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Kicker, E; Kouros, A; Zatloukal, K; Harant, H.
The Virus Entry Pathway Determines Sensitivity to the Antiviral Peptide TAT-I24.
Viruses. 2025; 17(4): Doi: 10.3390/v17040458 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Leading authors Med Uni Graz
Kicker Eva
Zatloukal Kurt
Co-authors Med Uni Graz
Kouros Antonio Nikolaos
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Abstract:
The peptide TAT-I24, a fusion of the TAT peptide (amino acids 48-60) and the 9-mer peptide I24, has been previously shown to neutralize several double-stranded (ds) DNA viruses in vitro. We have now extended the testing to potentially sensitive RNA viruses and analyzed the antiviral effect of the peptide against Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2). In Vero E6 cells, TAT-I24 neutralized the human 2019-nCoV isolate (Wuhan variant) in a dose-dependent manner, while it was unable to neutralize two SARS-CoV-2 variants of concern, Delta and Omicron. Moreover, TAT-I24 could not significantly neutralize any of the SARS-CoV-2 variants in the human lung carcinoma cell line Calu-3, which provides an alternative entry route for SARS-CoV-2 by direct membrane fusion. Therefore, a possible dependence on virus uptake by endocytosis was investigated by exposing Vero E6 cells to chloroquine (CQ), an inhibitor of endosomal acidification. The Wuhan variant was highly sensitive to inhibition by CQ, an effect which was further enhanced by TAT-I24, while the Delta variant was less sensitive to inhibition by higher concentrations of CQ compared to the Wuhan variant. The microscopic analysis of COS-7 cells using a rhodamine-labeled TAT-I24 (Rho-TAT-I24) showed the endosomal localization of fluorescent TAT-I24 and co-localization with transfected GFP-Rab14 but not GFP-Rab5. As these proteins are found in distinct endosomal pathways, our results indicate that the virus entry pathway determines sensitivity to the peptide.
Find related publications in this database (using NLM MeSH Indexing)
Animals - administration & dosage
Chlorocebus aethiops - administration & dosage
Vero Cells - administration & dosage
SARS-CoV-2 - drug effects, physiology
Virus Internalization - drug effects
Antiviral Agents - pharmacology
Humans - administration & dosage
Chloroquine - pharmacology
COVID-19 - virology
Peptides - pharmacology
Endocytosis - drug effects

Find related publications in this database (Keywords)
antiviral peptide
SARS-CoV-2
virus entry
endocytosis
Rab14
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