Department of Animal Sciences, University of Illinois, Urbana, IL 61801, USA.
J Anim Sci. 2011 Oct;89(10):3016-29. doi: 10.2527/jas.2010-3366. Epub 2011 May 27.
This study characterized gene expression in peripheral blood mononuclear cells (PBMC) and bronchoalveolar lavage fluid (BALF) cells from control- or mannan oligosaccharide (MOS)-fed pigs with or without porcine reproductive and respiratory syndrome virus (PRRSV) at d 7 postinfection (PI). Weaned pigs (3 wk old) fed 0 or 0.2% MOS (Bio-Mos) diets were intranasally inoculated with PRRSV or a sterile medium at 5 wk of age. Total RNA (3 pigs/treatment) was extracted from cells. Double-stranded cDNA was amplified, labeled, and further hybridized to the Affymetrix GeneChip Porcine Genome Array consisting of 23,937 probe sets representing 20,201 genes. Microarray data were analyzed in R using packages from the Bioconductor project. Differential gene expression was tested by fitting a mixed linear model equivalent to a 2 × 2 factorial ANOVA using the limma package. Dietary MOS and PRRSV changed the expression of thousands of probe sets in PBMC and BALF cells (P < 0.05). The MOS × PRRSV interaction altered the expression of more nonimmune probe sets in PBMC (977 up, 1,128 down) than in BALF cells (117 up, 78 down). The MOS × PRRSV interaction (P < 0.05) for immune probe sets in PBMC affected genes encoding key inflammatory mediators. In uninfected pigs, gene expression of IL-1α, IL-6, myeloid differentiation factor 88, Toll-like receptor (TLR) 4, major histocompatibility complex (MHC) II, and dead box polypeptide 58 increased in PBMC of MOS-fed pigs (P < 0.05). This suggests that MOS enhances disease resistance in pigs and supports the fact that MOS induced a rapid increase in leukocytes at d 3 and 7 PI. Within infected pigs, however, MOS reduced the expression of IL-1β, IL-6, IL-8, macrophage inflammatory protein (MIP)-1α, MIP-1β, monocyte chemotactic protein (MCP)-1, and TLR4 genes in PBMC (P < 0.05). This finding may explain why fever was ameliorated in infected pigs fed MOS by d 7 PI. The expression of IL-1β, IL-6, MIP-1β, MCP-1, and TLR4 genes was confirmed by quantitative real-time reverse-transcription PCR. In BALF cells of infected pigs, MOS reduced the gene expression of TLR4, MHCII, and molecules associated with the complement system, but increased the gene expression of MHCI. In short, MOS regulated the expression of nonimmune and immune genes in pig leukocytes, perhaps providing benefits by enhancing the immune responses of the pigs to an infection, while preventing overstimulation of the immune system.
本研究旨在表征对照或甘露寡糖(MOS)喂养的猪外周血单个核细胞(PBMC)和支气管肺泡灌洗液(BALF)细胞中的基因表达,这些猪在感染猪繁殖与呼吸综合征病毒(PRRSV)后第 7 天(d7 PI)。在 5 周龄时,用 PRRSV 或无菌培养基经鼻腔接种 3 周龄断奶猪(0 或 0.2% MOS(Bio-Mos)饮食)。从细胞中提取总 RNA(3 头/处理)。用 Affymetrix GeneChip Porcine Genome Array 扩增、标记和进一步杂交双链 cDNA,该芯片包含 23937 个探针组,代表 20201 个基因。使用来自 Bioconductor 项目的 R 中的软件包分析微阵列数据。使用 limma 软件包拟合混合线性模型,该模型等效于 2×2 析因方差分析,以测试差异基因表达。膳食 MOS 和 PRRSV 改变了 PBMC 和 BALF 细胞中数千个探针组的表达(P<0.05)。MOS×PRRSV 相互作用改变了 PBMC 中非免疫探针组(977 个上调,1128 个下调)的表达,而在 BALF 细胞中(117 个上调,78 个下调)。在未感染的猪中,IL-1α、IL-6、髓样分化因子 88、Toll 样受体(TLR)4、主要组织相容性复合体(MHC)II 和 DEAD 框多肽 58 的基因表达在 MOS 喂养的猪的 PBMC 中增加(P<0.05)。这表明 MOS 增强了猪的抗病能力,并支持 MOS 在 d3 和 d7 PI 时快速增加白细胞的事实。然而,在感染的猪中,MOS 降低了 PBMC 中 IL-1β、IL-6、IL-8、巨噬细胞炎性蛋白(MIP)-1α、MIP-1β、单核细胞趋化蛋白(MCP)-1 和 TLR4 基因的表达(P<0.05)。这一发现可能解释了为什么在感染 MOS 的猪中,体温在 d7 PI 时得到改善。通过定量实时逆转录 PCR 证实了 IL-1β、IL-6、MIP-1β、MCP-1 和 TLR4 基因的表达。在感染猪的 BALF 细胞中,MOS 降低了 TLR4、MHCII 和补体系统相关分子的基因表达,但增加了 MHCI 的基因表达。总之,MOS 调节了猪白细胞中非免疫和免疫基因的表达,可能通过增强猪对感染的免疫反应,同时防止免疫系统过度刺激,从而提供益处。