Choi K S
Department of Horse/Companion and Wild Animal Science, College of Ecology and Environmental Science, Kyungpook National University, Sangju 37224, Republic of Korea.
Iran J Vet Res. 2017 Winter;18(1):13-17.
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.
牛病毒性腹泻病毒(BVDV)是全球畜牧业中一种具有重要经济影响的病原体。根据其对培养细胞的影响,BVDV可分为细胞病变型(cp)和非细胞病变型(ncp)。已知BVDV会改变宿主的免疫反应。其中,主要组织相容性复合体(MHC)II类分子在免疫系统的发育和功能中起核心作用,在牛中由DR和DQ两种类型组成。在本研究中,我们调查了非细胞病变型BVDV1或非细胞病变型BVDV2感染的单核细胞上MHC II类分子的表达情况。通过流式细胞术(P<0.01)、mRNA水平定量(实时定量RT-PCR,P<0.01)和蛋白质免疫印迹法(P<0.001),我们发现与非细胞病变型BVDV1感染的细胞相比,非细胞病变型BVDV2感染的单核细胞中MHC II类DQ分子的表达显著降低。此外,与非细胞病变型BVDV1感染的单核细胞相比,非细胞病变型BVDV2感染的单核细胞中γ干扰素(IFN)的产生明显减少(P<0.001)。这些发现表明,非细胞病变型BVDV2导致MHC II类DQ分子表达降低和IFN产生减少,从而逃避免疫识别并抑制先天性免疫反应的抗病毒防御机制。因此,结果表明非细胞病变型BVDV1和非细胞病变型BVDV2与宿主先天性免疫反应的相互作用不同。因此,我们的数据为非细胞病变型BVDV2与非细胞病变型BVDV1不同,损害抗原呈递、无法控制病毒感染并导致更严重疾病的机制提供了见解。