Faculdade de Medicina Veterinária e Zootecnia, Botucatu, UNESP - Univ Estadual Paulista, Botucatu, CEP 18618-000, São Paulo, Brazil.
Vet Microbiol. 2013 Jan 25;161(3-4):339-43. doi: 10.1016/j.vetmic.2012.07.024. Epub 2012 Aug 25.
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-1α (IL-1α), IL-1β, IL-6, IL-10, IL-12, interferon-γ (INF-γ) and tumour necrosis factor-α (TNF-α) 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-1β and IL-1α), testicles (INF-γ and IL-12), bulbourethral glands (IL-6 and TNF-α) and ampolae (INF-γ, IL-10, IL-1β and IL-1α). 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-1β and IL-1α), testicles (INF-γ and IL-12), and ampolae (INF-γ, IL-10, IL-1β and IL-1α), with the exception of the bulbourethral glands (IL-6 and TNF-α) 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.
绵羊布鲁氏菌病由绵羊布鲁氏菌引起,具有生殖组织嗜性,但细菌持续存在的机制尚不清楚。为了研究绵羊布鲁氏菌的发病机制和可能与细菌嗜性和持续存在相关的免疫机制,本研究在实验感染粗糙毒力株绵羊布鲁氏菌(R-B.ovis)后 8 个月,对公羊进行了研究。采用实时定量 RT-PCR(qRT-PCR)方法,定量检测了生殖组织(附睾、睾丸、壶腹、精囊和尿道球腺)和非生殖组织(肝、脾和肾)中白细胞介素 1α(IL-1α)、IL-1β、IL-6、IL-10、IL-12、干扰素-γ(INF-γ)和肿瘤坏死因子-α(TNF-α)的信使 RNA(mRNA)表达水平。在感染后 30、60、120 和 240 天(dpi)。在感染的急性期(30 dpi),宿主免疫反应最为显著,生殖组织中多种细胞因子上调,包括附睾(IL-6、IL-1β 和 IL-1α)、睾丸(INF-γ 和 IL-12)、尿道球腺(IL-6 和 TNF-α)和壶腹(INF-γ、IL-10、IL-1β 和 IL-1α)。在感染的发展过程中,细胞因子基因表达水平下降,表明免疫抑制和免疫逃避有利于慢性 R-B.ovis 感染的持续存在。在慢性 R-B.ovis 感染期(120 和 240 dpi),附睾(IL-1β 和 IL-1α)、睾丸(INF-γ 和 IL-12)和壶腹(INF-γ、IL-10、IL-1β 和 IL-1α)中细胞因子的产生受到下调,除了尿道球腺(IL-6 和 TNF-α)和附睾(IL-6);在这些组织中,R-B.ovis 感染导致促炎细胞因子 IL-6 的上调。本研究报告了实验感染粗糙毒力株绵羊布鲁氏菌的公羊组织中细胞因子的表达谱,与细菌持续存在和巨噬细胞激活有关。