Leise Riber
Lektor
Microbial Ecology and Biotechnology
Thorvaldsensvej 40
1871 Frederiksberg C
Research interests
My main focus is on finding new strategies to limit the occurrence of plasmid-borne spread of antimicrobial resistance. The spread of antimicrobial resistance among bacterial populations is mainly due to the acquisition of resistance genes located on transferable plasmids obtained through horizontal gene transfer. New ways of reducing the spread and selection of resistance therefore include the disturbance of the dynamics of plasmid transfer and stability. Current work areas include studying molecular mechanisms involved in horizontal gene transfer and plasmid stability, as well as baseline studies of the prevalence and dissemination of resistance plasmids in complex natural environments. Areas of expertise include various techniques within molecular microbiology and bacterial genetics. Main focus is on construction of bacterial reporter strains and cloning of conjugative plasmids using mini-mu and Tn7 based transposon systems for studies of horizontal gene transfer (HGT) and plasmid dynamics in complex environments. Additionally, HGT studies include expertise within cell counting using flow cytometry as well as cell sorting for 16S sequencing using Fluorescence activated cell sorting (FACS).
Education
2003-2007 Ph.D., (Molecular Microbiology). Roskilde University, Roskilde.
1996-2003 Cand. Polyt., (Chemistry, Biotechnology). Technical University of Denmark, Lyngby.
Employment
2010- Post-doctoral Fellow, (Molecular Microbiology). University of Copenhagen, Institute of Biology, KU-BIO, Copenhagen.
2008-2010 Post-doctoral Fellow, (Molecular Microbiology and Food Microbiology). National Food Institute, Technical University of Denmark, DTU-FOOD, Mørkhøj.
2006-2007 Post-doctoral Fellow, (Molecular Microbiology). Roskilde University, Roskilde.
Publications and Presentations
5 publications in international peer reviewed journals; about 10 contributions to
conferences (posters, oral presentations), workshops, etc. Once receiver of the
Scholarship “Carlsbergs Mindelegat for Brygger J.C. Jacobsen”.
1. Charbon, G., et al., Suppressors of DnaA(ATP) imposed overinitiation in Escherichia coli. Mol Microbiol. 2011. 79(4): p. 914-28.
2. Gronlund, H., et al., Microarray-based genotyping of Salmonella: inter-laboratory evaluation of reproducibility and standardization potential. Int J Food Microbiol. 2011. 145: p. S79-85.
3. Riber, L., et al., Loss of Hda activity stimulates replication initiation from I-box, but not R4 mutant origins in Escherichia coli. Mol Microbiol, 2009. 71(1): p. 107-22.
4. Riber, L. and A. Lobner-Olesen, Coordinated replication and sequestration of oriC and dnaA are required for maintaining controlled once-per-cell-cycle initiation in Escherichia coli. J Bacteriol, 2005. 187(16): p. 5605-13.
5. Riber, L., et al., Hda-mediated inactivation of the DnaA protein and dnaA gene autoregulation act in concert to ensure homeostatic maintenance of the Escherichia coli chromosome. Genes Dev, 2006. 20(15): p. 2121-34.
Uddannelse
Cand polyt, PhD
ID: 17515397
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Complete genome sequence of the cystic fibrosis pathogen Achromobacter xylosoxidans NH44784-1996 complies with important pathogenic phenotypes
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An improved method for including upper size range plasmids in metamobilomes
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Type 3 fimbriae encoded on plasmids are expressed from a unique promoter without affecting host motility, facilitating an exceptional phenotype that enhances conjugal plasmid transfer
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