Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.
Recent Expansion of Toxoplasma Through Enhanced Oral Transmission
C. Su,1*D. Evans,2*R. H. Cole,1J. C. Kissinger,3J. W. Ajioka,2L. D. Sibley1
The global predominance of three clonal
Toxoplasma gondii lineages suggests that they are endowed
with an exceptional traitresponsible for their current parasitism of
nearly all warm-bloodedvertebrates. Genetic polymorphism analyses
indicate that theseclonal lineages emerged within the last 10,000 years after a singlegenetic cross. Comparison with ancient strains
(~1 million years)suggests that the success of the clonal lineages
resulted fromthe concurrent acquisition of direct oral infectivity.
This keyadaptation circumvented sexual recombination, simultaneously
promotingtransmission through successive hosts, hence leading to
clonalexpansion. Thus, changes in complex life cycles can occur
rapidlyand can profoundly influence pathogenicity.
1 Department of Molecular Microbiology,
Washington University, St. Louis, MO 63110, USA.
2 Department of Pathology, Cambridge University,
Cambridge, CB2 1QP, UK.
3 Department of Genetics and
Center for Tropical and Emerging Global Diseases, University of
Georgia, Athens, GA 30602, USA.
*
These authors contributed equally to this work.
To whom correspondence should be addressed. E-mail:
sibley{at}borcim.wustl.edu
The editors suggest the following Related Resources on Science sites:
In Science Magazine
PERSPECTIVES
Sarah K. Volkman and Daniel L. Hartl (17 January 2003) Science299 (5605), 353.
[DOI: 10.1126/science.1081278] |Summary »|Full Text »|PDF »
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
Highly Polymorphic Family of Glycosylphosphatidylinositol-Anchored Surface Antigens with Evidence of Developmental Regulation in Toxoplasma gondii.
A. M. Pollard, K. N. Onatolu, L. Hiller, K. Haldar, and L. J. Knoll (2008)
Infect. Immun.
76, 103-110
|Abstract »|Full Text »|PDF »
Phosphoinositide-3-Kinase-Dependent, MyD88-Independent Induction of CC-Type Chemokines Characterizes the Macrophage Response to Toxoplasma gondii Strains with High Virulence.
C. W. Lee, W. Sukhumavasi, and E. Y. Denkers (2007)
Infect. Immun.
75, 5788-5797
|Abstract »|Full Text »|PDF »
Drugs Designed To Inhibit Human p38 Mitogen-Activated Protein Kinase Activation Treat Toxoplasma gondii and Encephalitozoon cuniculi Infection.
S. Wei, B. J. Daniel, M. J. Brumlik, M. E. Burow, W. Zou, I. A. Khan, S. Wadsworth, J. Siekierka, and T. J. Curiel (2007)
Antimicrob. Agents Chemother.
51, 4324-4328
|Abstract »|Full Text »|PDF »
Recent transcontinental sweep of Toxoplasma gondii driven by a single monomorphic chromosome.
A. Khan, B. Fux, C. Su, J. P. Dubey, M. L. Darde, J. W. Ajioka, B. M. Rosenthal, and L. D. Sibley (2007)
PNAS
104, 14872-14877
|Abstract »|Full Text »|PDF »
Toxoplasma gondii Strains Defective in Oral Transmission Are Also Defective in Developmental Stage Differentiation.
B. Fux, J. Nawas, A. Khan, D. B. Gill, C. Su, and L. D. Sibley (2007)
Infect. Immun.
75, 2580-2590
|Abstract »|Full Text »|PDF »
The MAT1 Locus of Histoplasma capsulatum Is Responsive in a Mating Type-Specific Manner.
A Secreted Serine-Threonine Kinase Determines Virulence in the Eukaryotic Pathogen Toxoplasma gondii.
S. Taylor, A. Barragan, C. Su, B. Fux, S. J. Fentress, K. Tang, W. L. Beatty, H. E. Hajj, M. Jerome, M. S. Behnke, et al. (2006)
Science
314, 1776-1780
|Abstract »|Full Text »|PDF »
Polymorphic Secreted Kinases Are Key Virulence Factors in Toxoplasmosis.
J. P. J. Saeij, J. P. Boyle, S. Coller, S. Taylor, L. D. Sibley, E. T. Brooke-Powell, J. W. Ajioka, and J. C. Boothroyd (2006)
Science
314, 1780-1783
|Abstract »|Full Text »|PDF »
Common inheritance of chromosome Ia associated with clonal expansion of Toxoplasma gondii.
A. Khan, U. Bohme, K. A. Kelly, E. Adlem, K. Brooks, M. Simmonds, K. Mungall, M. A. Quail, C. Arrowsmith, T. Chillingworth, et al. (2006)
Genome Res.
