Journal article

P-Glycoprotein Inhibitors Differently Affect Toxoplasma gondii, Neospora caninum and Besnoitia besnoiti Proliferation in Bovine Primary Endothelial Cells


Authors listLarrazabal, Camilo; Silva, Liliana M. R.; Pervizaj-Oruqaj, Learta; Herold, Susanne; Hermosilla, Carlos; Taubert, Anja

Publication year2021

JournalPathogens

Volume number10

Issue number4

eISSN2076-0817

Open access statusGold

DOI Linkhttps://doi.org/10.3390/pathogens10040395

PublisherMDPI


Abstract
Apicomplexan parasites are obligatory intracellular protozoa. In the case of Toxoplasma gondii, Neospora caninum or Besnoitia besnoiti, to ensure proper tachyzoite production, they need nutrients and cell building blocks. However, apicomplexans are auxotrophic for cholesterol, which is required for membrane biosynthesis. P-glycoprotein (P-gp) is a transmembrane transporter involved in xenobiotic efflux. However, the physiological role of P-gp in cholesterol metabolism is unclear. Here, we analyzed its impact on parasite proliferation in T. gondii-, N. caninum- and B. besnoiti-infected primary endothelial cells by applying different generations of P-gp inhibitors. Host cell treatment with verapamil and valspodar significantly diminished tachyzoite production in all three parasite species, whereas tariquidar treatment affected proliferation only in B. besnoiti. 3D-holotomographic analyses illustrated impaired meront development driven by valspodar treatment being accompanied by swollen parasitophorous vacuoles in the case of T. gondii. Tachyzoite and host cell pre-treatment with valspodar affected infection rates in all parasites. Flow cytometric analyses revealed verapamil treatment to induce neutral lipid accumulation. The absence of a pronounced anti-parasitic impact of tariquidar, which represents here the most selective P-gp inhibitor, suggests that the observed effects of verapamil and valspodar are associated with mechanisms independent of P-gp. Out of the three species tested here, this compound affected only B. besnoiti proliferation and its effect was much milder as compared to verapamil and valspodar.



Citation Styles

Harvard Citation styleLarrazabal, C., Silva, L., Pervizaj-Oruqaj, L., Herold, S., Hermosilla, C. and Taubert, A. (2021) P-Glycoprotein Inhibitors Differently Affect Toxoplasma gondii, Neospora caninum and Besnoitia besnoiti Proliferation in Bovine Primary Endothelial Cells, Pathogens, 10(4), Article 395. https://doi.org/10.3390/pathogens10040395

APA Citation styleLarrazabal, C., Silva, L., Pervizaj-Oruqaj, L., Herold, S., Hermosilla, C., & Taubert, A. (2021). P-Glycoprotein Inhibitors Differently Affect Toxoplasma gondii, Neospora caninum and Besnoitia besnoiti Proliferation in Bovine Primary Endothelial Cells. Pathogens. 10(4), Article 395. https://doi.org/10.3390/pathogens10040395



Keywords


ABCB1-transporterCELLULAR CHOLESTEROLCHLOROQUINE RESISTANCENeospora caninumSMOOTH-MUSCLE-CELLStariquidarvalspodarVERAPAMIL

Last updated on 2025-10-06 at 11:24