Centre for Biodiscovery and School of Biological Sciences, Victoria University of Wellington, Wellington, 6140 New Zealand.
J Proteomics. 2012 Mar 16;75(6):1838-48. doi: 10.1016/j.jprot.2011.12.025. Epub 2012 Jan 10.
Chronic Schistosoma mansoni infection can present as a moderate or severe disease, termed intestinal or hepatosplenic schistosomiasis, respectively. Similarly, either moderate splenomegaly or hypersplenomegaly syndrome develops in CBA/J mice by 20weeks of infection and is similar to intestinal or hepatosplenic schistosomiasis respectively. Using this mouse model and two-dimensional differential in gel electrophoresis, the liver proteomic signatures of uninfected mice and mice infected for 6, 8, 12, or 20weeks were compared, and significant protein spots identified using mass spectrometry. We found the greatest number of changes at 12weeks suggesting that this period represents the peak time of change. Pathway analysis identified specific proteins and pathways that correlated to the pathological changes indicative of severe disease, and these pathways were involved as early as 8weeks after infection. These findings provide insight into the development of severe liver pathology in schistosomiasis and may aid in developing biomarkers for hepatosplenic schistosomiasis.
慢性曼氏血吸虫感染可表现为中度或重度疾病,分别称为肠型或肝脾型血吸虫病。同样,CBA/J 小鼠在感染 20 周后会发展为中度或重度脾肿大综合征,分别类似于肠型或肝脾型血吸虫病。使用这种小鼠模型和二维差异凝胶电泳,比较了未感染小鼠和感染 6、8、12 或 20 周的小鼠的肝蛋白质组特征,并使用质谱法鉴定了显著的蛋白质斑点。我们发现,在 12 周时发生的变化最多,这表明这一时期是变化的高峰期。途径分析确定了与严重疾病的病理变化相关的特定蛋白质和途径,这些途径早在感染后 8 周就已涉及。这些发现为血吸虫病严重肝病理的发展提供了深入了解,并可能有助于开发肝脾型血吸虫病的生物标志物。