4.7 Article

Changes in the small intestine mucosal immune barrier in Muscovy ducklings infected with Muscovy duck reovirus

Journal

VETERINARY MICROBIOLOGY
Volume 233, Issue -, Pages 85-92

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.vetmic.2019.04.017

Keywords

Muscovy duck reovirus; Muscovy duckling; Mucosal immune barrier

Funding

  1. College of Animal Sciences FAFU [2018K005]
  2. Natural Science Foundation of China [31372474]
  3. Natural Science Foundation of Fujian Province [2017J01597]

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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-1 beta, 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.

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