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Philippe Hauser Lab

Philippe Hauser, PhD, MER
++41 (0)21 314 4084
++41 (0)79 556 2298
philippe.hauser@chuv.ch

Research topics

Search for new therapeutic target against Pneumocystis jirovecii

In the absence of efficient therapy to replace antifolates, we look for new therapeutic targets. We investigate enzymes involved in the biosynthesis of folates which were not previously used as targets, as well as genes which function is still unknown. The function of the latter is determined by their expression in model yeasts (Saccharomyces cerevisiae, Schizosaccharomyces pombe).

Epidemiology of Pneumocystis jirovecii

Pneumocystis jirovecii is a microscopic fungus causing severe pneumonia in immuno-compromised patients (transplantation, leukemia, AIDS, etc.). In the absence of an in vitro culture system, the biology of this fungus remains poorly known which prevents efficient fight against this pathogen.
In order to improve prevention measures for patients at high risk, we are searching the sources of the infection. We showed that patients with active Pneumocystis pneumonia are a potential source. We investigate if certain categories of persons may carry Pneumocystis without any symptoms and constitute an important source of the disease.

Resistance of Pneumocystis jirovecii to antifolates

Antifolates are the most efficient drugs for the prophylaxis and treatment of Pneumocystis pneumonia. Their use is nevertheless correlated with the appearance of mutations in their target genes. We study the resistance conferred by the mutations observed in strains isolated from patients. We also study the possibility that other mechanisms of resistance are involved using the model organism Saccharomyces cerevisiae.

Current lab members
Name Position Contact
Ousmane Cissé Doctorant ousmane.cisse@chuv.ch
Sophie Chevalley Technician sophie.chevalley@chuv.ch

Selected publications


2010

1: Gianella S, Haeberli L, Joos B, Ledergerber B, Wüthrich RP, Weber R, Kuster H, Hauser PM, Fehr T, Mueller NJ.
    Molecular evidence of interhuman transmission in an outbreak of Pneumocystis jirovecii pneumonia among renal transplant recipients.
Transpl Infect Dis. 2010 Feb;12(1):1-10.
2: Hauser PM, Nahimana A, Taffe P, Weber R, Francioli P, Bille J, Rabodonirina M.
    Interhuman transmission as a potential key parameter for geographical variation in the prevalence of Pneumocystis jirovecii dihydropteroate synthase mutations.
Clin Infect Dis. 2010 Aug 15;51(4):e28-33.

2009

1: Cockell MM, Lo Presti L, Cerutti L, Cano Del Rosario E, Hauser PM, Simanis V.
    Functional differentiation of tbf1 orthologues in fission and budding yeasts.
Eukaryot Cell. 2009 Feb;8(2):207-16.
2: Lo Presti L, Cerutti L, Monod M, Hauser PM.
    Choice of an adequate promoter for efficient complementation in Saccharomyces cerevisiae: a case study.
Res Microbiol. 2009 Jul-Aug;160(6):380-8.

2008

1: Nevez G, Chabé M, Rabodonirina M, Virmaux M, Dei-Cas E, Hauser PM, Totet A.
    Nosocomial Pneumocystis jirovecii infections.
Parasite. 2008 Sep;15(3):359-65.

2007

1: Lo Presti L, Cockell M, Cerutti L, Simanis V, Hauser PM.
    Functional Characterization of Pneumocystis carinii brl1 by Transspecies Complementation Analysis.
Eukaryot Cell. 2007 Dec;6(12):2448-52. Epub 2007 Nov 9.

2006

1: Hauser PM, Macreadie IG
    Isolation of the Pneumocystis carinii dihydrofolate synthase gene and functional complementation in Saccharomyces cerevisiae.
FEMS Microbiol Lett. 2006 Mar;256(2):244-50

2005

1: Hocker B, Wendt C, Nahimana A, Tonshoff B, Hauser PM
    Molecular evidence of Pneumocystis transmission in pediatric transplant unit
Emerg Infect Dis. 2005 Feb;11(2):330-2.

2004

1: Meneau I, Sanglard D, Bille J, Hauser PM
    Pneumocystis jiroveci dihydropteroate synthase polymorphisms confer resistance to sulfadoxine and sulfanilamide in Saccharomyces cerevisiae.
Antimicrob Agents Chemother. 2004 Jul;48(7):2610-6


Last Update on 24.08.2010 - Publication credits - Legal information

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