Ectopic expression of a Neospora caninum Kazal type inhibitor triggers developmental defects in Toxoplasma and Plasmodium

Regulated proteolysis is known to control a variety of vital processes in apicomplexan parasites including invasion and egress of host cells. Serine proteases have been proposed as targets for drug development based upon inhibitor studies that show parasite attenuation and transmission blockage. Gen...

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Published in:PloS one Vol. 10; no. 3; p. e0121379
Main Authors: Tampaki, Zoi, Mwakubambanya, Ramadhan S, Goulielmaki, Evi, Kaforou, Sofia, Kim, Kami, Waters, Andrew P, Carruthers, Vern B, Siden-Kiamos, Inga, Loukeris, Thanasis G, Koussis, Konstantinos
Format: Journal Article
Language:English
Published: United States Public Library of Science 24-03-2015
Public Library of Science (PLoS)
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Summary:Regulated proteolysis is known to control a variety of vital processes in apicomplexan parasites including invasion and egress of host cells. Serine proteases have been proposed as targets for drug development based upon inhibitor studies that show parasite attenuation and transmission blockage. Genetic studies suggest that serine proteases, such as subtilisin and rhomboid proteases, are essential but functional studies have proved challenging as active proteases are difficult to express. Proteinaceous Protease Inhibitors (PPIs) provide an alternative way to address the role of serine proteases in apicomplexan biology. To validate such an approach, a Neospora caninum Kazal inhibitor (NcPI-S) was expressed ectopically in two apicomplexan species, Toxoplasma gondii tachyzoites and Plasmodium berghei ookinetes, with the aim to disrupt proteolytic processes taking place within the secretory pathway. NcPI-S negatively affected proliferation of Toxoplasma tachyzoites, while it had no effect on invasion and egress. Expression of the inhibitor in P. berghei zygotes blocked their development into mature and invasive ookinetes. Moreover, ultra-structural studies indicated that expression of NcPI-S interfered with normal formation of micronemes, which was also confirmed by the lack of expression of the micronemal protein SOAP in these parasites. Our results suggest that NcPI-S could be a useful tool to investigate the function of proteases in processes fundamental for parasite survival, contributing to the effort to identify targets for parasite attenuation and transmission blockage.
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Conceived and designed the experiments: TGL K. Kim VC APW. Performed the experiments: ZT RSM EG SK K. Koussis. Analyzed the data: ZT RSM EG K. Koussis ISK TGL. Wrote the paper: ZT RSM K. Koussis K. Kim VC APW ISK TGL.
Current address: Department of Biochemistry and Molecular Biology, Egerton University, P.O. Box 536-20115, Egerton, Kenya
Competing Interests: The authors have declared that no competing interests exist.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0121379