生物技术通报 ›› 2019, Vol. 35 ›› Issue (11): 64-71.doi: 10.13560/j.cnki.biotech.bull.1985.2019-0257

• 研究报告 • 上一篇    下一篇

京海黄鸡柔嫩艾美耳球虫感染后盲肠转录组分析

于海亮1, 邹文斌1, 王晓慧1, 林雨鑫1, 2, 戴国俊1, 张涛1, 张跟喜1, 谢恺舟1, 王金玉1, 施会强3   

  1. 1. 扬州大学动物科学与技术学院,扬州 225009;
    2. 昆山市畜牧兽医站,昆山 215300;
    3. 江苏京海禽业集团有限公司,海门 226100
  • 收稿日期:2019-03-30 出版日期:2019-11-26 发布日期:2019-11-19
  • 作者简介:于海亮,男,硕士研究生,研究方向:家禽生产及抗病育种;E-mail:1596340072@qq.com
  • 基金资助:
    江苏省农业三新工程(SXGC[2017]298),江苏现代农业产业技术体系建设专项资金(JATS[2018]303),“十二五”国家科技支撑计划(2014BAD13B02),江苏省高校优势学科建设工程(PAPD),国家现代农业产业技术体系专项资金(CARS-41-G23)

RNA Sequencing Analysis of Cecum Tissues of Jinghai Yellow Chickens Infected by E. tenella

YU Hai-liang1, ZOU Wen-bin1, WANG Xiao-hui1, LIN Yu-xin1, 2, DAI Guo-jun1, ZHANG Tao1, ZHANG Gen-xi1, XIE Kai-zhou1, WANG Jin-yu1, SHI Hui-qiang3   

  1. 1. College of Animal Science and Technology,Yangzhou University,Yangzhou 225009;
    2. Animal Husbandry and Veterinary Station of Kunshan City,Kunshan 215300;
    3. Jiangsu Jinghai Poultry Group Co. Ltd,Haimen 226100
  • Received:2019-03-30 Published:2019-11-26 Online:2019-11-19

摘要: 为了探究京海黄鸡感染柔嫩艾美尔球虫(E. tenella)后盲肠组织差异表达基因,以及球虫感染分子应答过程和免疫应答机制,试验采用RNA-seq技术对E. tenella感染和非感染组第7天的盲肠组织进行转录组测序,筛选差异表达基因,并进行差异基因的功能、通路富集分析。结果表明,在感染和非感染组中有显著差异的表达基因2 830个(P<0.05),其中1 419个基因上调,1 411个基因下调。随机选取10个差异基因进行qRT-PCR验证,结果显示差异基因的表达倍数与RNA-seq检测结果显著相关(r=0.988,P<0.000),决定系数达0.975。GO分析表明,有2 356个差异基因获得GO功能注释,显著富集的前30个GO terms主要涉及细胞交流、信号转导、血管生成、氧化还原酶活性等。KEGG分析发现差异基因显著富集的信号通路有黏着斑、细胞外基质-受体相互作用、过氧化物酶体增殖物激活受体等。这些通路中的差异基因有ANGPTL4、ACSL5、VEGFC、CD44和MAKP10等,提示这些基因在宿主柔嫩艾美耳球虫感染过程中发挥重要作用。

关键词: 京海黄鸡, 柔嫩艾美尔球虫, 盲肠, 转录组测序, 差异表达基因

Abstract: This work aims to investigate the differentially expressed genes(DEGs)of cecal tissue of Jinghai yellow chickens infected with E. tenella and the molecular response process and immune response mechanism of the infection. The RNA-seq technique was used to sequence the cecal tissue of E. tenella-infected group and non-infected group on the 7th day of post-infection,and the DEGs were screened for functional and pathway enrichment analysis. The results indicated that there were 2 830 DEGs(P<0.05)between the infected and uninfected groups,of which 1 419 were up-regulated and 1 411 were down-regulated. Ten DEGs were randomly selected for qRT-PCR verification,and the results showed that the fold change of DEGs was highly consistent with the RNA-seq results(r=0.988,P<0.000),and the coefficient of determination reached 0.975. GO analysis showed that 2 356 DEGs were functionally annotated,and the top 30 significantly enriched GO terms involved mainly cell communication,signal transduction,angiogenesis,and oxidoreductase activity. The KEGG analysis revealed that top significantly enriched signaling pathways included focal adhesions,extracellular matrix-receptor interactions and peroxisome proliferator-activated receptors. Key DEGs in these pathways include ANGPTL4,ACSL5,VEGFC,CD44,and MAKP10,etc.,suggesting that these genes would play an important role in the infection of E. tenella.

Key words: Jinghai yellow chicken, E. tenella, cecum, RNA-seq, DEGs