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Influence of the structural development of bursa on the susceptibility of chickens to infectious bursal disease virus.

Poultry science (2016-06-12)
Sufen Zhao, Yuanyuan Jia, Deping Han, Haiyan Ma, Syed Zahid Ali Shah, Yunfei Ma, Kedao Teng
RÉSUMÉ

Infectious bursal disease (IBD), caused by IBD virus (IBDV), is an acute, highly contagious immunosuppressive avian disease. Although age-dependent changes in susceptibility of chickens to IBDV have been established, the relationship between age-dependent structural changes in bursa of Fabricius and susceptibility of chickens to IBDV is still unclear. In the present study, we examined the bursa anatomical structure and pathological changes in specific-pathogen-free (SPF) white leghorn chickens 0 to 8 weeks post hatch (w.p.h.) and IBDV BC6/85-infected SPF chickens 2 to 6 w.p.h. respectively, by histology, histopathology, immunohistochemistry, and transmission electron microscopy. Almost all IBDV-exposed chickens (2 to 6 w.p.h.) were infected, with the severest bursal inflammation and complication in chickens at 3 w.p.h. Furthermore, the bursae of healthy chickens at 3 to 6 w.p.h. had decreased laminin immunoreactivities, lots of splits, and irregular shapes in basement membrane (BM) of cortico-medullary epithelium (CME), irregularly arranged CME, and large numbers of immunoglobulin M-bearing (IgM+) B lymphocytes in the medulla. The decreased barrier function of corticomedullary border and large amount of IgM+ B lymphocytes provide a chance for IBDV to easily contact and infect target cells at 3 to 6 w.p.h. By contrast, regular BM, neatly arranged CME, and few IgM+ B lymphocytes in healthy chickens younger than 2 w.p.h., as well as reduced IgM+ B lymphocytes and high immunoglobulin A (IgA) content in healthy chickens older than 8 w.p.h., were observed, suggesting that the integrity of corticomedullary border barrier, a small amount of target cells and high IgA content of the bursa could be the reasons for these chickens being less susceptible to IBDV. Although studies have shown how IBDV affects bursa, we focus first on the age-dependent changes of CME, BM of CME and IgA content, and our findings are the first to elucidate the structural development of bursa in relation to IBDV susceptibility from a morphological perspective.

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Paraplast X-TRA®, for tissue embedding