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  3. Recruitment of EB1, a master regulator of microtubule dynamics, to the surface of the Theileria annulata schizont

Recruitment of EB1, a master regulator of microtubule dynamics, to the surface of the Theileria annulata schizont

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DOI
10.7892/boris.43932
Publisher DOI
10.1371/journal.ppat.1003346
PubMed ID
23675298
Abstract
The apicomplexan parasite Theileria annulata transforms infected host cells, inducing uncontrolled proliferation and clonal expansion of the parasitized cell population. Shortly after sporozoite entry into the target cell, the surrounding host cell membrane is dissolved and an array of host cell microtubules (MTs) surrounds the parasite, which develops into the transforming schizont. The latter does not egress to invade and transform other cells. Instead, it remains tethered to host cell MTs and, during mitosis and cytokinesis, engages the cell's astral and central spindle MTs to secure its distribution between the two daughter cells. The molecular mechanism by which the schizont recruits and stabilizes host cell MTs is not known. MT minus ends are mostly anchored in the MT organizing center, while the plus ends explore the cellular space, switching constantly between phases of growth and shrinkage (called dynamic instability). Assuming the plus ends of growing MTs provide the first point of contact with the parasite, we focused on the complex protein machinery associated with these structures. We now report how the schizont recruits end-binding protein 1 (EB1), a central component of the MT plus end protein interaction network and key regulator of host cell MT dynamics. Using a range of in vitro experiments, we demonstrate that T. annulata p104, a polymorphic antigen expressed on the schizont surface, functions as a genuine EB1-binding protein and can recruit EB1 in the absence of any other parasite proteins. Binding strictly depends on a consensus SxIP motif located in a highly disordered C-terminal region of p104. We further show that parasite interaction with host cell EB1 is cell cycle regulated. This is the first description of a pathogen-encoded protein to interact with EB1 via a bona-fide SxIP motif. Our findings provide important new insight into the mode of interaction between Theileria and the host cell cytoskeleton.
Date Issued
2013-05
Publication Type
Article
Language(s)
en
Author(s)
Woods, Kerry  
Department of Clinical Research and Veterinary Public Health, Molekulare Pathobiologie  
Theiler, Romina  
Department of Clinical Research and Veterinary Public Health, Molekulare Pathobiologie  
Mühlemann, Markus  
Department of Clinical Research and Veterinary Public Health, Molekulare Pathobiologie  
Segiser, Adrian  
Department of Clinical Research and Veterinary Public Health, Molekulare Pathobiologie  
Huber, Sandra  
Department of Clinical Research and Veterinary Public Health, Molekulare Pathobiologie  
Ansari, Hifzur R.
Pain, Arnab
Dobbelaere, Dirk,  
Department of Clinical Research and Veterinary Public Health, Molekulare Pathobiologie  
Additional Credits
Department of Clinical Research and Veterinary Public Health, Molekulare Pathobiologie  
Journal
PLoS pathogens
Publisher
Public Library of Science
ISSN
1553-7366
Access(Rights)
open.access
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