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首页> 外文期刊>Microbial Pathogenesis >Gastrointestinal microbiota and mucosal immune gene expression in neonatal pigs reared in a cross-fostering model
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Gastrointestinal microbiota and mucosal immune gene expression in neonatal pigs reared in a cross-fostering model

机译:在交叉培育模型中饲养新生猪中的胃肠微生物和粘膜免疫基因表达

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Cross fostering is employed to equalize the number of piglet between litters ensuring colostrum intake for their survival and growth. However, little is known about the impact of cross fostering on the intestinal microbiota and mucosal immune gene expression of the neonatal pig. The objective of this study was to determine the influence of maternal microbial communities on the gastrointestinal (GI) microbiota and mucosal immune gene expression in young pigs reared in a cross-fostering model. Piglets were given high quality colostrum from birth dam or foster dam upon birth. Twenty-four piglets were randomly assigned at birth to 1 of 3 treatments according to colostrum source and postcolostral milk feeding during, as follow: treatment 1 (n = 8), received colostrum and post-colostral milk feeding from their own dam; treatment 2 (n = 8), received colostrum from foster dam and returned to their own dam for post-colostral milk feeding; and treatment 3 (n = 8), received colostrum and post-colostral milk feeding from foster dam. Genomic DNA was extracted, and the V1-V3 hypervariable region of the bacterial 16S rRNA gene was amplified and sequenced using the Illumina MiSeq platform. Quantitative real-time PCR analysis was also performed to quantify the expression of toll-like receptors (TLR) 2, TLR 4, TLR 10, tumor necrosis factor alpha (TNF alpha), interferon gamma (IFN gamma), and interleukin (IL) 4 and IL 10. Data analysis revealed that microbial communities were varied according to the GI biogeographical location, with colon being the most diverse section. Bacterial communities in both maternal colostrum and vaginal samples were significantly associated with those present in the fecal samples of piglets. Cross-fostering did not affect bacterial communities present in the piglet GI tract. However, the mRNA expression of TLR and inflammatory cytokines changed (P & 0.05) with biogeographical location in the GI tract, Higher mRNA expression of TLR and inflammatory cytokines was observed in ileum and ileum associated lymph tissues. This study suggests an impact of colostrum and maternal microbial communities on the microbiota development and mucosal immune gene expression in the newly born piglet. This study revealed novel information about the distribution and expression patterns of TLR and inflammatory cytokines in the GI tract of the young pig. Future studies are needed to determine the role and clinical importance of the mucosal microbiota and mucosal gene expression in health, productivity, and susceptibility to the development of GI disease, in piglets.
机译:通过交叉培养,用于均衡凋落物之间的仔猪数量,确保初乳摄入量的存活和生长。然而,关于交叉培养对新生猪的肠道微生物和粘膜免疫基因表达的影响几乎不了解。本研究的目的是确定母体微生物群落对在交叉培育模型中饲养的幼猪中的胃肠道(GI)微生物和粘膜免疫基因表达的影响。在出生时从出生大坝或寄养水坝获得高质量的初乳。根据初乳源和后脑乳牛奶在出生时随机分配二十四只仔猪,如初乳源和后喉咙牛奶进料,如下:治疗1(n = 8),接受初乳和从其自己的大坝喂养的初乳和初乳后牛奶;治疗2(n = 8),从寄养大坝接受初乳,并返回自己的水坝,用于后鼻孔牛奶喂养;和治疗3(n = 8),接受初乳和从培养大坝的后牛奶牛奶。提取基因组DNA,并使用Illumina MiSeq平台扩增并测序细菌16SRRNA基因的V1-V3高变区域。还进行定量实时PCR分析以量化Toll样受体(TLR)2,TLR 4,TLR 10,肿瘤坏死因子α(TNFα),干扰素γ(IFNγ),以及白细胞介素(IL)的表达4和IL 10.数据分析表明,微生物社区根据GI生物地理位置而变化,结肠是最多样化的部分。母性初乳和阴道样品中的细菌群落与仔猪粪便样品中存在的那些有显着相关。交叉培养并未影响仔猪GI道中存在的细菌社区。然而,TLR和炎性细胞因子的mRNA表达发生(P& 0.05),在GI道中,在回肠和回肠相关淋巴组织中观察到TLR和炎性细胞因子的较高mRNA表达。本研究表明初生和母体微生物社区对新出生仔猪的微生物群发育和粘膜免疫基因表达的影响。本研究揭示了关于幼猪的胃肠杆菌中TLR和炎性细胞因子的分布和表达模式的新信息。需要进行未来的研究来确定仔细,生产力和粘膜基因表达的作用和临床重要性和粘膜基因表达对仔猪疾病的发育中的健康,生产力和易感性。

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