Liang Jia Qi, Xie Mei-Ying, Hou Lian-Jie, Wang Hai-Long, Luo Jun-Yi, Sun Jia-Jie, Xi Qian-Yun, Jiang Qing-Yan, Chen Ting, Zhang Yong-Liang
College of Animal Science, Guangdong Province Key Laboratory of Animal Nutritional Regulation, and National Engineering Research Center for Breeding Swine Industry, South China Agricultural University, Guangzhou, Guangdong, 510642, China.
Guangdong Eco-Engineering Polytechnic, Guangzhou, Guangdong, 510520, China.
Antiviral Res. 2023 Apr;212:105579. doi: 10.1016/j.antiviral.2023.105579. Epub 2023 Mar 11.
Porcine epidemic diarrhea virus (PEDV), a member of the genus Alphacoronavirus in the family Coronaviridae, causes acute diarrhea and/or vomiting, dehydration, and high mortality in neonatal piglets. It has caused huge economic losses to animal husbandry worldwide. Current commercial PEDV vaccines do not provide enough protection against variant and evolved virus strains. No specific drugs are available to treat PEDV infection. The development of more effective therapeutic anti-PEDV agents is urgently needed. Our previous study suggested that porcine milk small extracellular vesicles (sEV) facilitate intestinal tract development and prevent lipopolysaccharide-induced intestinal injury. However, the effects of milk sEV during viral infection remain unclear. Our study found that porcine milk sEV, which was isolated and purified by differential ultracentrifugation, could inhibit PEDV replication in IPEC-J2 and Vero cells. Simultaneously, we constructed a PEDV infection model for piglet intestinal organoids and found that milk sEV also inhibited PEDV infection. Subsequently, in vivo experiments showed that milk sEV pre-feeding exerted robust protection of piglets from PEDV-induced diarrhea and mortality. Strikingly, we found that the miRNAs extracted from milk sEV inhibited PEDV infection. miRNA-seq, bioinformatics analysis, and experimental verification demonstrated that miR-let-7e and miR-27b, which were identified in milk sEV targeted PEDV N and host HMGB1, suppressed viral replication. Taken together, we revealed the biological function of milk sEV in resisting PEDV infection and proved its cargo miRNAs, miR-let-7e and miR-27b, possess antiviral functions. This study is the first description of the novel function of porcine milk sEV in regulating PEDV infection. It provides a better understanding of milk sEV resistance to coronavirus infection, warranting further studies to develop sEV as an attractive antiviral.
猪流行性腹泻病毒(PEDV)是冠状病毒科甲型冠状病毒属的成员,可导致新生仔猪急性腹泻和/或呕吐、脱水及高死亡率。它给全球畜牧业造成了巨大经济损失。目前的商业化PEDV疫苗对变异和进化的病毒株防护不足。尚无治疗PEDV感染的特效药物。迫切需要研发更有效的抗PEDV治疗药物。我们之前的研究表明,猪乳小细胞外囊泡(sEV)有助于肠道发育并预防脂多糖诱导的肠道损伤。然而,病毒感染期间乳sEV的作用仍不清楚。我们的研究发现,通过差速超速离心分离纯化的猪乳sEV可抑制PEDV在IPEC-J2和Vero细胞中的复制。同时,我们构建了仔猪肠道类器官的PEDV感染模型,发现乳sEV也能抑制PEDV感染。随后的体内实验表明,预先投喂乳sEV能有效保护仔猪免受PEDV诱导的腹泻和死亡。令人惊讶的是,我们发现从乳sEV中提取的miRNA可抑制PEDV感染。miRNA测序、生物信息学分析和实验验证表明,在乳sEV中鉴定出的miR-let-7e和miR-27b靶向PEDV N和宿主HMGB1,抑制病毒复制。综上所述,我们揭示了乳sEV在抵抗PEDV感染中的生物学功能,并证明其携带的miRNA,即miR-let-7e和miR-27b具有抗病毒功能。本研究首次描述了猪乳sEV在调节PEDV感染中的新功能。它有助于更好地理解乳sEV对冠状病毒感染的抗性,值得进一步研究以开发sEV作为一种有吸引力的抗病毒剂。