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肠炎沙门氏菌肠炎血清型攻击后两个F8高级杂交鸡品系的全基因组表达谱

Global gene expression profile after Salmonella enterica Serovar enteritidis challenge in two F8 advanced intercross chicken lines.

作者信息

Zhou H, Lamont S J

机构信息

Department of Animal Science, Iowa State University, Ames, IA 50011, USA.

出版信息

Cytogenet Genome Res. 2007;117(1-4):131-8. doi: 10.1159/000103173.

Abstract

A chicken 13K cDNA microarray was used to profile global gene expression after Salmonella enteritidis (SE) challenge of young chickens. Two F8 advanced intercross lines (AIL), broiler by Leghorn, and broiler by Fayoumi, were studied. Day-old chicks were orally inoculated with SE, and spleens were harvested at day 7 or 8 post-inoculation. The SE bacteria burden in the spleen was quantified. The 20% high and 20% low SE burden birds within each AIL and harvest time were studied by microarray. The loop design was used for pair-comparison between high and low SE burden challenged birds and unchallenged birds, within each AIL and harvest time. The signal intensity of each gene was globally normalized and expressed on the natural log scale. A mixed model including line, treatment, time, array (random effect), dye, and all two-way interactions among treatment, time, and line was used to identify differentially expressed candidate genes at the 1% significance level. The results suggest that genetics, time, and interaction between genetics and time play important roles in gene regulation of SE infection and colonization in chickens. The differentially expressed genes identified in the current study are candidates for detailed hypothesis-driven investigation of genes determining resistance to SE in chickens.

摘要

利用鸡13K cDNA微阵列分析了雏鸡感染肠炎沙门氏菌(SE)后全基因组的表达情况。研究了两个F8高级杂交系(AIL),即肉鸡与来航鸡的杂交系以及肉鸡与法尤米鸡的杂交系。一日龄雏鸡经口接种SE,接种后第7天或第8天采集脾脏。对脾脏中的SE细菌载量进行了定量分析。在每个AIL和采集时间内,对SE细菌载量处于前20%的高载量鸡和后20%的低载量鸡进行了微阵列研究。采用环形设计,在每个AIL和采集时间内,对高SE细菌载量和低SE细菌载量的攻毒鸡与未攻毒鸡进行配对比较。对每个基因的信号强度进行全局归一化,并以自然对数尺度表示。使用包含品系、处理、时间、阵列(随机效应)、染料以及处理、时间和品系之间所有双向交互作用的混合模型,在1%的显著性水平上鉴定差异表达的候选基因。结果表明,遗传因素、时间以及遗传因素与时间之间的相互作用在鸡SE感染和定植的基因调控中发挥着重要作用。本研究中鉴定出的差异表达基因是用于详细的假设驱动研究的候选基因,这些研究旨在确定鸡对SE的抗性相关基因。

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