Characterization of pTS14, an IncF2:A1:B1 Plasmid Carrying tet(M) in a Salmonella enterica Isolate

Ying-Ying Liu1, Xiao-Kang Liu1, Xiao-Die Cui1

  • 1College of Animal Husbandry and Veterinary Science, Henan Agricultural University, Zhengzhou, China.

Insights

A novel 119-kb plasmid, pTS14, carrying the tetracycline resistance gene tet(M) was identified in Salmonella enterica. This highly stable plasmid also harbors additional resistance genes and enhances bacterial survival under stress, posing a clinical threat.

Area of Science:

  • Microbiology
  • Genetics
  • Molecular Biology

Background:

  • Antimicrobial resistance is a growing global health concern.
  • Plasmids are key vehicles for the dissemination of antibiotic resistance genes.
  • Salmonella enterica is an important foodborne pathogen.

Purpose of the Study:

  • To characterize the genetic and biological features of the tet(M)-harboring plasmid pTS14 in Salmonella enterica strain S14.
  • To assess the stability and survival capabilities conferred by plasmid pTS14.
  • To evaluate the potential threat posed by this plasmid lineage.

Main Methods:

  • Plasmid identification using conjugation, pulsed-field gel electrophoresis (PFGE), and Southern hybridization.
  • Complete plasmid sequencing to determine genetic content.
  • Biological assessments including stability, growth kinetics, and starvation survival experiments.

Main Results:

  • A 119-kb IncF2:A1:B1 conjugative plasmid, pTS14, carrying tet(M) was identified in Salmonella enterica ST3007.
  • Plasmid pTS14 harbors a novel transposon Tn6709 and multiple resistance genes: tet(B), tet(D), strAB, sul2, and blaTEM-1b.
  • pTS14 demonstrated high stability in E. coli J53 and enhanced transconjugant survival under starvation stress.

Conclusions:

  • The tet(M)-bearing IncF2 epidemic plasmid lineage can facilitate the spread of tet(M) and other resistance genes through coselection.
  • Plasmid pTS14 represents a significant threat to clinical treatment regimens due to its stability and resistance gene content.
  • Further research is needed to understand the full epidemiological impact of such plasmids.