Histamine levels in embryonic chicken livers infected with very virulent infectious bursal disease virus

被引:3
作者
Li, Yinju [1 ]
He, Lei [1 ]
Cheng, Xiangchao [1 ]
Li, Jing [1 ]
Jia, Yanyan [1 ]
Yang, Danfang [1 ]
机构
[1] Henan Univ Sci & Technol, Anim Sci & Technol Coll, Luoyang 471003, Peoples R China
关键词
Infectious bursal disease virus; Histamine; HDC; vvIBDV; Chicken embryo; HISTIDINE-DECARBOXYLASE; SERIAL PASSAGE; IMMUNE; IMMUNOHISTOCHEMISTRY; LIPOPOLYSACCHARIDE; DIFFERENTIATION; PATHOGENICITY; RECEPTORS; TURKEYS; IMPACT;
D O I
10.1016/j.vetimm.2015.08.012
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Histamine is an endogenous nitrogenous compound with extensive effects on immunologic cells and involved in many physiological functions. The current aim was to determine histamine levels in embryonic liver and its association with the pathogenicity of a very virulent infectious bursal disease virus (vvIBDV) isolate serially passaged in chicken embryos. A vvIBDV isolate and the passaged viruses were inoculated into SPF embryonated chicken eggs (0.2 ml per egg) via the chorioallantoic membrane. Embryonic livers were collected at 24, 48, 72, 96, and 120 h post-inoculation and histamine contents were quantified by fluorescence spectrophotometry analyses. Results showed that the histamine content in embryonic livers infected with the original vvIBDV isolate and the early passaged viruses significantly increased 48 h post-inoculation, as compared with the adapted IBDV isolate (p < 0.01) and controls (p < 0.01), with the concentration peaking from 72 h to 96 h. Most of the infected chicken embryos died from 48 h to 96 h post-inoculation. Moreover, the histamine content in dead embryos was markedly increased compared with live embryos (p < 0.05), peaking at 72 h post-inoculation (p < 0.01). There was an association between histamine content in embryonic livers and an elevation in histidine decarboxylase activity. Taken together, our results suggest that an excess of histamine correlates with inflammatory responses during vvIBDV infection. This study provides an incremental step in the understanding of the pathogenesis of vvIBDV. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:91 / 96
页数:6
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