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牛抗胃肠道线虫机制的瘤胃转录组特征。

Characterization of the abomasal transcriptome for mechanisms of resistance to gastrointestinal nematodes in cattle.

机构信息

Bovine Functional Genomics Laboratory, Animal and Natural Resources Institute, USDA-ARS, Beltsville, MD 20705, USA.

出版信息

Vet Res. 2011 Nov 30;42(1):114. doi: 10.1186/1297-9716-42-114.

Abstract

The response of the abomasal transcriptome to gastrointestinal parasites was evaluated in parasite-susceptible and parasite-resistant Angus cattle using RNA-seq at a depth of 23.7 million sequences per sample. These cattle displayed distinctly separate resistance phenotypes as assessed by fecal egg counts. Approximately 65.3% of the 23,632 bovine genes were expressed in the fundic abomasum. Of these, 13,758 genes were expressed in all samples tested and likely represent core components of the bovine abomasal transcriptome. The gene (BT14427) with the most abundant transcript, accounting for 10.4% of sequences in the transcriptome, is located on chromosome 29 and has unknown functions. Additionally, PIGR (1.6%), Complement C3 (0.7%), and Immunoglobulin J chain (0.5%) were among the most abundant transcripts in the transcriptome. Among the 203 genes impacted, 64 were significantly over-expressed in resistant animals at a stringent cutoff (FDR < 5%). Among the 94 224 splice junctions identified, 133 were uniquely present: 90 were observed only in resistant animals, and 43 were present only in susceptible animals. Gene Ontology (GO) enrichment of the genes under study uncovered an association with lipid metabolism, which was confirmed by an independent pathway analysis. Several pathways, such as FXR/RXR activation, LXR/RXR activation, LPS/IL-1 mediated inhibition of RXR function, and arachidonic acid metabolism, were impacted in resistant animals, which are potentially involved in the development of parasite resistance in cattle. Our results provide insights into the development of host immunity to gastrointestinal nematode infection and will facilitate understanding of mechanism underlying host resistance.

摘要

利用 RNA-seq 技术,在每个样本深度为 2370 万条序列的条件下,对易感和抗寄生虫的安格斯牛的皱胃转录组对胃肠道寄生虫的反应进行了评估。这些牛通过粪便虫卵计数评估具有明显不同的抗性表型。在胃底皱胃中表达了大约 65.3%的 23632 个牛基因。其中,13758 个基因在所有测试样本中表达,可能代表牛皱胃转录组的核心组成部分。转录组中丰度最高的基因(BT14427),占转录组序列的 10.4%,位于 29 号染色体上,具有未知功能。此外,PIGR(1.6%)、补体 C3(0.7%)和免疫球蛋白 J 链(0.5%)也是转录组中丰度最高的转录本之一。在受影响的 203 个基因中,64 个在严格截止值(FDR<5%)下在抗性动物中显著过表达。在鉴定的 94224 个剪接接头中,有 133 个是唯一存在的:90 个仅在抗性动物中观察到,43 个仅在易感动物中存在。对所研究基因的基因本体论(GO)富集分析揭示了与脂质代谢的关联,这通过独立的途径分析得到了证实。在抗性动物中,一些途径如 FXR/RXR 激活、LXR/RXR 激活、LPS/IL-1 介导的 RXR 功能抑制和花生四烯酸代谢受到影响,这些途径可能参与了牛寄生虫抗性的发展。我们的研究结果为宿主对胃肠道线虫感染的免疫反应提供了新的见解,并将有助于理解宿主抗性的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c291/3260172/87136bde25b7/1297-9716-42-114-1.jpg

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