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Infect Immun, April 1998, p. 1632-1637, Vol. 66, No. 4
0019-9567/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Expressed Sequence Tag Analysis of the
Bradyzoite Stage of Toxoplasma gondii: Identification
of Developmentally Regulated Genes
Ian D.
Manger,1
Adrian
Hehl,1
Steve
Parmley,2
L. David
Sibley,3
Marco
Marra,4
Ladeana
Hillier,4
Robert
Waterston,4 and
John
C.
Boothroyd1,*
Department of Microbiology and Immunology,
Stanford University, Stanford, California
94305-51241;
Department of Immunology,
Palo Alto Medical Foundation, Palo Alto, California
943012; and
Department of Molecular
Microbiology3 and
Department of
Genetics,4 Washington University, St. Louis,
Missouri 63110
Received 3 November 1997/Returned for modification 8 December
1997/Accepted 11 January 1998
Toxoplasma gondii is a protozoan parasite responsible
for widespread infections in humans and animals. Two major asexual
forms are produced during the life cycle of this parasite: the rapidly dividing tachyzoite and the more slowly dividing, encysted bradyzoite. To further study the differentiation between these two forms, we have
generated a large number of expressed sequence tags (ESTs) from both
asexual stages. Previously, we obtained data on ~7,400 ESTs from
tachyzoites (J. Ajioka et al., Genome Res. 8:18-28, 1998). Here, we
report the results from analysis of ~2,500 ESTs from bradyzoites
purified from the cysts of infected mice. We also report the results
from analysis of 760 ESTs from parasites induced to differentiate from
tachyzoites to bradyzoites in vitro. Comparison of the data sets from
bradyzoites and tachyzoites reveals many previously uncharacterized
sequence clusters which are largely or completely specific to one or
other developmental stage. This class includes a bradyzoite-specific
form of enolase. Combined with the previously identified
bradyzoite-specific form of lactate dehydrogenase, this finding
suggests significant differences in flux through the lower end of the
glycolytic pathway in this stage. Thus, the generation of this data set
provides valuable insights into the metabolism and growth of the
parasite in the encysted form and represents a substantial body of
information for further study of development in Toxoplasma.
*
Corresponding author. Mailing address: Department of
Microbiology and Immunology, Sherman Fairchild Science Building, 300 Pasteur Dr., Stanford, CA 94305-5124. Phone: (650) 723-7984. Fax: (650)
723-6853. E-mail: john.boothroyd{at}stanford.edu.
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