Feline coronavirus influences the biogenesis and composition of extracellular vesicles derived from CRFK cells.

CRFK cells biogenesis exosomes extracellular vesicles feline coronavirus immunomodulation pandemic

Journal

Frontiers in veterinary science
ISSN: 2297-1769
Titre abrégé: Front Vet Sci
Pays: Switzerland
ID NLM: 101666658

Informations de publication

Date de publication:
2024
Historique:
received: 19 02 2024
accepted: 02 07 2024
medline: 2 8 2024
pubmed: 2 8 2024
entrez: 2 8 2024
Statut: epublish

Résumé

Coronavirus (CoV) has become a public health crisis that causes numerous illnesses in humans and certain animals. Studies have identified the small, lipid-bound structures called extracellular vesicles (EVs) as the mechanism through which viruses can enter host cells, spread, and evade the host's immune defenses. EVs are able to package and carry numerous viral compounds, including proteins, genetic substances, lipids, and receptor proteins. We proposed that the coronavirus could alter EV production and content, as well as influence EV biogenesis and composition in host cells. In the current research, Crandell-Rees feline kidney (CRFK) cells were infected with feline coronavirus (FCoV) in an exosome-free media at a multiplicity of infection (MOI) of 2,500 infectious units (IFU) at 48 h and 72 h time points. Cell viability was analyzed and found to be significantly decreased by 9% (48 h) and 15% (72 h) due to FCoV infection. EVs were isolated by ultracentrifugation, and the surface morphology of isolated EVs was analyzed via Scanning Electron Microscope (SEM). NanoSight particle tracking analysis (NTA) confirmed that the mean particle sizes of control EVs were 131.9 nm and 126.6 nm, while FCoV infected-derived EVs were 143.4 nm and 120.9 nm at 48 and 72 h, respectively. Total DNA, RNA, and protein levels were determined in isolated EVs at both incubation time points; however, total protein was significantly increased at 48 h. Expression of specific protein markers such as TMPRSS2, ACE2, Alix, TSG101, CDs (29, 47, 63), TLRs (3, 6, 7), TNF-α, and others were altered in infection-derived EVs when compared to control-derived EVs after FCoV infection. Our findings suggested that FCoV infection could alter the EV production and composition in host cells, which affects the infection progression and disease evolution. One purpose of studying EVs in various animal coronaviruses that are in close contact with humans is to provide significant information about disease development, transmission, and adaptation. Hence, this study suggests that EVs could provide diagnostic and therapeutic applications in animal CoVs, and such understanding could provide information to prevent future coronavirus outbreaks.

Identifiants

pubmed: 39091390
doi: 10.3389/fvets.2024.1388438
pmc: PMC11292801
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1388438

Informations de copyright

Copyright © 2024 Wijerathne, Pandit, Ipinmoroti, Crenshaw and Matthews.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Auteurs

Sandani V T Wijerathne (SVT)

Microbiology Program, Alabama State University, Montgomery, AL, United States.

Rachana Pandit (R)

Microbiology Program, Alabama State University, Montgomery, AL, United States.

Ayodeji O Ipinmoroti (AO)

Microbiology Program, Alabama State University, Montgomery, AL, United States.

Brennetta J Crenshaw (BJ)

Microbiology Program, Alabama State University, Montgomery, AL, United States.

Qiana L Matthews (QL)

Microbiology Program, Alabama State University, Montgomery, AL, United States.
Department of Biological Sciences, College of Science, Technology, Engineering, and Mathematics, Alabama State University, Montgomery, AL, United States.

Classifications MeSH