Abstract
Eimeria ninakohlyakimovae is an important coccidian parasite of goats which causes severe diarrhoea in young animals. Specific molecules that mediate E. ninakohlyakimovae host interactions and molecular mechanisms involved in the pathogenesis are still unknown. Although strong circumstantial evidence indicates that E. ninakohlyakimovae sporozoite interactions with caprine endothelial host cells (ECs) are specific, hardly any information is available about the interacting molecules that confer host cell specificity. In this study, we describe a novel method to identify surface proteins of caprine umbilical vein endothelial cells (CUVEC) using a phage display library. After several panning rounds, we identified a number of peptides that specifically bind to the surface of CUVEC. Importantly, caprine endothelial cell peptide 2 (PCEC2) and PCEC5 selectively reduced the infection rate by E. ninakohlyakimovae sporozoites. These preliminary data give new insight for the molecular identification of ligands involved in the interaction between E. ninakohlyakimovae sporozoites and host ECs. Further studies using this phage approach might be useful to identify new potential target molecules for the development of anti-coccidial drugs or even new vaccine strategies.

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Acknowledgments
This study was funded by the Spanish Ministry of Science and Innovation (MICIN, project nr. AGL2007-63415) and FEDER funds of the European Community. The Canary Agency of Investigation, Innovation and Society of Information (ACIISI, project SolSubc2200801000244) is also here acknowledged for their financial support. This project received financial support from the National Institute of Allergy and Infectious Diseases (grant R01 AI031478 to MJL).
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Ruiz, A., Pérez, D., Muñoz, M.C. et al. Targeting essential Eimeria ninakohlyakimovae sporozoite ligands for caprine host endothelial cell invasion with a phage display peptide library. Parasitol Res 114, 4327–4331 (2015). https://doi.org/10.1007/s00436-015-4666-x
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DOI: https://doi.org/10.1007/s00436-015-4666-x