Resistance towards monensin is proposed to be acquired in aToxoplasma gondiimodel by reduced invasion and egress activities, in addition to increased intracellular replication

Male Proteomics Cytoplasm 0303 health sciences Proteome Foreskin Drug Resistance Protozoan Proteins Toxoplasma gondii Computational Biology Fibroblasts SILAC Actins Host-Parasite Interactions monensin 03 medical and health sciences Tandem Mass Spectrometry Coccidiostats Humans stable isotope labelling by amino acid in cell culture Monensin Toxoplasma resistance mechanism Chromatography, Liquid
DOI: 10.1017/s0031182017001512 Publication Date: 2017-09-05T05:11:23Z
ABSTRACT
SUMMARYMonensin (Mon) is an anticoccidial polyether ionophore widely used to control coccidiosis. The extensive use of polyether ionophores on poultry farms resulted in widespread resistance, but the underlying resistance mechanisms are unknown in detail. For analysing the mode of action by which resistance against polyether ionophores is obtained, we inducedin vitroMon resistance inToxoplasma gondii-RH strain (MonR-RH) and compared it with the sensitive parental strain (Sen-RH). The proteome assessment of MonR-RH and Sen-RH strains was obtained after isotopic labelling using stable isotope labelling by amino acid in cell culture. Relative proteomic quantification between resistant and sensitive strains was performed using liquid chromatography-mass spectrometry/mass spectrometry. Overall, 1024 proteins were quantified and 52 proteins of them were regulated. The bioinformatic analysis revealed regulation of cytoskeletal and transmembrane proteins being involved in transport mechanisms, metal ion-binding and invasion. During invasion, actin and microneme protein 8 (MIC8) are seem to be important for conoid extrusion and forming moving junction with host cells, respectively. Actin was significantly upregulated, while MIC8 was downregulated, which indicate an invasion reduction in the resistant strain. Resistance against Mon is not a simple process but it involves reduced invasion and egress activity ofT. gondiitachyzoites while intracellular replication is enhanced.
SUPPLEMENTAL MATERIAL
Coming soon ....
REFERENCES (51)
CITATIONS (8)