Graduate School of Biosphere Science, Hiroshima University, Higashi-Hiroshima 739-8528, Japan.
Graduate School of Biosphere Science, Hiroshima University, Higashi-Hiroshima 739-8528, Japan.
Theriogenology. 2014 May;81(8):1129-38. doi: 10.1016/j.theriogenology.2014.02.002. Epub 2014 Feb 8.
The aim of this study was to determine the mechanism by which the avian infectious bronchitis virus (IBV) affects eggshell formation. Attenuated IBV (aIBV group) or vehicle (control group) was injected into the oviductal magnum lumen of White Leghorn laying hens. The changes in the expression of genes related to eggshell formation (collagen types I and V, and CaBP-D28K), densities of cytotoxic cells (CD8(+) and TCR-γδ(+) T cells), and gene expression of molecules related to cytotoxic immunoreaction (B-NK, perforin, granzyme, and IL-2) and proinflammatory cytokines (IL-1β, IL-6 and IFN-γ) were examined by quantitative reverse transcriptase polymerase chain reaction or immunohistochemistry in the isthmus and uterus. Gene expression of IL-1β and IL-6receptors in the tubular gland cells of the isthmus and uterus was analyzed by reverse transcriptase polymerase chain reaction. Gene expression of collagen type I, but not collagen type V, in the isthmus and CaBP-D28K in the uterus was decreased in the aIBV group compared with that in the control. The frequencies of CD8(+) cells and TCR-γδ(+) T cells in the isthmus and uterus were significantly higher in the aIBV group than in the control group. The expression of cytotoxic molecular and proinflammatory cytokines was also higher in the aIBV group than in the control. The expression of IL-6 receptor, but not IL-1β receptor, was identified in the tubular gland cells in the isthmus and uterus. These results suggest that IBV infection causes disorder of eggshell formation by disturbing gene expression of collagen type I in the isthmus and CaBP-D28K in the uterus, probably via the effects of substances from cytotoxic cells and proinflammatory cytokines.
本研究旨在确定禽传染性支气管炎病毒(IBV)影响蛋壳形成的机制。将弱毒 IBV(aIBV 组)或载体(对照组)注入白来航产蛋鸡的输卵管壶腹部腔。通过定量逆转录聚合酶链反应或免疫组织化学方法检测与蛋壳形成相关的基因(胶原 I 和 V 型和 CaBP-D28K)、细胞毒性细胞(CD8+和 TCR-γδ+T 细胞)密度以及与细胞毒性免疫反应相关的分子(B-NK、穿孔素、颗粒酶和 IL-2)和促炎细胞因子(IL-1β、IL-6 和 IFN-γ)的基因表达,在峡部和子宫中。通过逆转录聚合酶链反应分析峡部管状腺细胞和子宫中 IL-1β 和 IL-6 受体的基因表达。与对照组相比,aIBV 组峡部胶原 I 基因表达减少,但胶原 V 基因表达不变,而子宫 CaBP-D28K 基因表达减少。与对照组相比,aIBV 组峡部和子宫中 CD8+细胞和 TCR-γδ+T 细胞的频率明显更高。aIBV 组细胞毒性分子和促炎细胞因子的表达也高于对照组。在峡部和子宫的管状腺细胞中鉴定出 IL-6 受体,但未鉴定出 IL-1β 受体。这些结果表明,IBV 感染通过干扰峡部胶原 I 和子宫 CaBP-D28K 的基因表达,可能通过细胞毒性细胞和促炎细胞因子的物质作用,导致蛋壳形成紊乱。