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Infection and Immunity, April 2008, p. 1686-1694, Vol. 76, No. 4
0019-9567/08/$08.00+0     doi:10.1128/IAI.01497-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Combined Inactivation of the Candida albicans GPR1 and TPS2 Genes Results in Avirulence in a Mouse Model for Systemic Infection{triangledown}

Mykola M. Maidan,1,2 Larissa De Rop,1,2 Miguel Relloso,3 Rosalia Diez-Orejas,3 Johan M. Thevelein,1,2 and Patrick Van Dijck1,2*

VIB Department of Molecular Microbiology,1 Laboratory of Molecular Cell Biology, K.U. Leuven, Kasteelpark Arenberg 31, B-3001 Leuven, Belgium,2 Departamento de Microbiología II, Facultad de Farmacia, Universidad Complutense, 28040 Madrid, Spain3

Received 9 November 2007/ Returned for modification 19 December 2007/ Accepted 1 February 2008

Inhibition of the biosynthesis of trehalose, a well-known stress protectant in pathogens, is an interesting approach for antifungal or antibacterial therapy. Deletion of TPS2, encoding trehalose-6-phosphate (T6P) phosphatase, results in strongly reduced virulence of Candida albicans due to accumulation of T6P instead of trehalose in response to stress. To further aggravate the deregulation in the pathogen, we have additionally deleted the GPR1 gene, encoding the nutrient receptor that activates the cyclic AMP-protein kinase A signaling pathway, which negatively regulates trehalose accumulation in yeasts. A gpr1 mutant is strongly affected in morphogenesis on solid media as well as in vivo in a mouse model but has only a slightly decreased virulence. The gpr1 tps2 double mutant, on the other hand, is completely avirulent in a mouse model for systemic infection. This strain accumulates very high T6P levels under stress conditions and has a growth defect at higher temperatures. We also show that a tps2 mutant is more sensitive to being killed by macrophages than the wild type or the gpr1 mutant. A double mutant has susceptibility similar to that of the single tps2 mutant. For morphogenesis on solid media, on the other hand, the gpr1 tps2 mutant shows a phenotype similar to that of the single gpr1 mutant. Taken together these results show that there is synergism between Gpr1 and Tps2 and that their combined inactivation results in complete avirulence. Combination therapy targeting both proteins may prove highly effective against pathogenic fungi with increased resistance to the currently used antifungal drugs.

* Corresponding author. Mailing address: VIB Department of Molecular Microbiology, Laboratory of Molecular Cell Biology, K.U. Leuven, Kasteelpark Arenberg 31, B-3001 Leuven, Belgium. Phone: 32 16321512. Fax: 32 16321979. E-mail: Patrick.vandijck{at}bio.kuleuven.be

{triangledown} Published ahead of print on 11 February 2008.

Editor: A. Casadevall

Infection and Immunity, April 2008, p. 1686-1694, Vol. 76, No. 4
0019-9567/08/$08.00+0     doi:10.1128/IAI.01497-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.





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