4.6 Article

Neospora caninum: Differential Proteome of Multinucleated Complexes Induced by the Bumped Kinase Inhibitor BKI-1294

Journal

MICROORGANISMS
Volume 8, Issue 6, Pages -

Publisher

MDPI
DOI: 10.3390/microorganisms8060801

Keywords

antigenic variation; chemotherapy; drug adaptation; drug resistance

Categories

Funding

  1. Swiss National Science Foundation [310030_184662]
  2. National Institutes of Health (NIH) [R01AI089441, R01AI111341, R21AI123690, R21AI140881]
  3. Swiss National Science Foundation (SNF) [310030_184662] Funding Source: Swiss National Science Foundation (SNF)

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Background: the apicomplexan parasiteNeospora caninumcauses important reproductive problems in farm animals, most notably in cattle. After infection via oocysts or tissue cysts, rapidly dividing tachyzoites infect various tissues and organs, and in immunocompetent hosts, they differentiate into slowly dividing bradyzoites, which form tissue cysts and constitute a resting stage persisting within infected tissues. Bumped kinase inhibitors (BKIs) of calcium dependent protein kinase 1 are promising drug candidates for the treatment ofNeosporainfections. BKI-1294 exposure of cell cultures infected withN. caninumtachyzoites results in the formation of massive multinucleated complexes (MNCs) containing numerous newly formed zoites, which remain viable for extended periods of time under drug pressure in vitro. MNC and tachyzoites exhibit considerable antigenic and structural differences. Methods: Using shotgun mass spectrometry, we compared the proteomes of tachyzoites to BKI-1294 induced MNCs, and analyzed the mRNA expression levels of selected genes in both stages. Results: More than half of the identified proteins are downregulated in MNCs as compared to tachyzoites. Only 12 proteins are upregulated, the majority of them containing SAG1 related sequence (SRS) domains, and some also known to be expressed in bradyzoites Conclusions: MNCs exhibit a proteome different from tachyzoites, share some bradyzoite-like features, but may constitute a third stage, which remains viable and ensures survival under adverse conditions such as drug pressure. We propose the term baryzoites for this stage (from Greek beta alpha rho upsilon sigma = massive, bulky, heavy, inert).

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