Welcome to the Department of Microbiology

This department is composed of 15 research groups and 4 project groups. We are characterized by excellence in enabling technologies within molecular and computational biology and a strong focus on curiosity driven basic science with a track record of ground-breaking research. Fundamental discoveries of enzyme activities have inspired a wide research portfolio spanning early development to aging and implications for human disease during the entire life course.

This strong focus on fundamental research has resulted in the section being awarded a Centre of excellence, Centre for Embryology and Healthy Development (CRESCO) that started 1st July 2023.

Our research strategy is aligned with the overall aims at Oslo University Hospital and Clinic of Laboratory Medicine. In addition we have priorities in three pillars; ground-breaking research, development of talent and innovation.

Head of department: Fredrik Müller
Head of research section: Hilde Loge Nilsen

News:

News about our researchers

Research groups:

RNA/DNA base modifications

Ingrun Alseth

Stem Cells, Ageing and Cancer

Lorena Arranz

Fungal and Bacterial Infections Research Group

Jørgen V. Bjørnholt

Cellular Responses to DNA Damage

Magnar Bjørås

Cell and tissue dynamics

Stig Ove Bøe

Genome and Epigenome Regulation in Embryo Development, Ageing and Disease

John Arne Dahl

Structural Biology and DNA repair

Bjørn Dalhus

Clinical Virology Research Group 

Susanne G. Dudman

Stem Cell Dynamics and RNA Regulation

Adam A. Filipczyk

Laboratory for Dynamic Gene Regulation

Arne Klungland

Virology Research Group

Mari Kaarbø 

Genome Instability in Ageing and Disease

Hilde L. Nilsen

Targeting tumors of central nervous system

Deo Prakash Pandey

Genome Dynamics

Tone Tønjum

Bacterial Defense Systems and Antimicrobial Resistance Group

James Booth and Emily Helgesen

News

OUS Researcher Awards 2026 - ceremony June 12th Excellent researcher awards to Kristina Hauge, Ida Lindeman and Nicola Pietro Montaldo

Three Oslo University Hospital scientists received prestigous awards for their outstanding research on June 12th 2026.
The major prize - the "Excellent Researcher Award" - went to Kristina Haugaa. 
Ida Lindeman and Nicola Pietro Montaldo both received the "Early Career Award".
The prize money - 400.000 and 200.000 NOK respectively - is earmarked for research activities.

Innovation funding for two researchers from the Department of Microbiology

Arranz (left) and Brunvoll
Arranz (left) and Brunvoll

The UiO Growth House help researchers to mature early-stage ideas. The University of Oslo has in 2026 allocated NOK 5 million for early-stage innovation projects in two categories.
Lorena Arranz, Leader of the Stem Cells, Ageing and Cancer group and Deputy Director of SFF CRESCO, has received NOK 400 000 for the test and further development phase of a succinate analogue suitable for therapeutic applications in cancer.
Sonja Hjellegjerde Brunvoll, Researcher in the Genome and Epigenome Regulation in Embryo Development, Ageing and Disease group, has received NOK 50 000 for her project ONCOFAST; Intermittent fasting during chemotherapy – a randomized feasibility study.

Project funded through prestigious programme: Norwegian researchers awarded major grant to uncover how cells remember starvation

Enserink and Knævelsrud
Enserink and Knævelsrud

A team of researchers led by Jorrit Enserink from Oslo University Hospital and Helene Knævelsrud from the University of Oslo has been awarded 40 million NOK from the Research Council of Norway to investigate a fundamental biological question: Can cells remember being starved, and does that memory change how they behave in the future?

The project, called Total Recall (Learn–Recall–Forget: Causal Circuits of Starvation Memory for Population Coherence in Homeostasis and Development), was funded through the prestigious "Toppforskere" programme, which supports research teams with the potential to become world-leading in their field.

New Nature Microbiology paper: Long-term HIV-1 remission achieved through allogeneic haematopoietic stem cell transplant from a CCR5Δ32/Δ32 sibling donor

Mari Kaarbø, Group leader of the Virology Research Group, and collaborators report a case of sustained HIV remission following stem cell transplantation from a CCR5Δ32/Δ32 donor.

This paper describes a 63-year-old man living with HIV who received such a transplant from his brother to treat myelodysplastic syndrome, a blood disorder. After the transplant, his blood and immune system were entirely replaced by his brother’s cells. Two years later, he stopped taking HIV medication.

Press release: SUMOylation inhibition drives an epigenetic "Switch" to reprogram fat cells, sugesting novel strategies to ameliorate metabolism

Patrizia Nothnagel (first author) and Pierre Chymkowitch (senior author)
Patrizia Nothnagel (first author) and Pierre Chymkowitch (senior author)

The group of Dr. Pierre Chymkowitch (Dept. of Microbiology, OUS and IBV, UiO), and their collaborators at NCMBM and IMB, have made a step forward to understanding how fat cells keep their identity and can be reprogrammed. Published in Nucleic Acids Research, the work demonstrates that a brief pharmacological inhibition of SUMOylation using the small molecule TAK-981, when combined with the PPARG agonist rosiglitazone, stably "imprints" a beige differentiation fate in human adipose stem cells. Unlike typical white fat cells that store energy, beige cells can burn fat to generate heat through a process called adaptive thermogenesis or beiging.

New EMBO Molecular Medicine paper: CDK12/CDK13 inhibition disrupts transcriptional elongation and replication fork progression in glioblastoma

Pandey group
Pandey group

Deo Prakash Pandey, leader of the "Targeting tumors of central nervous system" research group at the Department of Microbiology, and collaborators have identified a promising new therapeutic strategy for glioblastoma, the most common and aggressive malignant brain tumor in adults.
Glioblastoma cells, particularly glioblastoma stem cells, rely on abnormally high transcriptional activity driven by neurodevelopmental transcription factors. The study shows that these stem cells are selectively vulnerable to inhibition of the transcriptional cyclin-dependent kinases CDK12 and CDK13, while inhibition of other transcriptional kinases such as CDK7 and CDK9 results in broader, non-specific toxicity.

ClinVir joins the new EU-project ONWARD: Together we move forward!

Susanne Dudman
Susanne Dudman

This project aims to combat the most common cause of acute viral hepatitis, zoonotic hepatitis E, in a One Health perspective. More than 30 European countries participate with a total of 150 members joining.
Susanne Dudman is representing Norway and is leading work group 2, focusing on clinical management. The group aims to establish robust and comparable clinical trial frameworks, standardize outcome measurements, and support the identification and development of antiviral therapies.