Johnson M I, Henson J B, Gorham J R
Am J Pathol. 1975 Nov;81(2):321-36.
In an attempt to document progression rate differences in the development of glomerular lesions in mink infected with Aleutian disease virus (ADV), the glomeruli of Aleutian and non-Aleutian mink experimentally infected with ADV were evaluated by light, fluorescent, and electron microscopy. The animals were also examined for the presence of interstitial infiltrate, neutrophils, and arterial lesions. One hundred percent of the Aleutian mink had glomerular cell proliferation and interstitial infiltrate, while 95% of the Aleutian and 41% of the non-Aleutian mink had neutrophilic infiltrates and arteritis, respectively. Of the non-Aleutian mink, 91, 83, 42, and 12.5% had glomerular cell proliferations, glomerular neutrophils, interstitial infiltrate, and arterial lesions in, that order. All the Aleutian mink had glomerular depositions of gamma-globulin (IgG) and complement (C3), whereas 75% of non-Aleutian mink had deposits of IgG and C3. One hundred percent of both genotypes had glomerular deposits of immunoglobulin M (IgM). Ultrastructural glomerular changes consisting primarily of depositions of granular electron-dense material on basement membranes were observed in Aleutian mink 6 weeks after infection and 12 weeks after infection in non-Aleutian mink. These findings document progression rate differences in the development of glomerular lesions in Aleutian disease-affected Aleutian and non-Aleutian mink. Further, they emphasize the need for exploration of pathogenetic mechanisms involved in progression rate differences in lesion development.
为了记录感染阿留申病病毒(ADV)的水貂肾小球病变发展过程中的进展速率差异,通过光学显微镜、荧光显微镜和电子显微镜对经实验感染ADV的阿留申和非阿留申水貂的肾小球进行了评估。还检查了这些动物是否存在间质浸润、中性粒细胞和动脉病变。100%的阿留申水貂有肾小球细胞增殖和间质浸润,而分别有95%的阿留申水貂和41%的非阿留申水貂有嗜中性粒细胞浸润和动脉炎。在非阿留申水貂中,依次有91%、83%、42%和12.5%出现肾小球细胞增殖、肾小球中性粒细胞、间质浸润和动脉病变。所有阿留申水貂的肾小球均有γ-球蛋白(IgG)和补体(C3)沉积,而75%的非阿留申水貂有IgG和C3沉积。两种基因型的水貂100%都有免疫球蛋白M(IgM)的肾小球沉积。在感染后6周的阿留申水貂和感染后12周的非阿留申水貂中观察到肾小球超微结构变化,主要表现为颗粒状电子致密物质沉积在基底膜上。这些发现记录了受阿留申病影响的阿留申和非阿留申水貂肾小球病变发展过程中的进展速率差异。此外,它们强调了探索病变发展过程中进展速率差异所涉及的发病机制的必要性。