Project Details
SFB 900: Chronic Infections: Microbial Persistence and its Control
Subject Area
Medicine
Term
from 2010 to 2022
Website
Homepage
Project identifier
Deutsche Forschungsgemeinschaft (DFG) - Project number 158989968
From birth on, human beings are colonized by a multitude of microorganisms that are able to persist in various niches of the human body over the lifetime of the colonized individual. The relationship between man and his microbiological ‘tenants’ is usually of a symbiotic nature. However, this symbiotic relationship can fail when certain bacterial species acquire new, pathogenic, traits or a stable, mutually beneficial co-existence of man and microbe cannot be established or maintained on account of genetically determined or acquired deficiencies in the host’s immune system. Persisting microorganisms are thus both ‘friend’ and ‘foe’ and differ fundamentally in their biological behaviour from microbes that infect humans or animals only in a transient manner and cause acute infectious disease. Where they are the cause of disease, their ability to persist creates a particular therapeutic challenge, as conventional therapeutic strategies aimed at curbing their replication or proliferation are usually not able to eradicate the infection and often only ‘buy time’. It is therefore the aim of collaborative research centre ‘Chronic Infections: Microbial Persistence and its Control’ to further advance our understanding of why, and how, chronic bacterial and viral pathogens persist, and how a better understanding of the mechanisms involved in microbial persistence can provide new approaches to therapy. CRC conducts research into several mechanisms of microbial persistence, in particular the ability of the pathogen to evolve in the infected host, thereby adapting itself to different habitats, immune pressure or selection by antimicrobial agents, its interaction with different immune sensing and effector mechanisms, and its ability to exploit intracellular pathways to promote its persistence in the infected cell.
DFG Programme
Collaborative Research Centres
Completed projects
- A01 - Genome and population dynamics during chronic infection with Helicobacter pylori (Project Head Suerbaum, Sebastian )
- A02 - Chronic Pseudomonas aeruginosa infections in cystic fibrosis: pathogen microevolution and host genetic predisposition (Project Head Tümmler, Burkhard )
- A03 - Biofilm formation in response to fluctuating environmental conditions in Pseudomonas aeruginosa: a global genetic approach (Project Head Häußler, Susanne )
- A04 - Mechanisms of host-bacteria homeostasis on the intestinal epithelium (Project Head Hornef, Mathias Walter )
- A05 - Cure of chronic hepatitis C - Long-term effects on HCV-specific and heterologous immune responses (Project Heads Cornberg, Markus ; Wedemeyer, Heiner ; Wölk, Benno )
- A06 - Interaction between hepatitis C virus and lipoproteins and its role for infection and viral persistence (Project Head Pietschmann, Thomas )
- A07 - Mycobacterial adaptation to environmental changes during chronic infection (Project Head Bange, Franz-Christoph )
- A08 - Host and bacterial factors driving chronic Salmonella infections (Project Head Graßl, Guntram Alexander )
- B01 - Visualisation of herpes virus infections and immune responses as well as their modulation (Project Heads Förster, Reinhold ; Messerle, Martin )
- B02 - Immune mediators of cytomegalovirus latency (Project Heads Cicin-Sain, Luka ; Hauser, Hansjörg ; Kalinke, Ulrich )
- B03 - Modulation of the immune response by the gammaherpesviruses Kaposi's sarcoma-associated herpesvirus and murine herpesvirus 68 (Project Heads Brinkmann, Melanie ; Halle, Ph.D., Stephan )
- B04 - Development and Maintenance of T-Cell Immunity during HSV Invasion and Latency (Project Head Behrens, Georg )
- B05 - Evolution of the Hepatitis C Virus (HCV)-specific T-Cell Receptor Repertoire in the Context of Heterologous Immunity: Implications for the Course of an Acute HCV Infection and HCV Vaccine Development (Project Head Cornberg, Markus )
- B06 - Novel host modulatory factors of Helicobacter species (Project Head Josenhans, Christine )
- B07 - Understanding innate and regulatory immune mechanisms against mycobacteria to optimize vaccine strategies (Project Head Sparwasser, Tim Dominik )
- B08 - Towards the use of antigen-specific γδ T lymphocytes for CMV virus control after allogeneic stem cell transplantation (Project Heads Könecke, Christian ; Prinz, Immo )
- B09 - Immune modulation and colonization of sensory ganglia by alphaherpesviruses (Project Head Viejo-Borbolla, Abel )
- B10 - Structural flexibility in the Hepatitis C virus glycoprotein complex as viral strategy to evade the humoral immune system (Project Head Krey, Thomas )
- B11 - The interplay of EBV-induced γδ and αβ T cells during chronic EBV reactivation, PTLD, and EBV-directed cellular therapy in transplant recipients (Project Heads Eiz-Vesper, Britta ; Maecker-Kolhoff, Britta ; Ravens, Sarina )
- C01 - The role of cellular chromatin modulators and DNA repair factors during the establishment and maintenance of gammaherpesvirus latency (Project Head Schulz, Thomas )
- C02 - The establishment of persistent herpes simplex virus infections in ganglia of the peripheral nervous system (Project Head Sodeik, Beate )
- C04 - Impact of the Virus-Producing Cell on HIV Glycosylation and Interaction with Immune cells (Project Heads Gerardy-Schahn, Rita ; Pöhlmann, Stefan )
- C05 - Clinical and Functional Characterization of the Genetic Basis of Chronic Viral Infections in Humans (Project Head Klein, Christoph )
- C06 - Role of cytomegalovirus UL25 protein family members for cell-to-cell spread in persisting infection (Project Head Messerle, Martin )
- C07 - Impact of host variation in the SCARB1 gene and SR-BI ligands on the development and maintenance of chronic hepatitis C (Project Heads Ciesek, Sandra ; Gerold, Gisa ; von Hahn, Thomas )
- C08 - Cellular restriction of HIV-1 by 90K and SERINC5 and their sensitivity to evasion through viral cell-to-cell spread (Project Head Goffinet, Christine )
- Z01 - Central facility for high-throughput sequencing and bioinformatics (Project Heads Prinz, Immo ; Suerbaum, Sebastian ; Tümmler, Burkhard )
- Z02 - Central tasks (Project Head Schulz, Thomas )
Applicant Institution
Medizinische Hochschule Hannover
Participating Institution
Helmholtz-Zentrum für Infektionsforschung (HZI); TWINCORE
Zentrum für Experimentelle und Klinische Infektionsforschung GmbH
Zentrum für Experimentelle und Klinische Infektionsforschung GmbH
Participating University
Ludwig-Maximilians-Universität München; Universität Duisburg-Essen
Spokesperson
Professor Dr. Thomas Schulz