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Eukaryotic Cell, October 2003, p. 1053-1060, Vol. 2, No. 5
1535-9778/03/$08.00+0 DOI: 10.1128/EC.2.5.1053-1060.2003
Copyright © 2003, American
Society for
Microbiology. All Rights Reserved.
Engineered Control of Cell Morphology In Vivo Reveals Distinct Roles for Yeast and Filamentous Forms of Candida albicans during Infection
Stephen P. Saville,1* Anna L. Lazzell,1 Carlos Monteagudo,2 and Jose L. Lopez-Ribot1
Division
of Infectious Diseases, Department of Medicine, University of Texas
Health Science Center at San Antonio, San Antonio, Texas
78245,1
Departmento de
Patología, Facultad de Medicina y Odontología,
Universidad de Valencia, 46010 Valencia,
Spain2
Received 24 July 2003/
Accepted 29 July 2003
It
is widely assumed that the ability of Candida albicans to
switch between different morphologies is required for pathogenesis.
However, most virulence studies have used mutants that are permanently
locked into either the yeast or filamentous forms which are avirulent
but unsuitable for discerning the role of morphogenetic conversions at
the various stages of the infectious process. We have constructed a
strain in which this developmental transition can be externally
modulated both in vitro and in vivo. This was achieved by placing one
copy of the NRG1 gene (a negative regulator of filamentation)
under the control of a tetracycline-regulatable promoter. This modified
strain was then tested in an animal model of hematogenously
disseminated candidiasis. Mice injected with this strain under
conditions permitting hyphal development succumbed to the infection,
whereas all of the animals injected under conditions that inhibited
this transition survived. Importantly, fungal burdens were almost
identical in both sets of animals, indicating that, whereas filament
formation appears to be required for the mortality resulting from a
deep-seated infection, yeast cells play an important role early in the
infectious process by extravasating and disseminating to the target
organs. Moreover, these infecting Candida yeast cells still
retained their pathogenic potential, as demonstrated by allowing this
developmental transition to occur at various time points postinfection.
We demonstrate here the importance of morphogenetic conversions in
C. albicans pathogenesis. This engineered strain should
provide a useful tool in unraveling the individual contributions of the
yeast and filamentous forms at various stages of the infectious
process.
* Corresponding
author. Mailing address: Division of Infectious Diseases, Department of
Medicine, University of Texas Health Science Center at San Antonio,
STCBM, 15355 Lambda Dr., San Antonio, TX 78245. Phone: (210) 562-5018.
Fax: (210) 562-5016. E-mail:
saville{at}uthscsa.edu.
Eukaryotic Cell, October 2003, p. 1053-1060, Vol. 2, No. 5
1535-9778/03/$08.00+0 DOI: 10.1128/EC.2.5.1053-1060.2003
Copyright © 2003, American
Society for
Microbiology. All Rights Reserved.
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