Related Experiment Video
Updated: Aug 11, 2026

Multiplex PCR Assay for Typing of Staphylococcal Cassette Chromosome Mec Types I to V in Methicillin-resistant Staphylococcus aureus
Published on: September 5, 2013
Characterization of a novel type of MLSB resistance plasmid from Staphylococcus saprophyticus carrying a
Tomasz Hauschild1, Petra Lüthje, Stefan Schwarz
1University of Bialystok, Institute of Biology, Department of Microbiology, 15-950 Bialystok, Swierkowa 20 B, Poland.
Abstract:
An erm(C)-carrying plasmid of unusual size and restriction map, designated pSES22, was identified in a Staphylococcus saprophyticus strain and sequenced completely. Constitutive expression of the erm(C) gene from pSES22 is based on a novel 22-bp tandem duplication in the erm(C) translational attenuator. Comparative analysis of the deduced Erm(C) amino acid sequence revealed that Erm(C) from pSES22 - together with an Erm(C) methylase from S. hyicus - represented a separate branch in the homology tree of Erm(C) methylases. Structural comparisons showed that plasmid pSES22 differed distinctly from all other completely sequenced erm(C)-carrying resistance plasmids. However, pSES22 was similar to several members of a diverse group of small plasmids, all of which carried closely related plasmid backbones consisting of the genes repU and pre/mob, but differed in their resistance genes.
Insights
A novel Staphylococcus plasmid, pSES22, carrying the erm(C) gene was identified. Its unique structure and a novel duplication in the erm(C) gene explain constitutive expression and distinctness from other resistance plasmids.
Area of Science:
- Microbiology
- Molecular Biology
- Genetics
Background:
- Antibiotic resistance is a growing public health concern.
- Plasmids are key vehicles for the dissemination of antibiotic resistance genes.
- Staphylococcus species are significant human pathogens, often carrying resistance plasmids.
Purpose of the Study:
- To characterize a novel erm(C)-carrying plasmid, pSES22, identified in Staphylococcus saprophyticus.
- To elucidate the genetic basis for constitutive erm(C) gene expression from pSES22.
- To compare the structure of pSES22 with other known erm(C) resistance plasmids.
Main Methods:
- Complete sequencing of the pSES22 plasmid.
- Comparative analysis of the erm(C) gene and its regulatory elements.
- Bioinformatic analysis of plasmid backbone genes (repU, pre/mob).
- Phylogenetic analysis of deduced Erm(C) amino acid sequences.
Main Results:
- pSES22 possesses an unusual size and restriction map compared to other erm(C) plasmids.
- A novel 22-bp tandem duplication in the erm(C) translational attenuator confers constitutive expression.
- Erm(C) from pSES22 forms a distinct branch in the homology tree of Erm(C) methylases.
- pSES22 shares a plasmid backbone with other small plasmids but differs in its resistance gene.
Conclusions:
- pSES22 represents a unique erm(C)-carrying plasmid with a novel mechanism for constitutive gene expression.
- The findings highlight the diversity of erm(C) plasmids and their potential for dissemination.
- Understanding plasmid evolution and structure is crucial for combating antibiotic resistance.
More Related Videos
07:10A Fluorescence-based Method to Study Bacterial Gene Regulation in Infected Tissues
Published on: February 19, 2019
05:06Characterizing Multidrug Efflux Systems in Acinetobacter baumannii Using an Efflux-Deficient Bacterial Strain and a Single-Copy Gene Expression System
Published on: January 5, 2024
Related Concept Videos
Mechanism of Antibiotic Resistance in MRSA
Clinical Significance of Antibiotic Resistance
Plasmids
Development of Antibiotic Resistance
Antibiotic Selection
Conjugation