Job Description

Mikrobiologie

25.025 Stunden

auf 12 Monate befristet

ab 01.01.2026

Eingruppierung gemäß TV-L

Bewerbungsfrist 24.10.2025

Universitätsklinikum Erlangen

Microbiological Institute - Clinical Microbiology, Immunology and Hygiene

Prof. Dr. med. Roland Lang

Wasserturmstraße 3/5

91054 Erlangen

Ansprechperson bei Fragen

Prof. Dr. med. Roland Lang

Group Leader and Deputy Director of the Institute

+49 (0)9131 85 - 46904

PhD position in Infection Immunology (m/f/d)

Veröffentlicht seit:

03.10.2025

Job-Nr.:

11435

Ansprechperson bei Fragen

Prof. Dr. med. Roland Lang

Group Leader and Deputy Director of the Institute

+49 (0)9131 85 - 46904

Anschrift

Universitätsklinikum Erlangen

Microbiological Institute - Clinical Microbiology, Immunology and Hygiene

Prof. Dr. med. Roland Lang

Wasserturmstraße 3/5

91054 Erlangen

PhD position in Infection Immunology (m/f/d)

Veröffentlicht seit:

03.10.2025

Job-Nr.:

11435

Universitätsklinikum Erlangen

Microbiological Institute - Clinical Microbiology, Immunology and Hygiene

Prof. Dr. med. Roland Lang

Wasserturmstraße 3/5

91054 Erlangen

Ansprechperson bei Fragen

Prof. Dr. med. Roland Lang

Group Leader and Deputy Director of the Institute

+49 (0)9131 85 - 46904



Klingt spannend?

Das sind wir:

The laboratory „Balancing innate immunity“ (Prof. Dr. med. Roland Lang) at the Institute of Clinical Microbiology, Immunology and Hygiene of the University Hospital Erlangen offers a PhD position to investigate the function of the immunometabolite itaconate in macrophage anti-microbial activity.



Research in the Lang lab investigates how the immune system generates resistance to infection while avoiding excessive inflammation. This includes a need for efficient sensing of microbes by macrophages, generating inflammatory cytokines that direct adaptive immune responses, and regulatory mechanisms to achieve resolution of inflammation.



In collaboration with the lab of Prof. Anja Lührmann at our institute, we have investigated the host response to the intracellular bacterium Coxiella burnetii and established a mouse model to identify which immune pathways determine persistence or resolution of Q fever. The generation of the metabolite itaconate by activated macrophages is essential to restrain replication of Coxiella burnetii in macrophages and to contain early infection in vivo.



Lab homepage



https://www.mikrobiologie.uk-erlangen.de/en/research/research-groups/research-group-of-prof-roland-lang/publications/



Relevant publications



Kohl, L., Hayek, I., Daniel, C., Schulze-Luhrmann, J., Bodendorfer, B., Lührmann, A., and Lang, R. (2019). MyD88 Is Required for Efficient Control of Coxiella burnetii Infection and Dissemination. Frontiers in immunology 10, 165. Doi: 10.3389/fimmu.2019.00165

Kohl, L., Siddique, M., Bodendorfer, B., Berger, R., Preikschat, A., Daniel, C., Olke, M., Liebler-Tenorio, E., Schulze-Luehrmann, J., Mauermeir, M., et al. (2023). Macrophages inhibit Coxiella burnetii by the ACOD1-itaconate pathway for containment of Q fever. EMBO Mol Med 15, e15931. Doi: 10.15252/emmm.202215931

Lang, R., and Siddique, M. (2024). Control of immune cell signaling by the immuno-metabolite itaconate. Frontiers in immunology 15. Doi: 10.3389/fimmu.2024.1352165

Siddique, M., Kellermeier, F., Olke, M., Zhao, M., Bussow, K., Oefner, P.J., Lührmann, A., Dettmer, K., and Lang, R. (2024). Divergent effects of itaconate isomers on Coxiella burnetii growth in macrophages and in axenic culture. Frontiers in immunology 15, 1427457. Doi: 10.3389/fimmu.2024.1427457

Your tasks:

The present DFG-funded project addresses the mechanisms underlying the protective effect of the ACOD1-itaconate pathway in C. burnetii infection. We aim to dissect the molecular basis of regulated uptake and intracellular transport of itaconate in infected macrophages and will address how itaconate alters anti-microbial capacities of macrophages.

The methods employed to investigate the mechanisms will comprise in vitro infection experiments and sgRNA-based analysis of itaconate production and transport, as well as infection experiments in conditional knockout mice with cell type-specific gene deletions in the ACOD1-itaconate pathway.

Readout systems will include multi-color flow cytometry, ELISA and multiplex cytokine analyses, protein modification and RNAseq analyses.

Comments:

Applications need to include informative letter of motivation and CV, 2-3 letters of recommendation, and copies of transcript of records, certificates (high school diploma, bachelor and master studies)

Essential experience/qualifications:

We are looking for highly motivated candidates holding a Master degree in the Life Sciences with a strong background in immunology, molecular biology and infection biology.

Practical experience in cell culture, flow cytometry and mouse models is advantageous.

We offer:

Position will be paid according to the German salary guidelines (TV-L)

Attractive PhD thesis topic in highly relevant infection and immunity research area

Stimulating research environment at the Microbiological Institute and the iMED campus

Membership in the structured educational PhD program of Life@FAU graduate school

Thorough and qualified introduction into project and supportive working group

Fixed-term contract for up to 36 months



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