Projects per year
Abstract
Resistance to ciprofloxacin, a treatment choice for Salmonella infections, has increased dramatically in recent years in particular in serotype Salmonella Derby with most of strains carrying chromosome-encoded multiple plasmid-mediated quinolone resistance (PMQR) genes. In this work, we discovered a conjugative plasmid, pSa64-96kb, in a Salmonella Derby isolate, namely Sa64, which could extract and fuse to a multiple drug resistance (MDR) DNA fragment containing two PMQR genes, aac(6’)-Ib-cr, and qnrS2 located on the chromosome of the Salmonella strain. This process led to the formation of a new 188 kb fusion plasmid, which could be then subsequently transmitted to recipient strain Escherichia coli J53. The chromosomal MDR DNA fragment was shown to be flanked by one copy of IS26 element at each end and could be excised from the chromosome to form circular intermediate, which was then fused to pSa64-96kb and form a single plasmid through IS26 mediated homologous recombination. The role of IS26 on enhancing the efficacy of fusion and transmission of this chromosomal MDR DNA fragment was further proven in other Salmonella strains. These findings showed that dynamic interaction between specific chromosomal fragment and plasmids may significantly enhance resistance development and transferability of mobile resistance-encoding elements among bacterial pathogens.
| Original language | English |
|---|---|
| Article number | 556227 |
| Journal | Frontiers in Microbiology |
| Volume | 11 |
| Online published | 18 Sept 2020 |
| DOIs | |
| Publication status | Published - Sept 2020 |
Research Keywords
- chromosomal fragment
- ciprofloxacin resistance
- conjugative helper plasmid
- PMQR genes
- Salmonella
Publisher's Copyright Statement
- This full text is made available under CC-BY 4.0. https://creativecommons.org/licenses/by/4.0/
Fingerprint
Dive into the research topics of 'Transmission of Chromosomal MDR DNA Fragment Encoding Ciprofloxacin Resistance by a Conjugative Helper Plasmid in Salmonella'. Together they form a unique fingerprint.Projects
- 1 Finished
-
CRF: Development of Novel Inhibitors Targeting the Resistance Mechanisms of Clinical Superbugs
CHEN, S. (Principal Investigator / Project Coordinator), CHAN, K. F. (Co-Principal Investigator), Hao, Q. (Co-Principal Investigator), LI, X. (Co-Principal Investigator) & MA, E.D.-L. (Co-Principal Investigator)
30/06/17 → 29/06/21
Project: Research
Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver