State Key Laboratory of Veterinary Etiological Biology, Lanzhou Institute of Veterinary Research, China Academy of Agricultural Sciences, Lanzhou, China.
PLoS One. 2013 May 30;8(5):e64236. doi: 10.1371/journal.pone.0064236. Print 2013.
Coccidiosis, caused by various Eimeria species, is a major parasitic disease in chickens. However, our understanding on how chickens respond to coccidian infection is highly limited at both molecular and cellular levels. The present study employed the Affymetrix chicken genome array and performed transcriptome analysis on chicken cecal epithelia in response to infection for 4.5 days in vivo by the cecal-specific species E. tenella. By Significance Analysis of Microarrays (SAM), we have identified 7,099 probe sets with q-values at <0.05, in which 4,033 and 3,066 genes were found to be up- or down-regulated in response to parasite infection. The reliability of the microarray data were validated by real-time qRT-PCR of 20 genes with varied fold changes in expression (i.e., correlation coefficient between microarray and qRT-PCR datasets: R (2) = 0.8773, p<0.0001). Gene ontology analysis, KEGG pathway mapping and manual annotations of regulated genes indicated that up-regulated genes were mainly involved in immunity/defense, responses to various stimuli, apoptosis/cell death and differentiation, signal transduction and extracellular matrix (ECM), whereas down-regulated genes were mainly encoding general metabolic enzymes, membrane components, and some transporters. Chickens mustered complex cecal eipthelia molecular and immunological responses in response to E. tenella infection, which included pathways involved in cytokine production and interactions, natural killer cell mediated cytotoxicity, and intestinal IgA production. In response to the pathogenesis and damage caused by infection, chicken cecal epithelia reduced general metabolism, DNA replication and repair, protein degradation, and mitochondrial functions.
球虫病是由各种艾美耳属种引起的一种主要的鸡寄生性疾病。然而,我们对鸡对球虫感染的反应在分子和细胞水平上的理解非常有限。本研究采用 Affymetrix 鸡基因组芯片,对体内感染盲肠特异性种艾美尔球虫(E. tenella)4.5 天的鸡盲肠上皮进行转录组分析。通过显著性分析微阵列(SAM),我们确定了 7099 个 q 值<0.05 的探针集,其中 4033 个和 3066 个基因分别上调或下调,以响应寄生虫感染。通过实时 qRT-PCR 对 20 个表达差异较大的基因进行验证(即微阵列和 qRT-PCR 数据集之间的相关系数:R2=0.8773,p<0.0001)。基因本体分析、KEGG 通路映射和调控基因的手动注释表明,上调基因主要参与免疫/防御、对各种刺激的反应、凋亡/细胞死亡和分化、信号转导和细胞外基质(ECM),而下调基因主要编码一般代谢酶、膜成分和一些转运体。鸡对艾美尔球虫感染产生了复杂的盲肠上皮分子和免疫反应,包括细胞因子产生和相互作用、自然杀伤细胞介导的细胞毒性和肠 IgA 产生的途径。为了应对感染引起的发病机制和损伤,鸡盲肠上皮降低了一般代谢、DNA 复制和修复、蛋白质降解和线粒体功能。