2019•Microbial Drug ResistanceRequires access

Increased Resistance to Carbapenems in Proteus mirabilis Mediated by Amplification of the bla VIM-1 -Carrying and IS 26 -Associated Class 1 Integron

Séverine Bontron, Laurent Poirel, Nicolas Kieffer, Encho Savov, Angelina Trifonova, Ива Тодорова, Gwendoline Kueffer, Patrice Nordmann

Open publisher page 27 citations

Abstract

Objective: The aim of the study was to decipher the mechanisms and associated genetic determinants responsible for increased carbapenem resistance among Proteus mirabilis clinical isolates. Methods: The entire genetic structure surrounding the β-lactam resistance genes was characterized by PCR, gene walking, and DNA sequencing. Results: A series of clinical P. mirabilis isolates were consecutively recovered from different patients at the Military hospital of Sofia, Bulgaria. They showed variable levels of resistance to carbapenems. All isolates produced the same carbapenemase VIM-1 that was chromosomally encoded. We showed that increased resistance to carbapenems was related to an increased number of bla VIM-1 gene copies. Conclusion: We showed here that increased carbapenem resistance in P. mirabilis may result from increased expression of the bla VIM-1 carbapenemase gene through multiplication of its copy number.

About this research paper

What this paper is about

Objective: The aim of the study was to decipher the mechanisms and associated genetic determinants responsible for increased carbapenem resistance among Proteus mirabilis clinical isolates. Methods: The entire genetic structure surrounding the β-lactam resistance genes was characterized by PCR, gene walking, and DNA sequencing. Results: A series of clinical P. mirabilis isolates were consecutively recovered from different patients at the Military hospital of Sofia, Bulgaria. They showed variable levels of resistance to carbapenems. All isolates produced the same carbapenemase VIM-1 that was chromosomally encoded. We showed that increased resistance to carbapenems was related to an increased number of bla VIM-1 gene copies. Conclusion: We showed here that increased carbapenem resistance in P. mirabilis may result from increased expression of the bla VIM-1 carbapenemase gene through multiplication of its copy number.

Why it matters

OpenAlex reports 27 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Objective: The aim of the study was to decipher the mechanisms and associated genetic determinants responsible for increased carbapenem resistance among Proteus mirabilis clinical isolates. Methods: The entire genetic structure surrounding the β-lactam resistance genes was characterized by PCR, gene walking, and DNA sequencing. Results: A series of clinical P. mirabilis isolates were consecutively recovered from different patients at the Military hospital of Sofia, Bulgaria. They showed variable levels of resistance to carbapenems. All isolates produced the same carbapenemase VIM-1 that was chromosomally encoded. We showed that increased resistance to carbapenems was related to an increased number of bla VIM-1 gene copies. Conclusion: We showed here that increased carbapenem resistance in P. mirabilis may result from increased expression of the bla VIM-1 carbapenemase gene through multiplication of its copy number.

Key concepts: Proteus mirabilis, Integron, Biology, Microbiology, Gene, Carbapenem, Proteus, Genetics

Related papers

Back to paper searchBrowse research topicsOriginal source
Increased Resistance to Carbapenems in Proteus mirabilis Mediated by Amplification of the bla VIM-1 -Carrying and IS 26 -Associated Class 1 Integron — Research Paper | ScholarLens