Electrophoresis. 2013 Oct 24. doi: 10.1002/elps.201300044. [Epub ahead of print]
Comparative proteomic analysis of different Toxoplasma gondii genotypes by two-dimensional fluorescence difference gel electrophoresis combined with mass spectrometry
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State Key Laboratory of Veterinary Etiological Biology, Key Laboratory of Veterinary Parasitology of Gansu Province, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, Gansu Province, 730046, China.Abstract
Toxoplasma gondii is a protozoan parasite infecting almost all warm-blooded animals and humans. There are three infective stages of T. gondii: the tachyzoites, the bradyzoites and the oocysts. The tachyzoite is a rapidly multiplying stage and the main pathogenic factor. In North America and Europe, T. gondii is consisted of four major clonal lineages (namely Types I, II, III and Type 12). In this study, we explored the proteomic profiles of different genotypes (Type I-RH strain, Type II-PRU strain, Type II-TgQHO strain and ToxoDB 9-TgC7 strain) of T. gondii tachyzoites by using two-dimensional fluorescence difference gel electrophoresis (2D DIGE) combined with MALDI-TOF MS. Totally, 110 differentially abundant protein spots were selected. Of these, 98 spots corresponding to 56 proteins from T. gondii were successfully identified. These included surface antigen (SAG1), heat shock protein 70 (Hsp70), disulfide isomerase, coronin, heat shock protein 60 (Hsp60), pyruvate kinase, receptor for activated C kinase 1 and peroxiredoxin. Gene ontology (GO) enrichment analysis revealed that most of the differentially abundant proteins were involved in biological regulation, metabolic process, response to stress, binding, antioxidant activity and transporter activity. According to the Kyoto Encyclopedia of Genes and Genomes (KEGG) metabolic pathway maps of T. gondii, some identified proteins were involved in the glycolytic/gluconeogenesis pathway. The present study identified differentially abundant proteins among different genotypes of T. gondii and these findings have implications for the better understanding of the phenotypic differences among the examined T. gondii genotypes which in turn may contribute to the better control of toxoplasmosis. This article is protected by copyright. All rights reserved.
This article is protected by copyright. All rights reserved.
This article is protected by copyright. All rights reserved.
KEYWORDS:
2D DIGE, Mass spectrometry, Proteome, Tachyzoites, Toxoplasma gondii- PMID:
- 24166805
- [PubMed - as supplied by publisher]
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