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Bovine Viral Diarrhoea Virus Infection Disrupts Uterine Interferon Stimulated Gene Regulatory Pathways During Pregnancy Recognition in Cows

机译:牛病毒性腹泻病毒感染破坏了妊娠识别过程中子宫干扰素刺激的基因调控途径。

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摘要

In cattle, conceptus-derived interferon tau (IFNT) is the pregnancy recognition (PR) signal. Our previous studies showed that non-cytopathic bovine viral diarrhoea virus (ncpBVDV) infection inhibited IFNT-induced interferon stimulated gene (ISG) expression, potentially causing early embryonic death. This study investigated the effect of bovine viral diarrhoea virus (BVDV) infection on upstream regulatory pathways of ISG production using an established PR model. Uterine endometrial cells from 10 apparently healthy and BVDV free cows were cultured and treated with 0 or 100 ng/mL IFNT for 24 h in the presence or absence of ncpBVDV infection. Microarray and pathway analysis were used to determine the IFNT-induced upstream regulators. Expression of the genes associated with the identified pathways were quantified with qPCR. IFNT challenge activated the signalling pathways associated with IFN receptors, JAK1/TYK2, IRFs and STATs and ncpBVDV infection inhibited the activation of IFNT on this pathway. Inhibition of this upstream signalling pathway may thus reduce ISG production to disrupt maternal PR. In addition, the reduction of uterine immunity by ncpBVDV infection may predispose the animals to uterine infection, which in turn impairs their reproductive performance. This provides a mechanism of how BVDV infection leads to early pregnancy failure in cows.
机译:在牛中,源自概念的干扰素tau(IFNT)是妊娠识别(PR)信号。我们以前的研究表明,非细胞性牛病毒性腹泻病毒(ncpBVDV)感染抑制了IFNτ诱导的干扰素刺激基因(ISG)的表达,可能导致早期胚胎死亡。这项研究使用已建立的PR模型研究了牛病毒性腹泻病毒(BVDV)感染对ISG生产上游调节途径的影响。培养有10只明显健康且无BVDV的母牛的子宫内膜细胞,并在存在或不存在ncpBVDV感染的情况下,以0或100 ng / mLIFNτ处理24 h。使用微阵列和途径分析来确定IFNτ诱导的上游调节剂。用qPCR定量与所鉴定途径相关的基因的表达。 IFNτ攻击激活了与IFN受体,JAK1 / TYK2,IRF和STATs相关的信号传导途径,ncpBVDV感染抑制了IFNτ在该途径上的激活。因此,抑制该上游信号传导途径可以减少ISG的产生以破坏母体PR。此外,ncpBVDV感染会降低子宫免疫力,可能使动物容易患上子宫感染,进而损害其生殖能力。这提供了BVDV感染如何导致母牛早期妊娠失败的机制。

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