16, 1119-1125
|Abstract »|Full Text »|PDF »
Toxoplasma gondii Genotype Determines MyD88-Dependent Signaling in Infected Macrophages.
L. Kim, B. A. Butcher, C. W. Lee, S. Uematsu, S. Akira, and E. Y. Denkers (2006)
J. Immunol.
177, 2584-2591
|Abstract »|Full Text »|PDF »
From the Cover: Globalization and the population structure of Toxoplasma gondii.
T. Lehmann, P. L. Marcet, D. H. Graham, E. R. Dahl, and J. P. Dubey (2006)
PNAS
103, 11423-11428
|Abstract »|Full Text »|PDF »
Just one cross appears capable of dramatically altering the population biology of a eukaryotic pathogen like Toxoplasma gondii.
J. P. Boyle, B. Rajasekar, J. P. J. Saeij, J. W. Ajioka, M. Berriman, I. Paulsen, D. S. Roos, L. D. Sibley, M. W. White, and J. C. Boothroyd (2006)
PNAS
103, 10514-10519
|Abstract »|Full Text »|PDF »
Genotyping of Toxoplasma gondii by Multiplex PCR and Peptide-Based Serological Testing of Samples from Infants in Poland Diagnosed with Congenital Toxoplasmosis.
D. Nowakowska, I. Colon, J. S. Remington, M. Grigg, E. Golab, J. Wilczynski, and L. D. Sibley (2006)
J. Clin. Microbiol.
44, 1382-1389
|Abstract »|Full Text »|PDF »
Pair of Unusual GCN5 Histone Acetyltransferases and ADA2 Homologues in the Protozoan Parasite Toxoplasma gondii.
M. M. Bhatti, M. Livingston, N. Mullapudi, and W. J. Sullivan Jr. (2006)
Eukaryot. Cell
5, 62-76
|Abstract »|Full Text »|PDF »
Genotyping of Toxoplasma gondii Strains from Immunocompromised Patients Reveals High Prevalence of Type I Strains.
A. Khan, C. Su, M. German, G. A. Storch, D. B. Clifford, and L. D. Sibley (2005)
J. Clin. Microbiol.
43, 5881-5887
|Abstract »|Full Text »|PDF »
Clinical and Environmental Isolates of Cryptococcus gattii from Australia That Retain Sexual Fecundity.
L. T. Campbell, J. A. Fraser, C. B. Nichols, F. S. Dietrich, D. Carter, and J. Heitman (2005)
Eukaryot. Cell
4, 1410-1419
|Abstract »|Full Text »|PDF »
Composite genome map and recombination parameters derived from three archetypal lineages of Toxoplasma gondii.
A. Khan, S. Taylor, C. Su, A. J. Mackey, J. Boyle, R. Cole, D. Glover, K. Tang, I. T. Paulsen, M. Berriman, et al. (2005)
Nucleic Acids Res.
33, 2980-2992
|Abstract »|Full Text »|PDF »
Multiplex PCR for Typing Strains of Toxoplasma gondii.
D. Ajzenberg, A. Dumetre, and M.-L. Darde (2005)
J. Clin. Microbiol.
43, 1940-1943
|Abstract »|Full Text »|PDF »
Bioluminescence Imaging of Toxoplasma gondii Infection in Living Mice Reveals Dramatic Differences between Strains.
J. P. J. Saeij, J. P. Boyle, M. E. Grigg, G. Arrizabalaga, and J. C. Boothroyd (2005)
Infect. Immun.
73, 695-702
|Abstract »|Full Text »|PDF »
The unpredictable past of Plasmodium vivax revealed in its genome.
Subpopulation Characteristics of Egg-Contaminating Salmonella enterica serovar Enteritidis as Defined by the Lipopolysaccharide O Chain.
J. Guard-Bouldin, R. K. Gast, T. J. Humphrey, D. J. Henzler, C. Morales, and K. Coles (2004)
Appl. Envir. Microbiol.
70, 2756-2763
|Abstract »|Full Text »|PDF »
Recapitulation of the Sexual Cycle of the Primary Fungal Pathogen Cryptococcus neoformans var. gattii: Implications for an Outbreak on Vancouver Island, Canada.
J. A. Fraser, R. L. Subaran, C. B. Nichols, and J. Heitman (2003)
Eukaryot. Cell
2, 1036-1045
|Abstract »|Full Text »|PDF »
Sexual Cycle of Cryptococcus neoformans var. grubii and Virulence of Congenic a and {alpha} Isolates.
K. Nielsen, G. M. Cox, P. Wang, D. L. Toffaletti, J. R. Perfect, and J. Heitman (2003)
Infect. Immun.
71, 4831-4841
|Abstract »|Full Text »|PDF »
No Sex a Key to Success for Toxoplasma.
(2003)
Journal Watch Infectious Diseases
2003, 13
|Full Text »