Abstract
BackgroundA global proteomic strategy was used to identify proteins, which are differentially expressed in the murine model of severe malaria in the hope of facilitating future development of novel diagnostic, disease monitoring and treatment strategies.MethodsMice (4-week-old CD1 male mice) were infected with Plasmodium berghei ANKA strain, and infection allowed to establish until a parasitaemia of 30% was attained. Total plasma and albumin depleted plasma samples from infected and control (non-infected) mice were separated by two-dimensional gel electrophoresis (2-DE). After staining, the gels were imaged and differential protein expression patterns were interrogated using image analysis software. Spots of interest were then digested using trypsin and the proteins identified using matrix-assisted laser desorption and ionization-time of flight (MALDI-TOF) mass spectrometry (MS) and peptide mass fingerprinting software.ResultsMaster gels of control and infected mice, and the corresponding albumin depleted fractions exhibited distinctly different 2D patterns comparing control and infected plasma, respectively. A wide range of proteins demonstrated altered expression including; acute inflammatory proteins, transporters, binding proteins, protease inhibitors, enzymes, cytokines, hormones, and channel/receptor-derived proteins.ConclusionsMalaria-infection in mice results in a wide perturbation of the host serum proteome involving a range of proteins and functions. Of particular interest is the increased secretion of anti-inflammatory and anti apoptotic proteins.
Highlights
A global proteomic strategy was used to identify proteins, which are differentially expressed in the murine model of severe malaria in the hope of facilitating future development of novel diagnostic, disease monitoring and treatment strategies
Cerebral malaria is induced in susceptible strains of mice by the ANKA strain of Plasmodium berghei [2]
These murine models of cerebral malaria have been used in the past to throw light on the pathogenesis of the human condition [3,4,5,6]
Summary
A global proteomic strategy was used to identify proteins, which are differentially expressed in the murine model of severe malaria in the hope of facilitating future development of novel diagnostic, disease monitoring and treatment strategies. Animal models of cerebral malaria have been developed to provide insight in to the pathogenesis of the disease it is accepted that there are differences from the human condition. Cerebral malaria is induced in susceptible strains of mice by the ANKA strain of Plasmodium berghei [2]. These murine models of cerebral malaria have been used in the past to throw light on the pathogenesis of the human condition [3,4,5,6]. Proteomic studies characterize the complex network of cell regulation at the protein level
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