College of Animal Science, Fujian Agriculture and Forestry University, Fuzhou 350002, People's Republic of China; Fujian Key Laboratory of Traditional Chinese Veterinary Medicine and Animal Health, Fujian Agricultural and Forestry University, Fuzhou 350002, People's Republic of China.
College of Animal Science, Fujian Agriculture and Forestry University, Fuzhou 350002, People's Republic of China.
Vet Microbiol. 2019 Jun;233:85-92. doi: 10.1016/j.vetmic.2019.04.017. Epub 2019 Apr 12.
Muscovy duck reovirus (MDRV) causes serious immunodeficiency in the intestinal mucosa, although the underlying histopathological mechanisms remain unclear. Thus, we investigated the impact of MDRV infection on intestinal morphology using hematoxylin and eosin staining. Immune-related cells were also quantified by staining with hematoxylin and eosin, toluidine blue, and periodic acid-Schiff stain, or by immunohistochemistry and cytochemistry for lectin. Similarly, CD4 and CD8 cells were quantified by flow cytometry, and the expression of several immune-related molecules was quantified by radioimmunoassay. We found that MDRV clearly damaged the intestinal mucosa, based on tissue morphology, villus length, villus width, intestinal thickness, villus height/crypt depth ratio, and villus surface area. MDRV also altered the density or distribution of lymphocytes, mastocytes, and goblet cells in the small intestinal mucosa, as well as microfold cells in Peyer's patches. In addition, MDRV markedly depleted CD4 cells from the intestinal mucosa and lowered the CD4:CD8 ratio in peripheral blood. Moreover, MDRV diminished the levels of secretory IgA and mucosal addressin cell adhesion molecule-1 (p < 0.01), but elevated those of histamine and nitric oxide (p < 0.01 or p < 0.05). Finally, MDRV significantly suppressed IL-1β, IL-4, IL-5, and IL-8 levels (p < 0.01 or p < 0.05) mid-infection. Collectively, our data suggest that MDRV severely damages the structure and function of the intestinal mucosa by modulating immune cells and immune-related factors, thus leading to local immunodeficiency. Our findings lay the foundation for further research on the pathogenesis of MDRV.
Muscovy 鸭呼肠孤病毒(Muscovy duck reovirus,MDRV)会导致肠道黏膜严重免疫缺陷,但其中的组织病理学机制尚不清楚。因此,我们使用苏木精和伊红染色法研究了 MDRV 感染对肠道形态的影响。我们还通过苏木精和伊红、甲苯胺蓝、过碘酸-Schiff 染色、免疫组织化学和凝集素细胞化学对免疫相关细胞进行了量化,通过流式细胞术对 CD4 和 CD8 细胞进行了量化,并通过放射免疫法对几种免疫相关分子的表达进行了量化。我们发现,基于组织形态、绒毛长度、绒毛宽度、肠壁厚度、绒毛高度/隐窝深度比和绒毛表面积,MDRV 明显损害了肠道黏膜。MDRV 还改变了小肠黏膜中淋巴细胞、肥大细胞和杯状细胞的密度或分布,以及派尔集合淋巴结中的微褶皱细胞。此外,MDRV 显著减少了肠道黏膜中的 CD4 细胞,并降低了外周血中的 CD4:CD8 比值。此外,MDRV 降低了分泌型 IgA 和黏膜地址素细胞黏附分子-1 的水平(p<0.01),但升高了组胺和一氧化氮的水平(p<0.01 或 p<0.05)。最后,MDRV 在感染中期显著抑制了 IL-1β、IL-4、IL-5 和 IL-8 的水平(p<0.01 或 p<0.05)。总之,我们的数据表明,MDRV 通过调节免疫细胞和免疫相关因子严重损害了肠道黏膜的结构和功能,从而导致局部免疫缺陷。我们的研究结果为进一步研究 MDRV 的发病机制奠定了基础。