首页> 外文期刊>Veterinary Microbiology >Rough virulent strain of Brucella ovis induces pro- and anti-inflammatory cytokines in reproductive tissues in experimentally infected rams
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Rough virulent strain of Brucella ovis induces pro- and anti-inflammatory cytokines in reproductive tissues in experimentally infected rams

机译:布鲁氏菌粗糙毒株在实验感染的公羊的生殖组织中诱导促炎和抗炎细胞因子

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The ovine brucellosis caused by Brucella ovis has tropism for reproductive tissues but until now the mechanism of bacterial persistence is not understood. Cytokine expression profiles were studied for 8 months in rams after being experimentally infected with the rough virulent strain of B. ovis (R-B. ovis) to study the pathogenesis of B. ovis and immune mechanism possibly associated to bacteria tropism and persistence. The messenger RNA (mRNA) expression levels of interleukin-1 alpha (IL-1 alpha), IL-1 beta, IL-6, IL-10, IL-12, interferon-gamma (INF-gamma) and tumour necrosis factor-a (TNF-alpha) cytokines were quantified by real-time quantitative RT-PCR (qRT-PCR) in reproductive tissues (epididymus, testicles, ampolae, vesicular glands and bulbourethral glands), and non-reproductive (liver, spleen and kidneys) tissues at 30, 60, 120 and 240 days post infection (dpi). During the acute phase of infection at 30 dpi, the host immune response was most notable demonstrating an up-regulation of several cytokines in reproductive tissues, including the epididymus (IL-6, IL-1 beta and IL-1 alpha), testicles (INF-gamma and IL-12), bulbourethral glands (IL-6 and TNF-alpha) and ampolae (INF-gamma, IL-10, IL-1 beta and IL-1 alpha). During the development of infection, cytokine gene expression levels decreased, providing evidence of immunosuppression and evidence of immune evasion that favoured persistence of chronic R-B. ovis infection. During the chronic phase of R-B. ovis infection (120 and 240 dpi), cytokine production was down-regulated in the epididymus (IL-1 beta and IL-1 alpha), testicles (INF-gamma and IL-12), and ampolae (INF-gamma, IL-10, IL-1 beta and IL-1 alpha), with the exception of the bulbourethral glands (IL-6 and TNF-alpha) and epididymus (IL-6); in these tissues, R-B. ovis infection resulted in up-regulation of the pro-inflammatory cytokine IL-6. Herein, we report cytokine expression profiles in tissues of rams experimentally infected with the rough strain of B. ovis, which are associated with bacterial persistence and macrophage activation. (C) 2012 Elsevier B.V. All rights reserved.
机译:由绵羊布鲁氏菌引起的绵羊布鲁氏菌病对生殖组织具有嗜性,但是直到现在为止细菌持久性的机制尚不清楚。在实验中,用粗糙的强毒力的牛双歧杆菌(R-B。ovis)感染后,在公羊中研究了细胞因子的表达特征,历时8个月,研究了牛双歧杆菌的发病机理以及可能与细菌嗜性和持久性有关的免疫机制。白介素-1α(IL-1α),IL-1β,IL-6,IL-10,IL-12,干扰素-γ(INF-γ)和肿瘤坏死因子-的信使RNA(mRNA)表达水平通过实时定量RT-PCR(qRT-PCR)对生殖组织(附睾,睾丸,安瓿,水泡腺和膀胱神经管腺)和非生殖组织(肝,脾和肾)中的(TNF-α)细胞因子进行定量感染后30、60、120和240天(dpi)的组织。在30 dpi的急性感染阶段,宿主的免疫反应最显着,表明生殖组织中的几种细胞因子上调,包括附睾(IL-6,IL-1 beta和IL-1 alpha),睾丸( INF-γ和IL-12),球脑腺(IL-6和TNF-α)和安瓿(INF-γ,IL-10,IL-1β和IL-1α)。在感染的发展过程中,细胞因子基因的表达水平下降,提供了免疫抑制的证据和免疫逃逸的证据,有利于慢性R-B的持续存在。绵羊感染。在R-B的慢性期。 ovis感染(120和240 dpi),附睾(IL-1 beta和IL-1 alpha),睾丸(INF-γ和IL-12)和安瓿(INF-γ,IL- 10,IL-1 beta和IL-1 alpha),除了球脑腺(IL-6和TNF-alpha)和附睾(IL-6);在这些组织中,R-B。绵羊感染导致促炎细胞因子IL-6上调。在本文中,我们报告了在实验中感染了B. ovis粗糙菌株的公羊组织中的细胞因子表达谱,这与细菌的持久性和巨噬细胞的活化有关。 (C)2012 Elsevier B.V.保留所有权利。

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