibiotic Resistance in Bacteria
1.18
article

Dissemination of IncQ1 Plasmids Harboring NTEKPC-IId in a Brazilian Hospital

Edna Mariléa Meireles Leite, Rodrigo Meneses, Ilana Lopes Baratella da Cunha Camargo, Camila Maria dos Santos Boralli, Julián Paganini, Fernanda L. Paganelli, Camila Pacheco Silveira Martins da Mata, Anita C. Schürch, Rob J. L. Willems
article en
2 citations

Abstract

KPC is a clinically significant serine carbapenemase in most countries, and its rapid spread threatens global public health. <i>bla</i><sub>KPC</sub> transmission is commonly mediated by Tn<i>4401</i> transposons. The <i>bla</i><sub>KPC</sub> gene has also been found in <i>non-Tn4401 elements</i> (NTE<sub>KPC</sub>). To fill the gap in the understanding of the stability and dissemination of NTE<sub>KPC</sub>-carrying plasmids, we selected and characterized carbapenem-resistant bacteria isolated between 2009 and 2016 from a hospital for a retrospective study of their plasmids conjugation capacity, impact on fitness, and replication in different species. Different clones were selected using PFGE, and their genomes were sequenced using Illumina and Oxford Nanopore methods. Minimum inhibitory concentrations (MICs) were determined by broth microdilution. Plasmid copy numbers (PCNs) were determined using qPCR. Doubling time was used to analyze fitness change. Most isolates (67%, 33/49) carried <i>bla</i><sub>KPC</sub>, of which 85% presented <i>bla</i><sub>KPC</sub> in a NTE<sub>KPC</sub>. The 25 isolates selected presented the <i>bla</i><sub>KPC</sub> gene in NTE<sub>KPC</sub>-IId in IncQ1-type plasmids, showing multispecies dissemination. IncQ1 plasmids were mobilizable and PCN seemed to be directly linked to the species, presenting a high-copy number, mainly in <i>K. pneumoniae</i>. No relationship was observed between IncQ1 PCN and carbapenems MIC values. IncQ1 and a conjugative plasmid from <i>K. pneumoniae</i> BHKPC10 were transferred to <i>E. coli</i> J53 without fitness changes, and MIC values were maintained for carbapenems despite the low transconjugant PCN. In addition to IncQ1 with NTE<sub>KPC</sub>, <i>Enterobacter cloacae</i> BHKPC28 contained the <i>mcr-9</i> gene in an IncHI2/IncHI2A conjugative plasmid, which may help the mobility of IncQ1 and the dissemination of two resistance determinants to last-resort antibiotics. Understanding the interaction between plasmids and high-risk lineages can help develop new therapies to prevent the dissemination of resistance traits.

MicroorganismsVol. 13(1)
Universidade Federal de São Carlos (BR), Universidade de São Paulo (BR), University Medical Center Utrecht (NL), Hospital Risoleta Tolentino Neves (BR)
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Openalex Percentile: Top 26%
Antibiotic Resistance in Bacteria
1.18
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