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全基因组CRISPR筛选揭示唾液酸在猪流行性腹泻病毒和猪冠状病毒感染中的关键作用。

Genome-wide CRISPR screen reveals key role of sialic acids in PEDV and porcine coronavirus infections.

作者信息

Guo Guanghao, Zhang Mengjia, Xu Zhuojia, Xi Peng, Zhu Hongmei, Evers Anouk, Lebbink Robert Jan, Lang Yifei, He Qigai, Huang Yao-Wei, Li Tiehai, Bosch Berend Jan, Li Wentao

机构信息

National Key Laboratory of Agricultural Microbiology, Hubei Hongshan Laboratory, College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, China.

State Key Laboratory of Chemical Biology, Carbohydrate-Based Drug Research Center, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.

出版信息

mBio. 2025 Aug 6:e0162825. doi: 10.1128/mbio.01628-25.

DOI:10.1128/mbio.01628-25
PMID:40767522
Abstract

Porcine epidemic diarrhea virus (PEDV) is a globally distributed alphacoronavirus with economic importance that can cause severe watery diarrhea and even death in piglets. To identify host factors essential for PEDV infection, we performed a genome-wide CRISPR/Cas9 screen in human hepatocellular carcinoma cells (Huh7) using the highly virulent PEDV GIIb strain GDU. Several genes involved in the sialic acid and heparan sulfate biosynthesis pathway and cholesterol metabolism were highly enriched following PEDV selection. We validated that the host factor ST3 beta-galactoside alpha-2,3-sialyltransferase 4 (ST3GAL4), which catalyzes the transfer of sialic acid to sugar chains via α2,3-linked linkages, is important for PEDV infection. To systematically investigate the role of sialic acid in PEDV infection, we knocked out genes related to sialic acid synthesis. This led to a reduced abundance of sialic acid on the cell surface, which in turn inhibited PEDV adsorption and internalization. Furthermore, we found that both α2,3-linked and α2,6-linked sialic acids can serve as cellular attachment factors for PEDV. We conducted a glycan microarray screen to determine which sialoglycans are preferred by the PEDV spike protein. The results revealed that PEDV favors binding to α2,3-sialoglycans. Additionally, we found that not only current circulating PEDV strains but also other porcine coronaviruses rely on sialic acid for efficient infection. Collectively, our findings provide insights into critical host factors involved in PEDV infection and demonstrate that disrupting genes involved in sialic acid biosynthesis negatively affects the infectivity of multiple porcine enteric coronaviruses.IMPORTANCEA wide range of viruses utilize sialic acid as receptors. Sialic acid binding may serve as a key determinant of viral host range. Different viruses exhibit distinct preferences for specific types of sialic acid linkages. However, it remains unclear which specific subtypes of sialic acid are utilized during PEDV infection. In this study, we performed CRISPR-based genome-wide knockout screening and identified ST3GAL4 as a key host factor for PEDV infection. Furthermore, we found that both α2,3-linked and α2,6-linked sialic acids can function as attachment factors for PEDV infection. A glycan microarray screen revealed that PEDV S1 shows the strongest binding preference for α2,3-linked and α2,8-linked sialosides. Sialic acids were also implicated in infections by other porcine enteric coronaviruses. Overall, our findings advance our understanding of viral entry mechanisms of PEDV and other swine coronaviruses and may provide avenues for designing antiviral strategies.

摘要

猪流行性腹泻病毒(PEDV)是一种全球分布的甲型冠状病毒,具有重要经济意义,可导致仔猪严重水样腹泻甚至死亡。为了确定PEDV感染所必需的宿主因子,我们使用高致病性PEDV GIIb株GDU在人肝癌细胞(Huh7)中进行了全基因组CRISPR/Cas9筛选。在PEDV筛选后,参与唾液酸和硫酸乙酰肝素生物合成途径以及胆固醇代谢的几个基因高度富集。我们验证了宿主因子ST3β-半乳糖苷α-2,3-唾液酸转移酶4(ST3GAL4)对PEDV感染很重要,该酶通过α2,3连接催化唾液酸转移到糖链上。为了系统研究唾液酸在PEDV感染中的作用,我们敲除了与唾液酸合成相关的基因。这导致细胞表面唾液酸丰度降低,进而抑制了PEDV的吸附和内化。此外,我们发现α2,3连接和α2,6连接的唾液酸都可以作为PEDV的细胞附着因子。我们进行了聚糖微阵列筛选,以确定PEDV刺突蛋白更喜欢哪种唾液酸聚糖。结果显示PEDV倾向于与α2,3-唾液酸聚糖结合。此外,我们发现不仅当前流行的PEDV毒株,其他猪冠状病毒也依赖唾液酸进行有效感染。总的来说,我们的研究结果为PEDV感染所涉及的关键宿主因子提供了见解,并表明破坏参与唾液酸生物合成的基因会对多种猪肠道冠状病毒的感染性产生负面影响。

重要性

多种病毒利用唾液酸作为受体。唾液酸结合可能是病毒宿主范围的关键决定因素。不同病毒对特定类型的唾液酸连接表现出不同的偏好。然而,PEDV感染期间使用的是哪种特定的唾液酸亚型仍不清楚。在本研究中,我们进行了基于CRISPR的全基因组敲除筛选,并确定ST3GAL4是PEDV感染的关键宿主因子。此外,我们发现α2,3连接和α2,6连接的唾液酸都可以作为PEDV感染的附着因子。聚糖微阵列筛选显示PEDV S1对α2,3连接和α2,8连接的唾液酸苷表现出最强的结合偏好。唾液酸也与其他猪肠道冠状病毒的感染有关。总体而言,我们的研究结果推进了我们对PEDV和其他猪冠状病毒病毒进入机制的理解,并可能为设计抗病毒策略提供途径。

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