文献类型： 外文期刊

作者： Chen, Si ¹ ; Wang, Chengqiang ¹ ; Chen, Qiaoling ¹ ; Zhao, Dantong ² ; Liu, Yongbin ³ ; Zhao, Shihua ⁴ ; Fu, Shaoyin ⁴ ; He, Xiaolong ⁴ ; Yang, Bin ⁴ ; Zhao, Qinan ⁴ ; An, Qi ¹ ; Zhang, Zhenxing ¹ ; Cheng, Yiwen ¹ ; Man, Churiga ¹ ; Liu, Guoying ² ; Wei, Xuefeng ² ; Zhang, Wenguang ⁵ ; Du, Li ¹ ; Wang, Fengyang ¹ ;

作者机构： 1.Hainan Univ, Coll Anim Sci & Technol, Hainan Key Lab Trop Anim Reprod, Anim Genet Engn Key Lab Haikou Breeding & Epidem, Haikou, Peoples R China

2.Jinyu Baoling Biopharmaceut Co Ltd, Hohhot, Peoples R China

3.Inner Mongolia Univ, Hohhot, Peoples R China

4.Inner Mongolia Acad Agr & Anim Husb Sci Hohhot Ch, Hohhot, Peoples R China

5.Inner Mongolia Agr Univ, Coll Anim Sci, Hohhot, Peoples R China

关键词： Brucella; sheep; lymphatic nodes; miRNAs; downregulation

期刊名称：FRONTIERS IN VETERINARY SCIENCE （ 影响因子：3.471； 五年影响因子：3.821 ）

ISSN：

年卷期： 2022 年 9 卷

页码：

收录情况： SCI

摘要： Ovine and caprine brucellosis, both caused by Brucella melitensis, lead to substantial economic losses in the animal industry and health problems in human populations. Brucella suis strain 2 (B.suis S2), as a live attenuated vaccine, is used extensively in China to prevent brucellosis. It has been proven that microRNA (miRNAs) are involved in the immunopathogenesis of brucellosis; however, the miRNA-driven mechanism of immune response to B.suis S2 in vivo remains unknown. To determine which new miRNAs are involved in the host immune response to B.suis S2 and elucidate the function of these miRNAs, we performed a comprehensive analysis of miRNA expression profiles in sheep immunized with B.suis S2 using the high-throughput sequencing approach. The submandibular lymphatic nodes from sheep seropositive for Brucella were collected at 7, 14, 21, 30, 60 and 90 days post-immunization. MiRNA sequencing analysis revealed that 282 differentially expressed miRNAs (|log(2) fold-change |>0.5 and p < 0.05) were significantly enriched in the immune pathways, including the NF-kappa B signaling pathway, B cell receptor signaling pathway, p53 signaling pathway and complement and coagulation cascades. Increasing the threshold to |log(2) fold change|>1 and p < 0.01 revealed 48 differentially expressed miRNAs, 31 of which were novel miRNAs. Thirteen of these novel miRNAs, which were differentially expressed for at least two time points, were detected via RT-qPCR assays. The novel_229, novel_609, novel_973 and oar-miR-181a assessed by RT-qPCR were detectable and consistent with the expression patterns obtained by miRNA sequencing. Functional analyses of these miRNAs demonstrated that their target genes participated in the immune response pathways, including the innate and adaptive immunity pathways. The immune-related target genes of novel_229 included ENSOARG00000000649 and TMED1, as well as LCN2, PDPK1 and LPO were novel_609 target genes. The immune-related target genes of novel_973 included C6orf58, SPPL3, BPIFB1, ENSOARG00000021083, MPTX1, CCL28, FGB, IDO1, OLR1 and ENSOARG00000020393. The immune-related target genes of oar-miR-181a included ENSOARG00000002722, ARHGEF2, MFAP4 and DOK2. These results will deepen our understanding of the host miRNA-driven defense mechanism in sheep immunized with B.suis S2 vaccine, and provide the valuable information for optimizing vaccines and developing molecular diagnostic targets.