Whittington R
NSW Agriculture, Elizabeth Macarthur Agricultural Institute, Menangle, Australia.
J Vet Diagn Invest. 1996 Jul;8(3):315-23. doi: 10.1177/104063879600800307.
The antigens extracted from Dichelobacter nodosus with potassium thiocyanate were analyzed by western blotting with sera from footrot-free sheep and from sheep infected with D. nodosus to identify components specific for infection. Several components with molecular mass < 33 kD were associated with infection, particularly bands of 32.5 kD, 30.5 kD, and 28 kD. Components with molecular mass > 56 kD may be responsible for false-positive reactions observed when sera of footrot-free sheep react with the potassium thiocyanate extract in solid phase enzyme-linked immunosorbent assays (ELISAs). Bands of 62.5 kD, 56 kD, 40 kD, and 19 kD were recognized for most sheep regardless of their disease status or ELISA reactivity and therefore do not appear to be detected by the ELISA. No components of the potassium thiocyanate extract were completely specific for infection. Antigens in the extract were identified primarily on the cell envelope by immunogold electron microscopy. Labeling was concentrated in the periplasm, with minor labeling of the cell surface. The extract consisted of tangled strands of particles with electron-dense cores, and few vesicular structures were observed.
用硫氰酸钾从结节拟杆菌中提取抗原,并用来自无腐蹄病绵羊和感染结节拟杆菌绵羊的血清进行蛋白质免疫印迹分析,以鉴定感染特异性成分。几种分子量<33 kD的成分与感染有关,特别是32.5 kD、30.5 kD和28 kD的条带。分子量>56 kD的成分可能是在固相酶联免疫吸附测定(ELISA)中无腐蹄病绵羊血清与硫氰酸钾提取物反应时观察到的假阳性反应的原因。无论绵羊的疾病状态或ELISA反应性如何,大多数绵羊都能识别出62.5 kD、56 kD、40 kD和19 kD的条带,因此似乎ELISA检测不到这些条带。硫氰酸钾提取物中没有成分对感染具有完全特异性。通过免疫金电子显微镜观察到提取物中的抗原主要位于细胞包膜上。标记集中在周质中,细胞表面标记较少。提取物由带有电子致密核心的缠结颗粒链组成,几乎没有观察到囊泡结构。