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Analysis of Chicken Mucosal Immune Response to Eimeria tenella and Eimeria maxima Infection by Quantitative Reverse Transcription-PCR

机译:定量逆转录PCR定量分析鸡对艾美球虫和最大艾美球虫感染的粘膜免疫反应

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The recent cloning of chicken genes coding for interleukins, chemokines, and other proteins involved in immune regulation and inflammation allowed us to analyze their expression during infection with Eimeria. The expression levels of different genes in jejunal and cecal RNA extracts isolated from uninfected chickens and chickens infected with Eimeria maxima or E. tenella were measured using a precise quantitative reverse transcription-PCR technique. Seven days after E. tenellainfection, expression of the proinflammatory cytokine interleukin-1β (IL-1β) mRNA was increased 80-fold. Among the chemokines analyzed, the CC chemokines K203 (200-fold) and macrophage inflammatory factor 1β (MIP-1β) (80-fold) were strongly upregulated in the infected ceca, but the CXC chemokines IL-8 and K60 were not. However, the CXC chemokines were expressed at very high levels in uninfected cecal extracts. The levels of gamma interferon (IFN-γ) (300-fold), inducible nitric oxide synthase (iNOS) (200-fold), and myelomonocytic growth factor (MGF) (50-fold) were also highly upregulated during infection with E. tenella, whereas cyclooxygenase 2 showed a more modest (13-fold) increase. The genes upregulated during E. tenella infection were generally also upregulated during E. maxima infection but at a lower magnitude except for those encoding MIP-1β and MGF. For these two cytokines, no significant change in expression levels was observed after E. maximainfection. CD3+ intraepithelial lymphocytes may participate in the IFN-γ upregulation observed after infection, since both recruitment and upregulation of the IFN-γ mRNA level were observed in the infected jejunal mucosa. Moreover, in the chicken macrophage cell line HD-11, CC chemokines, MGF, IL-1β, and iNOS were inducible by IFN-γ, suggesting that macrophages may be one of the cell populations involved in the upregulation of these cytokines observed in vivo during infection with Eimeria.
机译:最近克隆了编码白细胞介素,趋化因子和其他涉及免疫调节和炎症的蛋白质的鸡基因,这使我们能够分析它们在 Eimeria 感染期间的表达。从未感染鸡和感染 Eimeria maxima E的鸡空肠和盲肠RNA提取物中不同基因的表达水平。使用精确的定量逆转录-PCR技术检测Tenella 。 E之后的7天。感染后,促炎细胞因子白介素-1β(IL-1β)mRNA的表达增加了80倍。在所分析的趋化因子中,CC趋化因子K203(200倍)和巨噬细胞炎性因子1β(MIP-1β)(80倍)在受感染的盲肠中强烈上调,而CXC趋化因子IL-8和K60则没有。但是,CXC趋化因子在未感染的盲肠提取物中以很高的水平表达。在感染期间,γ干扰素(IFN-γ)(300倍),诱导型一氧化氮合酶(iNOS)(200倍)和骨髓单核细胞生长因子(MGF)(50倍)的水平也被上调。 > E。 Tenella ,而环氧合酶2的增加幅度较小(13倍)。在E期,这些基因被上调。在 E期间,tenella 感染通常也被上调。最大感染,但编码MIP-1β和MGF的感染除外。对于这两种细胞因子,在 E后未观察到表达水平的显着变化。最大感染。 CD3 + 上皮内淋巴细胞可能参与感染后观察到的IFN-γ上调,因为在感染的空肠黏膜中均观察到IFN-γmRNA水平的募集和上调。此外,在鸡巨噬细胞HD-11细胞系中,IFN-γ可诱导CC趋化因子,MGF,IL-1β和iNOS,这表明巨噬细胞可能是体内观察到的这些细胞因子上调的细胞群之一。在感染艾美球虫期间。

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