College of Animal Science and Technology, Gansu Agricultural University, Lanzhou, Gansu, China.
Guizhou Institute of Prataculture, Guizhou Academy of Agriculture Science, Guiyang, China.
PeerJ. 2022 Apr 4;10:e13006. doi: 10.7717/peerj.13006. eCollection 2022.
() type C is the principal pathogenic clostridia of swine, frequently causing hemorrhagic diarrhea, even necrotic enteritis in piglets, leading to severe economic loss for swine industr ies worldwide. However, there are no specific and effective prevention measures. Therefore, clarifying the molecular mechanisms of hosts against pathogenesis infection is very important to reduce the incidence of type C infected piglet diarrhea disease.
We performed an TMT labeling-based quantitative spleen proteomic analysis of the control group (SC), tolerance group (SR) and susceptible group (SS) to identify the differentially expressed proteins (DEPs), and screened potential molecular markers of piglet spleen tissues in response to type C infection.
In this study, a total of 115, 176 and 83 DEPs were identified in SR vs SC, SS vs SC, and SR vs SC, respectively, which may play the important regulatory roles in the process of piglet spleens in response to type C-infected diarrhea diseases. GO enrichment analysis revealed that the DEPs were mostly significantly enriched in acute inflammatory response, defense response, antimicrobial response, transporter activity, cellular metabolic process and so on, and KEGG pathway enrichment analysis showed that the significantly enriched immune related pathways of the PPAR signaling pathway, IL-17 signaling pathway, antigen processing and presentation, which hints at the immune defense process of piglet spleen against infection. This study helps to elucidate the protein expressional pattern of piglet spleen against type C-infected diarrhea disease, which can contribute to the prevention and control for pig diarrhea disease and the further development of diarrhea resistant pig breeding.
()型 C 是猪的主要致病梭菌,常引起仔猪出血性腹泻,甚至坏死性肠炎,给世界范围内的养猪业造成严重的经济损失。然而,目前尚无特异性和有效的预防措施。因此,阐明宿主对致病性感染的分子机制对于减少 C 型感染仔猪腹泻病的发病率非常重要。
我们对对照组(SC)、耐受力组(SR)和易感性组(SS)进行了基于 TMT 标记的定量脾脏蛋白质组学分析,以鉴定差异表达蛋白(DEPs),并筛选仔猪脾脏组织对 C 型感染反应的潜在分子标志物。
在这项研究中,分别在 SR 与 SC、SS 与 SC、SR 与 SC 之间鉴定到了 115、176 和 83 个 DEPs,它们可能在仔猪脾脏对 C 型感染性腹泻病的反应过程中发挥重要的调节作用。GO 富集分析表明,DEPs 主要显著富集在急性炎症反应、防御反应、抗菌反应、转运蛋白活性、细胞代谢过程等方面,KEGG 途径富集分析表明,显著富集的免疫相关途径包括过氧化物酶体增殖物激活受体信号通路、IL-17 信号通路、抗原加工和呈递等,这暗示了仔猪脾脏对 C 型感染的免疫防御过程。本研究有助于阐明仔猪脾脏对 C 型感染性腹泻病的蛋白质表达模式,有助于预防和控制猪腹泻病,并进一步开发抗腹泻猪的选育。