二肽基肽酶4是猪流行性腹泻病毒感染的辅助因子。

IF 2.4 2区 农林科学 Q3 MICROBIOLOGY Veterinary microbiology Pub Date : 2025-02-01 DOI:10.1016/j.vetmic.2025.110370
Yanjie Huang , Jiayun Wu , Xueli Zhang , Shuai Zhang , Shenglong Wu , Wenbin Bao
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引用次数: 0

摘要

猪流行性腹泻病毒(PEDV)是冠状病毒科甲型冠状病毒属的一种病毒,在新生仔猪中死亡率高达100% %,给养猪业造成巨大的经济损失。PEDV感染的靶细胞是猪小肠上皮细胞,其侵袭机制尚不清楚。我们的研究发现二肽基肽酶4 (DPP4)通过促进PEDV的侵袭和复制而作为PEDV感染的辅助因子。首先,我们绘制了DPP4在7日龄仔猪不同组织中的表达谱,发现DPP4在仔猪的肝、肺、肾、十二指肠、空肠和回肠组织中均有高表达。此外,免疫组化结果显示,DPP4主要分布在仔猪空肠肠绒毛上皮细胞的顶端。进一步研究发现,与未感染pedv的对照组相比,感染pedv的猪空肠组织和IPEC-J2细胞中DPP4的表达显著降低。DPP4抑制剂和特异性抗体可抑制PEDV的侵袭和复制。此外,敲除DPP4能够显著抑制PEDV感染。然后,我们发现内源性DPP4与PEDV相互作用,并且PEDV与内源性DPP4预孵育降低了病毒感染。最后,我们用硅预测了DPP4与PEDV-S1-RBD蛋白的对接,显示出很强的结合趋势。综上所述,我们的研究支持了DPP4是PEDV感染的辅助因子的假设。
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Dipeptidyl peptidase 4 is a cofactor for porcine epidemic diarrhea virus infection
Porcine epidemic diarrhea virus (PEDV) is a member of the genus Alphacoronavirus in the family Coronaviridae, which has a mortality rate of up to 100 % in neonatal piglets and causes huge economic losses to the pig industry. The target cells of PEDV infection are porcine small intestinal epithelial cells, and the mechanism of PEDV invasion remains unclear. Our study found that dipeptidyl peptidase 4 (DPP4) acts as a cofactor for PEDV infection by promoting PEDV invasion and replication. Firstly, we mapped the expression profile of DPP4 in different tissues of 7-day-old piglets and found that DPP4 was highly expressed in the liver, lung, kidney, duodenum, jejunum, and ileum tissues of piglets. In addition, the immunohistochemical results showed that DPP4 was mainly distributed at the apical of intestinal villous epithelial cells in the jejunum of piglets. Further studies revealed that DPP4 expression was significantly lower in PEDV-infected porcine jejunal tissues and IPEC-J2 cells than in uninfected controls. PEDV invasion and replication could be inhibited by DPP4 inhibitor and specific antibody. Moreover, DPP4 knockout was able to significantly inhibit PEDV infection. Then, we found that endogenous DPP4 interacted with PEDV, and that preincubation of PEDV with endogenous DPP4 reduced viral infection. Finally, we predicted the docking of DPP4 and PEDV-S1-RBD proteins in silico, showing a strong binding tendency. Taken together, our study supports the hypothesis that DPP4 is a cofactor for PEDV infection.
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来源期刊
Veterinary microbiology
Veterinary microbiology 农林科学-兽医学
CiteScore
5.90
自引率
6.10%
发文量
221
审稿时长
52 days
期刊介绍: Veterinary Microbiology is concerned with microbial (bacterial, fungal, viral) diseases of domesticated vertebrate animals (livestock, companion animals, fur-bearing animals, game, poultry, fish) that supply food, other useful products or companionship. In addition, Microbial diseases of wild animals living in captivity, or as members of the feral fauna will also be considered if the infections are of interest because of their interrelation with humans (zoonoses) and/or domestic animals. Studies of antimicrobial resistance are also included, provided that the results represent a substantial advance in knowledge. Authors are strongly encouraged to read - prior to submission - the Editorials (''Scope or cope'' and ''Scope or cope II'') published previously in the journal. The Editors reserve the right to suggest submission to another journal for those papers which they feel would be more appropriate for consideration by that journal. Original research papers of high quality and novelty on aspects of control, host response, molecular biology, pathogenesis, prevention, and treatment of microbial diseases of animals are published. Papers dealing primarily with immunology, epidemiology, molecular biology and antiviral or microbial agents will only be considered if they demonstrate a clear impact on a disease. Papers focusing solely on diagnostic techniques (such as another PCR protocol or ELISA) will not be published - focus should be on a microorganism and not on a particular technique. Papers only reporting microbial sequences, transcriptomics data, or proteomics data will not be considered unless the results represent a substantial advance in knowledge. Drug trial papers will be considered if they have general application or significance. Papers on the identification of microorganisms will also be considered, but detailed taxonomic studies do not fall within the scope of the journal. Case reports will not be published, unless they have general application or contain novel aspects. Papers of geographically limited interest, which repeat what had been established elsewhere will not be considered. The readership of the journal is global.
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