Survey
* Your assessment is very important for improving the work of artificial intelligence, which forms the content of this project
* Your assessment is very important for improving the work of artificial intelligence, which forms the content of this project
Genetics Department of Genetics, Microbiology and Toxicology People • Professors: – Elisabeth Haggård – Ingrid Faye – Per Palsbøll • Associate Professor (Lektor): – Anders Nilsson • Assistant Professor (FoA): – Mary Hunt • Research Associate: – Martine Bérubé • Post doctoral researcher: – Katharina Slätis • 10 PhD and 3 MSc students Mary Hunt’s group: Endocannabinoids Induce sleep Thermoregulation Pain suppression Appetite control Cannabis Endocannabinoids An example of the newly identified lipid molecules N-arachidonylglycine detected in various organs in the body How are these lipids produced? How are these processes regulated at the genetic level? Signalling pathways regulated by these lipids? Ingrid Faye current projects Innate immune responses in the malaria mosquito triggered by: A. Pattern molecules (PAMPs)/ antigens from the human malaria parasite (Plasmodium falciparum) 1. Receptors? 2. Signalling pathways? 3. Human/vector common denominators the response? A. Bacterial isolates from the midgut of Anopheles mosquitoes to be used in paratransgenics 1. Field isolate – Thorsellia anophelis 2. Lab isolate – Elisabethkingia anophelis Paratransgenics - main steps • Screen for gene encoded anti-parasitic peptides/proteins • Isolate midgut bacteria • Test anti-parasitic efficacy of peptides • Characterize bacteria • Genetically label • Re-establish in the gut • Test efficacy of system in vivo • Test in the semi-field conditions Research group & funding • PhD students – Karolina ErikssonGonzales – Bo Lindberg • Masters Students – Steven Lewis – Holly Matthews • EU Network – COST Action FA0701 – BioMalPar II • Funding – EU INFRAVEC – ARC Elisabeth Haggård PhD students: Lina Sylwan, Sridhar Mandali, Wilhelmina Sehlén Project 1. Phage site-specific integrases (Int) and their evolution as tools for directed gene insertions into unmodified eukaryotic cells. •Structure-function analysis of the integrases of P2-like phages. •Target (attB) requirements. •Efficiency and specificity of insertions in human cells. Phage attL Int IHF attP IHF Int Cox attR attB Target Project 2. Molecular characterization of the simple, but efficient, molecular switches in the P2 phage family that controls lytic versus lysogenic growth cycles. •3-D structure of the two repressors, C and Cox, controlling the switch (collaboration with T. Massad, K. Scaar, P Stenmark, biochemistry). •Amino acids and nucleotides involved in repressor specificity •Fluctuation analysis of the switch in the lysogenic state. C Pe Lytic C Lysogenic cox Pc - Cox Anders Nilsson, GMT Evolution of P2-like phages Phage therapy Phylogenetic relationships between single genes, as well as groups of genes, from different taxa reveal significant patterns in phage genome evolution and phage - host coevolution. A common antibiotic multiresistant phenotype of bacteria depends on horizontally transferred extended-spectrum β-lactamase (ESBL) plasmids. ESBL Klebsiella pneumoniae outbreaks are hazardous and hard to deal with in hospitals. Phylogenies of P2-like phage genes, and gene clusters, in γ-proteobacteria. Differentiation and distribution of P2-like phages in Escherichia and Salmonella strain collections. Isolation of phages that lyse Klebsiella pneumoniae strains. Optimisation of compilations of phages for lysis efficacy on Klebsiella pneumoniae expressing multiresistant ESBL phenotypes. ↓ ↓ • • • Are P2-like phage genomes modular? • What is the relative importance of different evolutionary mechanisms e.g. horizontal transfer of genes, recombination etc? • Coevolution and host shifting of P2-like phages - hosts? Ph D student Hanna Nilsson Lic thesis (2009): Differentiation and distribution of P2-like phages. What is the efficacy of single lytic phages on different Klebsiella isolates (strains, serotypes)? Is a mix of a few lytic phages a good candidate for phage therapy of ESBL Klebsiella pneumoniae. M Sc student (60 hp) Harald Eriksson Palsbøll Lab: Genetics in evolution, ecology, and conservation People Current funding • Research Associate Martine Bérubé • US NSF • Ph student Morten Tange Olsen • US MMC • PhD student JeanLuc Tison • M Sc student Laetitia Schmid • US NMFS • NV • Norwegian MRI • IWC Examples of ongoing projects • • • • • Climate change The micro-evolutionary effects of annual Polar sea ice dynamics in ringed seal (w Danish EPA and Norwegian Polar Institute) Community genetics The evolutionary co-dynamics of Polar bears and their prey; ringed and bearded seals (w Norwegian Polar Institute) Evolutionary/molecular genetics Contradicting signatures of population size changes in mtDNA (w GNI, MICS and CCS) Conservation genetics Recent and past changes in abundance, population structure and genetic diversity of large whales in the North Atlantic and Antarctic (w NMFS, MRIs, CCS and MICS, GNI, Oslo U and Cph U) Population genetics Mate choice and MHC, transmission and fitness consequences of seasonal site fidelity (w NMFS and CCS) Thank You!