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Establishment of Replication Deficient Vesicular Stomatitis Virus for Studies of PEDV Spike-Mediated Cell Entry and Its Inhibition

Overview
Journal Microorganisms
Specialty Microbiology
Date 2023 Aug 26
PMID 37630636
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Abstract

The porcine epidemic diarrhea virus (PEDV) is a highly contagious and virulent enteric coronavirus that causes severe enteric disease in pigs worldwide. PEDV infection causes profound diarrhea, vomiting, and dehydration in pigs of all ages, resulting in high mortality rates, particularly among neonatal piglets. The spike glycoprotein (S) of PEDV plays a crucial role in binding to the host cell receptor and facilitating fusion between the viral and host membranes. Pseudotyped viral particles featuring the PEDV S protein are valuable tools for investigating virus entry, identifying neutralizing antibodies, and developing small molecules to impede virus replication. In this study, we used a codon-optimized PEDV S protein to generate recombinant pseudotyped vesicular stomatitis virus (VSV) particles (rVSV-ΔG-EGFP-S). The full-length S protein was efficiently incorporated into VSV particles. The S protein pseudotyped VSV exhibited infectivity towards permissive cell lines of PEDV. Moreover, we identified a new permissive cell line, JHH7, which showed robust support for PEDV replication. In contrast to the SARS-CoV-2 spike protein, the removal of amino acids from the cytoplasmic tail resulted in reduced efficiency of viral pseudotyping. Furthermore, we demonstrated that 25-hydroxycholesterol inhibited rVSV-ΔG-EGFP-S entry, while human APN facilitated rVSV-ΔG-EGFP-S entry through the use of ANPEP knockout Huh7 cells. Finally, by transducing swine intestinal organoids with the rVSV-ΔG-EGFP-S virus, we observed efficient infection of the swine intestinal organoids by the PEDV spike-pseudotyped VSV. Our work offers valuable tools for studying the cellular entry of PEDV and developing interventions to curb its transmission.

Citing Articles

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Rizatdinova S, Ershova A, Astrakhantseva I Biomolecules. 2025; 15(1).

PMID: 39858529 PMC: 11763035. DOI: 10.3390/biom15010135.

References
1.
Li B, Ge J, Li Y . Porcine aminopeptidase N is a functional receptor for the PEDV coronavirus. Virology. 2007; 365(1):166-72. PMC: 7103304. DOI: 10.1016/j.virol.2007.03.031. View

2.
Liu C, Tang J, Ma Y, Liang X, Yang Y, Peng G . Receptor usage and cell entry of porcine epidemic diarrhea coronavirus. J Virol. 2015; 89(11):6121-5. PMC: 4442452. DOI: 10.1128/JVI.00430-15. View

3.
Zhang S, Cao Y, Yang Q . Transferrin receptor 1 levels at the cell surface influence the susceptibility of newborn piglets to PEDV infection. PLoS Pathog. 2020; 16(7):e1008682. PMC: 7419007. DOI: 10.1371/journal.ppat.1008682. View

4.
Zhang M, Lv L, Cai H, Li Y, Gao F, Yu L . Long-Term Expansion of Porcine Intestinal Organoids Serves as an Model for Swine Enteric Coronavirus Infection. Front Microbiol. 2022; 13:865336. PMC: 8967161. DOI: 10.3389/fmicb.2022.865336. View

5.
Zhang Y, Song Z, Wang M, Lan M, Zhang K, Jiang P . Cholesterol 25-hydroxylase negatively regulates porcine intestinal coronavirus replication by the production of 25-hydroxycholesterol. Vet Microbiol. 2019; 231:129-138. PMC: 7117535. DOI: 10.1016/j.vetmic.2019.03.004. View