Sánchez-Cordón P J, Rodríguez-Sánchez B, Risalde M A, Molina V, Pedrera M, Sánchez-Vizcaíno J M, Gómez-Villamandos J C
Department of Comparative Pathology, Veterinary Faculty, University of Córdoba, Edificio Sanidad Animal, Campus de Rabanales, 14014 Córdoba, Spain.
J Comp Pathol. 2010 Jul;143(1):20-8. doi: 10.1016/j.jcpa.2009.12.017. Epub 2010 Feb 13.
The VP7 structural protein is the most abundant of the major core proteins and is highly conserved in all serotypes of bluetongue virus (BTV). The aim of this study was to develop immunohistochemical techniques for the detection of BTV VP7 in Bouin's- and formalin-fixed and paraffin wax-embedded tissues from small ruminants (sheep and goats) naturally infected with BTV. Tissue samples were taken from animals in which BTV infection had been confirmed by reverse transcriptase polymerase chain reaction. Optimal results were obtained by incubation of monoclonal antibody 2E9 on samples fixed with Bouin's solution or neutral buffered formalin. Optimum antigen retrieval for Bouin's-fixed samples was by microwave heating (6 min) of tissue samples in citrate buffer (pH 6.0, 0.01 M), while for formalin-fixed samples a 30 min heating period in pH 9.0 buffer was required. In both species, BTV was mainly detected in the spleen, lymph nodes and lungs; specifically within the arteriolar and capillary endothelial cells, together with macrophages and lymphocytes. The immunohistochemical method described will be a useful tool for future research.
VP7结构蛋白是主要核心蛋白中含量最丰富的,并且在蓝舌病病毒(BTV)的所有血清型中高度保守。本研究的目的是开发免疫组织化学技术,用于检测来自自然感染BTV的小反刍动物(绵羊和山羊)的经布因氏液和福尔马林固定、石蜡包埋组织中的BTV VP7。组织样本取自经逆转录聚合酶链反应确认感染BTV的动物。用单克隆抗体2E9孵育经布因氏液或中性缓冲福尔马林固定的样本可获得最佳结果。布因氏液固定样本的最佳抗原修复方法是将组织样本在柠檬酸盐缓冲液(pH 6.0,0.01 M)中微波加热(6分钟),而福尔马林固定样本则需要在pH 9.0缓冲液中加热30分钟。在这两个物种中,BTV主要在脾脏、淋巴结和肺中检测到;具体在小动脉和毛细血管内皮细胞内,以及巨噬细胞和淋巴细胞中。所描述的免疫组织化学方法将成为未来研究的有用工具。