Rioux M-C, Carmona C, Acosta D, Ward B, Ndao M, Gibbs B F, Bennett H P, Spithill T W
Institute of Parasitology, McGill University, 21, 111 Lakeshore Road, Ste-Anne-de-Bellevue, Que., Canada H9X 3V9.
Int J Parasitol. 2008 Jan;38(1):123-36. doi: 10.1016/j.ijpara.2007.07.017. Epub 2007 Aug 14.
Serum biomarkers associated with Fasciola hepatica infection of Corriedale sheep were analysed during the first 12 weeks of infection using surface-enhanced laser desorption ionisation time of flight mass spectrometry (SELDI-TOF MS). In the discovery phase of analysis, pooled sera collected at week 0 and at each week p.i. to week 12 were fractionated by anion-exchange chromatography and the protein mass fingerprints obtained in individual fractions were in the M/z range 1.5-150 kDa. A total of 2302 protein clusters (peaks) were identified that varied between time-points following infection with peaks increasing or decreasing in intensity, or showing transient variation in intensity, during the 12 weeks of parasite challenge. In the validation phase, candidate biomarkers in sera of individual sheep at weeks 3 and 9 p.i. were analysed, identifying 100 protein peaks, many of which are small peptides <10 kDa in size: 54% of these peaks were up-regulated in intensity at week 3 or 9 p.i. Twenty-six biomarkers were chosen for further study, ranging in size from 1832 to 89,823 Da: six biomarkers were up-regulated at weeks 3 and 9 p.i., 16 biomarkers were up-regulated only at week 9 p.i. and four biomarkers were down-regulated at week 9 p.i. Two biomarkers up-regulated at week 9 were identified as transferrin (77.2 kDa) and Apolipoprotein A-IV (44.3 kDa), respectively. The results show that the interaction between the host and F. hepatica is complex, with changes in biomarker patterns beginning within 3 weeks of infection and either persisting to weeks 9-12 or showing transient changes during infection. Identification of biomarkers expressed during ovine fasciolosis may provide insights into mechanisms of pathogenesis and immunity to Fasciola and may assist in the rational development and delivery of vaccines.
在感染的前12周内,利用表面增强激光解吸电离飞行时间质谱(SELDI-TOF MS)分析了与考力代绵羊肝片吸虫感染相关的血清生物标志物。在分析的发现阶段,收集感染后第0周及感染后每周直至第12周的混合血清,通过阴离子交换色谱法进行分级分离,各分级中获得的蛋白质质量指纹图谱的质荷比范围为1.5 - 150 kDa。共鉴定出2302个蛋白质簇(峰),这些峰在感染后的不同时间点有所变化,在寄生虫攻击的12周内,峰的强度增加、减少或呈现强度的瞬时变化。在验证阶段,分析了感染后第3周和第9周个体绵羊血清中的候选生物标志物,鉴定出100个蛋白质峰,其中许多是大小小于10 kDa的小肽:这些峰中有54%在感染后第3周或第9周强度上调。选择了26种生物标志物进行进一步研究,其大小范围为1832至89,823 Da:6种生物标志物在感染后第3周和第9周上调,16种生物标志物仅在感染后第9周上调,4种生物标志物在感染后第9周下调。在感染后第9周上调的两种生物标志物分别被鉴定为转铁蛋白(77.2 kDa)和载脂蛋白A-IV(44.3 kDa)。结果表明,宿主与肝片吸虫之间的相互作用是复杂的,生物标志物模式的变化在感染后3周内开始,要么持续到第9 - 12周,要么在感染期间呈现瞬时变化。鉴定绵羊肝片吸虫病期间表达的生物标志物可能有助于深入了解发病机制和对肝片吸虫的免疫机制,并可能有助于疫苗的合理开发和应用。