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Kenn Gerdes

Kenn Gerdes

Professor

Gerdes Research Group

  • Birgitte Haugan Ullerup, PA and Center administrator
  • Solveig Walløe Harpøth, PA and Center administrator (maternity cover)
  • Sidsel Henriksen, Lab Manager
  • Ragnhild Jørgensen Bager, post doc
  • Kristoffer Winther, post doc
  • Mohammad Roghanian, post doc
  • Szabolcs Semsey, post doc
  • Alexander Harms, post doc
  • Yong Zhang, post doc
  • Farshid Jalalvand, post doc
  • Kirtimaan Syal, post doc
  • Georgia Hann, PhD student
  • Kathryn Turnbull, PhD student
  • Emilie Søndberg, PhD student
  • Stine Vang Nielsen, PhD student
  • Cinzia Fino, PhD student
  • Meiqin Zhang, Research assistent
  • Simon Gerbild, Master student

Ambitious, potential PhD-students and Post Doc are encouraged to send their CV to Kenn Gerdes 

Current Collaborators

  • Nick Thomson, Sanger Institute, UK
  • Ditlev Brodersen, Aarhus University
  • David Clarke, University College Cork, Ireland
  • Christoph Dehio, Biozentrum, Basel, Switzerland
  • Vasili Hauryliuk, Umeå University, Sweden
  • Boris Macek, University of Tübingen, Germany
  • Kim Sneppen, Niels Bohr Institute, University of Copenhagen
  • Namiko Mitarai, Niels Bohr Institute, University of Copenhagen

 

Introduction to Current Research

The overarching research themes in the Gerdes group are Bacterial Stress Responses and Antibiotic Multidrug Tolerance (Persistence). Research within these fields facilitated the establishment of a research centre funded by the Danish National Research Foundation and the Novo Nordisk Foundation called Centre for Bacterial Stress Responses and Persistence (BASP). This long-term funding enables us to attack difficult but important basic research questions.

Most bacteria live in constantly changing environments and, accordingly, have evolved highly sophisticated regulatory mechanisms that allow them to withstand stressful conditions. In particular, almost all bacteria depend on the ubiquitous regulatory molecules tetra and penta-guanosine phosphate, collectively called (p)ppGpp or Magic Spot, for the survival in the environment and during infections. Thus, the (p)ppGpp-mediated response is required for almost all pathogenic bacteria to be virulent, and thus our basic research will lead to an increased general understanding of bacterial survival and virulence mechanisms.   

Magic Spot was discovered in experiments with the model organism E. coli undergoing amino acid starvation elicits the “stringent response”. In that response, (p)ppGpp reprograms cellular metabolism from rapid to slow growth or dormancy. Here, (p)ppGpp increases dramatically in concentration and profoundly influences gene expression such that the cells manage to adapt to and survive the limited nutrient supply. Importantly, rRNA synthesis is severely curtailed while transcription of amino acid biosynthetic operons is stimulated. Thus, a primary role of (p)ppGpp is to adjust cell growth to the available nutrient resources. However, (p)ppGpp affects many other cellular processes, such as replication, transcription and protein turnover, either directly or indirectly. Stunningly, even though (p)ppGpp has been known for almost 50 years, it is not yet understood how its synthesis is controlled. Magic Spots is synthesized and hydrolysed by the bifunctional Rel enzymes (RelA and SpoT) that are regulated by a number of factors including ribosome-bound tRNA and essential GTPases. However, at the molecular level surprisingly little is known about how Rel enzymes are regulated. As described further below, a long-term goal of our research is to understanding how the enzymatic activities of RelA and SpoT are regulated and how (p)ppGpp contributes to bacterial virulence and persistence (multidrug tolerance).

 

Current Research Projects

Kristoffer Skovbo Winther

RelA [(p)ppGpp Synthetase I] of E. coli. We use UV-cross-linking and high-throughput sequencing of RNA (CRAC) to map the interactions between RelA, tRNA and ribosomal RNA in order to understand the molecular mechanism underlying activation of RelA synthetic activity. 

 

 

Toxin – Antitoxins

(Kathryn Turnbull)

Usually, TA modules code for two components, a toxin that reversibly inhibits cell growth and an antitoxin that counteracts toxin activity; three types of TA loci have been identified. Type I and type III TA loci encode small RNAs that counter the toxins at the translational and posttranslational levels, respectively. Toxins encoded by type II TA loci are inhibited by protein antitoxins via direct protein – protein interaction. Owing to sequence conservation of the toxins, type II TA loci have been divided into families that are broadly conserved in bacteria, or in some cases even in both bacteria and archaea. Thus, members of the relBEvapBC, and hicAB families are abundant in these two domains of

Both of these gene modules function in persistence but we do not exclude that the genes have other functions as well.

(p)ppGpp and Toxin – Antitoxins of Photorhabdus luminescence

(Ragnhild Jørgensen Bager in collaboration with David Clarke, Cork, Ireland)

P. luminescens is a Gram-negative belonging to the family Enterobacteriaceae. Being both a pathogen of a wide range of insects, as well as mutualistic associated with nematodes from the family Heterorhabditis, the bacterium is an excellent model system in which to study the genetics of both mutualism and pathogenicity. Similar to M. tuberculosis, the P. luminescence has a cohort of TA genes. We are now validating some of the TA modules experimentally. We are also investigating the effects of deleting different regulatory genes (relAspoTlonppkppx and TAs) on various phenotypes of this insect pathogen, primarily the effects on its persistence, symbiosis and virulence.

 

(p)ppGpp and Toxin – Antitoxins of Photorhabdus luminescence

(Ragnhild Jørgensen Bager in collaboration with David Clarke, Cork, Ireland)

P. luminescens is a Gram-negative belonging to the family Enterobacteriaceae. Being both a pathogen of a wide range of insects, as well as mutualistic associated with nematodes from the family Heterorhabditis, the bacterium is an excellent model system in which to study the genetics of both mutualism and pathogenicity. Similar to M. tuberculosis, the P. luminescence has a cohort of TA genes. We are now validating some of the TA modules experimentally. We are also investigating the effects of deleting different regulatory genes (relA, spoT, lon, ppk, ppx and TAs) on various phenotypes of this insect pathogen, primarily the effects on its persistence, symbiosis and virulence.

 

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