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The effect of bovine viral diarrhea virus on bovine monocyte phenotype

机译:牛病毒性腹泻病毒对牛单核细胞表型的影响

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摘要

Bovine viral diarrhea virus (BVDV) is an economically important pathogen of the livestock industry worldwide. BVDV is classified into cytopathic (cp) and noncytopathic (ncp), depending on its effects on cultured cells. BVDV is known to alter the host’s immune response. Of this, major histocompatibility complex (MHC) class II molecules play a central role in the development and function of the immune system, and are comprised of two types, DR and DQ, in cattle. In this study, we investigated the expression of MHC class II on monocytes infected with ncp BVDV1 or ncp BVDV2. Using flow cytometry (P<0.01), mRNA level quantification (quantitative real time RT-PCR, P<0.01), and western blot (P<0.001), we found that the expressions of MHC class IIDQ was significantly decreased in ncp BVDV2-infected monocytes compared with that in ncp BVDV1-infected cells. Furthermore, interferon gamma (IFN) production was markedly decreased in ncp BVDV2-infected monocytes (P<0.001) compared to those with ncp BVDV1 infection. These findings suggest that ncp BVDV2 causes reduced expressions of MHC class II DQ and a decreased production of IFN, resulting in evasion of immune recognition and suppression of the antiviral defense mechanism of the innate immune response. Consequently, the results demonstrate that ncp BVDV1 and ncp BVDV2 interact differently with the host innate immune response. Thus, our data provide insight into the mechanism by which, unlike ncp BVDV1, ncp BVDV2 impairs antigen presentation, fails to control the viral infection, and causes more severe disease.
机译:牛病毒性腹泻病毒(BVDV)是全世界畜牧业的重要经济病原体。 BVDV取决于对培养细胞的作用,可分为细胞病变(cp)和非细胞病变(ncp)。已知BVDV会改变宿主的免疫反应。其中,主要的组织相容性复合体(MHC)II类分子在免疫系统的发育和功能中起着核心作用,在牛中由DR和DQ两种类型组成。在这项研究中,我们调查了MHC II类在被ncp BVDV1或ncp BVDV2感染的单核细胞上的表达。使用流式细胞仪(P <0.01),mRNA水平定量(实时定量RT-PCR,P <0.01)和western blot(P <0.001),我们发现ncp BVDV2-中MHC IIDQ的表达显着降低。感染的单核细胞与ncp BVDV1感染的细胞相比。此外,与感染ncp BVDV1的单核细胞相比,感染ncp BVDV2的单核细胞的干扰素γ(IFN)产生显着降低(P <0.001)。这些发现表明,ncp BVDV2导致II类MHC DQ的表达减少,IFN的产生减少,从而导致逃避了免疫识别并抑制了先天免疫应答的抗病毒防御机制。因此,结果表明ncp BVDV1和ncp BVDV2与宿主先天免疫反应的相互作用不同。因此,我们的数据提供了对机制的了解,与ncp BVDV1不同,ncp BVDV2破坏了抗原呈递,无法控制病毒感染并导致更严重的疾病。

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