β-1,3-Glucan, Which Can Be Targeted by Drugs, Forms a Trabecular Scaffold in the Oocyst Walls of Toxoplasma and Eimeria

被引:33
作者
Bushkin, G. Guy [1 ,2 ]
Motari, Edwin [1 ]
Magnelli, Paula [1 ]
Gubbels, Marc-Jan [3 ]
Dubey, Jitender P. [4 ]
Miska, Katarzyna B. [4 ]
Bullitt, Esther [5 ]
Costello, Catherine E. [6 ,7 ]
Robbins, Phillips W. [1 ]
Samuelson, John [1 ,2 ]
机构
[1] Boston Univ, Dept Mol & Cell Biol, Goldman Sch Dent Med, Boston, MA 02215 USA
[2] Boston Univ, Dept Microbiol, Sch Med, Boston, MA 02215 USA
[3] Boston Coll, Dept Biol, Chestnut Hill, MA 02167 USA
[4] ARS, Anim Parasit Dis Lab, Anim Nat Resources Inst, USDA, Beltsville, MD USA
[5] Boston Univ, Dept Physiol & Biophys, Sch Med, Boston, MA 02215 USA
[6] Boston Univ, Sch Med, Mass Spectrometry Resource, Boston, MA 02215 USA
[7] Boston Univ, Sch Med, Dept Biochem, Boston, MA 02215 USA
基金
美国农业部; 美国国家卫生研究院;
关键词
CRYPTOSPORIDIUM-PARVUM; GONDII; BRADYZOITES; SPOROZOITES; INFECTIVITY; PROTEINS; BIOLOGY; SURFACE; GENES;
D O I
10.1128/mBio.00258-12
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The walls of infectious pathogens, which are essential for transmission, pathogenesis, and diagnosis, contain sugar polymers that are defining structural features, e. g., beta-1,3-glucan and chitin in fungi, chitin in Entamoeba cysts, beta-1,3-GalNAc in Giardia cysts, and peptidoglycans in bacteria. The goal here was to determine in which of three walled forms of Toxoplasma gondii (oocyst, sporocyst, or tissue cyst) is beta-1,3-glucan, the product of glucan synthases and glucan hydrolases predicted by whole-genome sequences of the parasite. The three most important discoveries were as follows. (i) beta-1,3-glucan is present in oocyst walls of Toxoplasma and Eimeria (a chicken parasite that is a model for intestinal stages of Toxoplasma) but is absent from sporocyst and tissue cyst walls. (ii) Fibrils of beta-1,3-glucan are part of a trabecular scaffold in the inner layer of the oocyst wall, which also includes a glucan hydrolase that has a novel glucan-binding domain. (iii) Echinocandins, which target the glucan synthase and kill fungi, arrest development of the Eimeria oocyst wall and prevent release of the parasites into the intestinal lumen. In summary, beta-1,3-glucan, which can be targeted by drugs, is an important component of oocyst walls of Toxoplasma but is not a component of sporocyst and tissue cyst walls. IMPORTANCE We show here that walls of Toxoplasma oocysts, the infectious stage shed by cats, contain beta-1,3-glucan, a sugar polymer that is a major component of fungal walls. In contrast to fungi, beta-1,3-glucan is part of a trabecular scaffold in the inner layer of the oocyst wall that is independent of the permeability barrier formed by the outer layer of the wall. While glucan synthase inhibitors kill fungi, these inhibitors arrest the development of the oocyst walls of Eimeria (an important chicken pathogen that is a surrogate for Toxoplasma) and block release of oocysts into the intestinal lumen. The absence of beta-1,3-glucan in tissue cysts of Toxoplasma suggests that drugs targeted at the glucan synthase might be used to treat Eimeria in chickens but not to treat Toxoplasma in people.
引用
收藏
页数:9
相关论文
共 33 条
[1]   ApiDB: integrated resources for the apicomplexan bioinformatics resource center [J].
Aurrecoechea, Cristina ;
Heiges, Mark ;
Wang, Haiming ;
Wang, Zhiming ;
Fischer, Steve ;
Rhodes, Philippa ;
Miller, John ;
Kraemer, Eileen ;
Stoeckert, Christian J., Jr. ;
Roos, David S. ;
Kissinger, Jessica C. .
NUCLEIC ACIDS RESEARCH, 2007, 35 :D427-D430
[2]  
Austin Brian R., 2009, V498, P157, DOI 10.1007/978-1-59745-196-3_11
[3]   The coccidian oocyst: a tough nut to crack! [J].
Belli, Sabina I. ;
Smith, Nicholas C. ;
Ferguson, David J. P. .
TRENDS IN PARASITOLOGY, 2006, 22 (09) :416-423
[4]   EmaxDB: Availability of a first draft genome sequence for the apicomplexan Eimeria maxima [J].
Blake, Darner P. ;
Alias, Halimah ;
Billington, Karen J. ;
Clark, Emily L. ;
Mat-Isa, Mohd-Noor ;
Mohamad, Ahmad-Fuad-Hilmi ;
Mohd-Amin, Mohd-Rashdi ;
Tay, Yea-Ling ;
Smith, Adrian L. ;
Tomley, Fiona M. ;
Wan, Kiew-Lian .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 2012, 184 (01) :48-51
[5]   Toxoplasma gondii: 25 years and 25 major advances for the field [J].
Boothroyd, John C. .
INTERNATIONAL JOURNAL FOR PARASITOLOGY, 2009, 39 (08) :935-946
[6]   Suggestive Evidence for Darwinian Selection against Asparagine-Linked Glycans of Plasmodium falciparum and Toxoplasma gondii [J].
Bushkin, G. Guy ;
Ratner, Daniel M. ;
Cui, Jike ;
Banerjee, Sulagna ;
Duraisingh, Manoj T. ;
Jennings, Cameron V. ;
Dvorin, Jeffrey D. ;
Gubbels, Marc-Jan ;
Robertson, Seth D. ;
Steffen, Martin ;
O'Keefe, Barry R. ;
Robbins, Phillips W. ;
Samuelson, John .
EUKARYOTIC CELL, 2010, 9 (02) :228-241
[7]   Forty years of monensin for the control of coccidiosis in poultry [J].
Chapman, H. D. ;
Jeffers, T. K. ;
Williams, R. B. .
POULTRY SCIENCE, 2010, 89 (09) :1788-1801
[8]   Evidence for Mucin-Like Glycoproteins That Tether Sporozoites of Cryptosporidium parvum to the Inner Surface of the Oocyst Wall [J].
Chatterjee, Anirban ;
Banerjee, Sulagna ;
Steffen, Martin ;
O'Connor, Roberta M. ;
Ward, Honorine D. ;
Robbins, Phillips W. ;
Samuelson, John .
EUKARYOTIC CELL, 2010, 9 (01) :84-96
[9]   Innate Recognition of Cell Wall β-Glucans Drives Invariant Natural Killer T Cell Responses against Fungi [J].
Cohen, Nadia R. ;
Tatituri, Raju V. V. ;
Rivera, Amariliz ;
Watts, Gerald F. M. ;
Kim, Edy Y. ;
Chiba, Asako ;
Fuchs, Beth B. ;
Mylonakis, Eleftherios ;
Besra, Gurdyal S. ;
Levitz, Stuart M. ;
Brigl, Manfred ;
Brenner, Michael B. .
CELL HOST & MICROBE, 2011, 10 (05) :437-450
[10]   Gene knock-outs and allelic replacements in Toxoplasma gondii:: HXGPRT as a selectable marker for hit-and-run mutagenesis [J].
Donald, RGK ;
Roos, DS .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1998, 91 (02) :295-305