• Skip navigation
  • Skip to navigation
  • Skip to the bottom
Simulate organization breadcrumb open Simulate organization breadcrumb close
DFG Research Training Group 2740 Immunomicrotope –
  • FAUTo the central FAU website
Suche öffnen
  • Campo
  • StudOn
  • FAUdir
  • Jobs
  • Map
  • Help

DFG Research Training Group 2740 Immunomicrotope –

Navigation Navigation close
  • 2nd International Conference “ImmunoMicroTope”
  • Research
    • Project areas
      • Project area A “Micromilieu”
      • Project area B „Metabolism“
    • Publications relevant to the RTG 2740
    • Latest Publications
    • Awards
    Portal Research
  • Program
    • Curriculum
      • RTG 2740-specific training measures
        • Lectures, seminars and research meetings
        • Workshops and practical courses
        • Annual and other scientific events
      • Training in general professional and transferable skills
      • Measures to promote national and international networking
    • Organization
    Portal Program
  • About us
    • Doctoral students
    • Associated Doctoral students
    • Medical Doctoral students
    • Principal Investigators
    • Associated Principal Investigators
    • Coordinator
    • Executive Board
    • External Advisory Board
    Portal About us
  • Open positions
  • How to apply
  1. Home
  2. Research
  3. Project areas
  4. Project area A “Micromilieu”
  5. A3: Induction and regulation of Coxiella burnetii persistence by microenvironmental factors

A3: Induction and regulation of Coxiella burnetii persistence by microenvironmental factors

In page navigation: Research
  • Project areas
    • Project area A “Micromilieu”
      • A1: Control of Citrobacter rodentium by oxygen-dependent B cell regulation
      • A2: Regulation of local tissue oxygenation in cutaneous leishmaniasis
      • A3: Induction and regulation of Coxiella burnetii persistence by microenvironmental factors
      • A4: The regulatory role of fibroblastic reticular cells during intestinal bacterial infections
      • A5: Impact of microenvironmental factors on neutrophil effector functions directed against Salmonella (S.) enterica serovar Typhimurium
      • A6: Eosinophils shape the tissue micro milieu and immune response in cutaneous leishmaniasis
      • A7: Characterization and mathematical modeling of the STAT6-regulated micro milieu in response to Nippostrongylus (N.) brasiliensis infections
    • Project area B "Metabolism"
  • Publications relevant to the RTG 2740

A3: Induction and regulation of Coxiella burnetii persistence by microenvironmental factors

A3: Induction and regulation of Coxiella burnetii persistence by microenvironmental factors

Coxiella (C.) burnetii is the causative agent of the zoonotic disease Q fever, which can be either acute or chronic. While acute Q fever is a flu-like illness, chronic Q fever mainly manifest as a potentially life-treating endocarditis month or years after primary infection. The period prior outbreak of chronic Q fever is characterized by bacterial persistence, a physiologically dormant state that can cause relapsing infections and antibiotic resistance. Currently, it is unknown how C. burnetii persistence is induced or regulated.

We hypothesize that micromilieu factors are decisive for the outcome of C. burnetii infection. Indeed, host cell metabolites influences C. burnetii infection. Thus, the TCA metabolite citrate support bacterial replication, while itaconate has anti-bacterial activity. In addition, our results suggest that a micromilieu with reduced oxygen availability (hypoxia) induces C. burnetii persistence. We are currently investigating how hypoxia influences the host cell metabolism and immune response during infection. Furthermore, we are characterizing the state of bacterial persistence. Thus, we are performing EM analysis, qRT-PCR and sequencing experiment and antibiotic resistance assays. In addition, we are investigating the ability of persistent bacteria to infect cells and resist elimination by the host cells

 

Lührmann Schmema

In macrophages C. burnetii are unable to replicate under hypoxic conditions. Hypoxia induces the stabilization of HIF1α, which in turn reduces the activation of STAT3. This leads to reduction of the TCA metabolite citrate, and a subsequent inhibition of C. burnetii replication (Hayek et al. 2019, Cell Reports). In contrast, C. burnetii replicates equally well in normoxic and hypoxic endothelial cells. The underlying reason is unclear.

Supervisor

Anja Lührmann

Prof. Dr. rer. nat. Anja Lührmann

Wasserturmstr. 3
91054 Erlangen
  • Phone number: +49 9131 85-32577
  • Email: anja.luehrmann@uk-erlangen.de
  • Website: http://www.mikrobiologie.uk-erlangen.de/
More › Details for Anja Lührmann

 

Universitätsklinikum Erlangen
Mikrobiologisches Institut

Wasserturmstr. 3/5
91054 Erlangen
  • Imprint
  • Privacy
  • Accessibility
  • Facebook
Up