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Testing the Role of Multicopy Plasmids in the Evolution of Antibiotic Resistance
Published on: May 2, 2018
Imipenem-resistance in Serratia marcescens is mediated by plasmid expression of KPC-2
1Department of Laboratory, Qingdao Municipal Hospital, Qingdao, China. li_li_1212@163.com.
Objective:
Imipenem is a broad-spectrum carbapenem antibiotic with applications against severe bacterial infections. Here, we describe the identification of imipenem-resistant Serratia marcescens in our hospital and the role of plasmid-mediated KPC-2 expression in imipenem resistance.
Materials And Methods:
We used the modified Hodge test to detect carbapenemase produced in imipenem-resistant strains.
Results:
His resistance can be transferred to E. coli in co-culture tests, which implicates the plasmid in imipenem resistance. PCR amplification from the plasmid identified two products consistent with KPC-2 of 583 and 1050 bp that were also present in E. coli after co-culture. The restriction pattern for both plasmids was identical, supporting the transfer from the S. marcescens isolate to E. coli. Finally, gene sequencing confirmed KPC-2 in the plasmid.
Conclusions:
Due to the presence of KPC-2 in the imipenem-resistant S. marcescens, we propose that KPC-2 mediates antibiotic resistance in the S. marcescens isolate.
Insights
We identified imipenem-resistant Serratia marcescens strains in our hospital. Plasmid-mediated Klebsiella pneumoniae carbapenemase-2 (KPC-2) expression was found to be responsible for this antibiotic resistance.
Area of Science:
- Microbiology
- Infectious Diseases
- Antibiotic Resistance
Background:
- Imipenem is a critical carbapenem antibiotic for severe bacterial infections.
- The emergence of antibiotic resistance poses a significant threat to public health.
Purpose of the Study:
- To identify the mechanism of imipenem resistance in Serratia marcescens.
- To investigate the role of plasmid-mediated carbapenemase expression.
Main Methods:
- Modified Hodge test was used to detect carbapenemase production.
- Plasmid transfer was assessed using co-culture experiments with E. coli.
- PCR amplification and gene sequencing were employed to identify the specific carbapenemase.
Main Results:
- Imipenem-resistant Serratia marcescens was identified.
- Plasmid-mediated transfer of resistance to E. coli was confirmed.
- PCR and sequencing identified the presence of KPC-2 carbapenemase in the resistant strains.
Conclusions:
- The study proposes that plasmid-mediated KPC-2 expression is responsible for imipenem resistance in the identified Serratia marcescens isolate.
- This finding highlights the importance of monitoring carbapenemase-producing Enterobacteriaceae.
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