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  Hervé Agaisse
Assistant Professor
Microbial Pathogenesis
Ph.D. Pasteur Institute 1996
e-mail: herve.agaisse@yale.edu
phone: (203) 737-2404


Research Interests

Multicellular organisms are continuously exposed to pathogenic microorganisms and have evolved sophisticated mechanisms that protect them from infection. Over the past decade, a fascinating notion has emerged: the mechanisms involved in innate immunity have been conserved throughout evolution. Taking advantage of this situation, we are using Drosophila melanogaster as a genetic system to investigate biological processes related to the mammalian innate immune response.

In a first aspect of our research program, we use the power of Drosophila genetics to investigate how various aspects of the immune response are integrated at the level of an organism. In particular, we study the role of Drosophila blood cells in the response to stressful conditions. Our main focus is to understand how blood cells detect stressful events and subsequently convey this information to immune organs through the production of signaling molecules. Altogether, our genetic approach in Drosophila will potentially lead to the identification of uncovered signaling components that may be relevant to the immune response in mammals.

In a second aspect of our research program, we use Drosophila cell lines to model the development of human intracellular pathogens. We have recently completed a full-genome RNAi-based screen that led to the identification of host factors involved in the development of Listeria, a human cytosolic intracellular pathogen. We are now conducting similar screens with intracellular pathogens displaying a similar or a different life style, such as Shigella and Chlamydia. Importantly, we use siRNA-based gene expression silencing methodologies to test in a mammalian system the functional relevance of the identified host factors.

Selected References

Agaisse, H., Burrack, L., Philips, J., Perrimon N. and Darren Higgins D. Genome-wide RNAi screen for host factors required for intracellular bacterial infection. Science. 2005. 309(5738):1248-51. PDF

Agaisse, H. and Perrimon, N. 2004. Roles of JAK/STAT signaling in Drosophila immune response. Immunol Rev. 2004. 198:72-82. PDF

Agaisse, H., Petersen, U-M., Boutros, M., Mathey-Prevot, B. and Perrimon, N. 2003. Signaling role of hemocytes in Drosophila JAK/STAT-dependent response to septic injury. Dev Cell 5(3):441-450. PDF

Boutros, M., Agaisse H., Perrimon N. 2002. Sequential activation of signaling pathways during innate immune responses in Drosophila. Dev Cell. 3(5):711-22. PDF


Yale University
School of Medicine
Boyer Center for
Molecular Medicine
Section of Microbial
Pathogenesis
295 Congress Ave.
New Haven, CT
06536-0812 USA
 
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Yale School of Medicine, Section of Microbial Pathogenesis.
Phone (203) 737-2404, FAX (203) 737-2630.