Jia Xinzheng, Nie Qinghua, Zhang Xiquan, Nolan Lisa K, Lamont Susan J
Department of Animal Genetics, Breeding and Reproduction, College of Animal Science, South China Agricultural University, Guangzhou, Guangdong, China.
Guangdong Provincial Key Lab of Agro-Animal Genomics and Molecular Breeding and Key Laboratory of Chicken Genetics, Breeding and Reproduction, Ministry of Agriculture, Guangzhou, Guangdong, China.
Infect Immun. 2016 Dec 29;85(1). doi: 10.1128/IAI.00688-16. Print 2017 Jan.
Avian pathogenic Escherichia coli (APEC) causes one of the most common bacterial diseases of poultry worldwide. Effective control methods are therefore desirable and will be facilitated by a better understanding of the host response to the pathogen. Currently, microRNAs (miRNAs) involved in host resistance to APEC are unknown. Here, we applied RNA sequencing to explore the changed miRNAs and deregulated genes in the spleen of three groups of broilers: nonchallenged (NC), APEC-challenged with mild pathology (CM), and APEC-challenged with severe pathology (CS). Twenty-seven differentially expressed miRNAs (fold change >1.5; P value <0.01) were identified, including 13 miRNAs between the NC and CM, 17 between the NC and CS, and 14 between the CM and CS groups. Through functional analysis of these miRNA targets, 12 immune-related biological processes were found to be significantly enriched. Based on combined analyses of differentially expressed miRNAs and mRNAs within each of the three groups, 43 miRNA-mRNA pairs displayed significantly negative correlations (r < -0.8). Notably, gga-miR-429 was greatly increased in the CS group compared to levels in both the CM and NC groups. In vitro, gga-miR-429 directly repressed luciferase reporter gene activity via binding to 3' untranslated regions of TMEFF2, NTRK2, and SHISA2. Overexpression of gga-miR-429 in the HD11 macrophage cell line significantly inhibited TMEFF2 and SHISA2 expression, which are involved in the lipopolysaccharide-induced platelet-derived growth factor (PDGF) and Wnt signaling pathways. In summary, we provide the first report characterizing the miRNA changes during APEC infection, which may help to shed light on the roles of these recently identified genetic elements in the mechanisms of host resistance and susceptibility to APEC.
禽致病性大肠杆菌(APEC)引发了全球家禽中最常见的细菌性疾病之一。因此,需要有效的控制方法,而更好地了解宿主对病原体的反应将有助于实现这一目标。目前,参与宿主对APEC抗性的微小RNA(miRNA)尚不清楚。在此,我们应用RNA测序来探索三组肉鸡脾脏中变化的miRNA和失调的基因:未受挑战的(NC)、受到APEC挑战且病理症状较轻的(CM)以及受到APEC挑战且病理症状严重的(CS)。共鉴定出27个差异表达的miRNA(倍数变化>1.5;P值<0.01),其中NC组和CM组之间有13个miRNA,NC组和CS组之间有17个,CM组和CS组之间有14个。通过对这些miRNA靶标的功能分析,发现12个免疫相关的生物学过程显著富集。基于对三组中差异表达的miRNA和mRNA的联合分析,43对miRNA-mRNA对呈现出显著的负相关(r < -0.8)。值得注意的是,与CM组和NC组相比,CS组中的gga-miR-429大幅增加。在体外,gga-miR-429通过与TMEFF2、NTRK2和SHISA2的3'非翻译区结合直接抑制荧光素酶报告基因活性。在HD11巨噬细胞系中过表达gga-miR-429显著抑制了TMEFF2和SHISA2的表达,这两种基因参与脂多糖诱导的血小板衍生生长因子(PDGF)和Wnt信号通路。总之,我们首次报道了APEC感染期间miRNA的变化特征,这可能有助于揭示这些最近发现的遗传元件在宿主对APEC的抗性和易感性机制中的作用。