A truncated Tn916-like element in a clinical isolate of Enterococcus faecium
Related Experiment Video
Updated: Aug 15, 2026

A Duplex Digital PCR Assay for Simultaneous Quantification of the Enterococcus spp. and the Human Fecal-associated HF183 Marker in Waters
Published on: March 9, 2016
1Department of Microbiology and Immunology, Temple University School of Medicine, Philadelphia, Pennsylvania 19140.
Abstract:
A 58.7-kb nonconjugative plasmid (pKQ1) previously reported in a clinical isolate of Enterococcus faecium was found to contain both a tetM and an erythromycin resistance (erm) determinant. The plasmid contained a region homologous to the A, F, H, and G HincII fragments of Tn916. However, the 4.8-kb B fragment of Tn916 which contained the tetM determinant was replaced by a 7.3-kb fragment, and the 3.6-kb HincII C fragment of Tn916 was missing. An element homologous to Tn917 was juxtaposed to the truncated Tn916-like element. The Tn917-like element was similar in size to the erm transposon Tn917 as determined by a ClaI restriction digest which spanned approximately 99% of the transposon. When Bacillus subtilis or Streptococcus sanguis were transformed with pKQ1, no zygotically induced transposition of the tetM element was detected. Similarly no transposition of the Tn917-like element was detected.
Insights
This study characterizes plasmid pKQ1 from Enterococcus faecium, revealing a modified Tn916 element carrying tetM and a Tn917-like element conferring erythromycin resistance. Transposition of these resistance genes was not observed in tested bacteria.
Area of Science:
- Microbiology
- Molecular Biology
- Genetics
Background:
- Enterococcus faecium is a significant opportunistic pathogen.
- Antibiotic resistance in bacteria is a growing public health concern.
- Plasmids play a crucial role in the dissemination of antibiotic resistance genes.
Purpose of the Study:
- To characterize the genetic structure of the nonconjugative plasmid pKQ1.
- To investigate the organization of antibiotic resistance determinants within pKQ1.
- To assess the transposition potential of resistance elements on pKQ1.
Main Methods:
- Plasmid DNA isolation and characterization.
- Restriction enzyme digestion and fragment analysis (HincII, ClaI).
- Bacterial transformation experiments (Bacillus subtilis, Streptococcus sanguis).
Main Results:
- Plasmid pKQ1 (58.7 kb) harbors tetM and an erythromycin resistance (erm) determinant.
- pKQ1 contains a truncated Tn916-like element with a modified B fragment and a missing C fragment.
- A Tn917-like element, similar in size to Tn917, is adjacent to the truncated Tn916-like element.
- No zygotically induced transposition of tetM or the Tn917-like element was detected in transformed B. subtilis or S. sanguis.
Conclusions:
- Plasmid pKQ1 possesses a unique mosaic structure of Tn916 and Tn917-like elements.
- The tetM and erm determinants on pKQ1 appear to be stably maintained and do not exhibit transposition under the tested conditions.
- Understanding the genetic makeup of such plasmids is vital for tracking and controlling antibiotic resistance spread.
Related Concept Videos
Repressible Operon: trp Operon
Other Unique Bacteria
Bacterial Gastroenteritis
Clinical Significance of Antibiotic Resistance

