Juan Mozas-Gutierrez
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Juan Mozas-Gutierrez has a total of 5 co-authors. Here are the top co-authors by number of shared publications:
- Alvaro Ras-Carmona
Department of Immunology, Ophthalmology and ENT, Faculty of Medicine, University Complutense of Madrid, Pza Ramon y Cajal S/N, 28040 Madrid, Spain
1 shared publication - Hector F. Pelaez-Prestel
Laboratory of Immunomedicine & Immunoinformatics, Department of Immunology, Ophthalmology and ORL (IO2), School of Medicine, Complutense University of Madrid
1 shared publication - Pedro Antonio Reche
Department of Immunology, Ophthalmology and ENT, Faculty of Medicine, Complutense University of Madrid, Pza Ramon y Cajal s/n, 28040 Madrid, Spain
1 shared publication - Raquel Reyes
Department of Immunology, Ophthalmology and ENT, Faculty of Medicine, Complutense University of Madrid, Pza Ramon y Cajal s/n, 28040 Madrid, Spain
1 shared publication - Sara Alonso Fernandez
Department of Immunology, Ophthalmology and ENT, Faculty of Medicine, Complutense University of Madrid, Pza Ramon y Cajal s/n, 28040 Madrid, Spain
1 shared publication
Latest Publications
- Open Access
- 19 August 2024
- Published by MDPI AG in Biomedicines
- Vol. 12 (8) , 1885
Eucalyptus Essential Oil Inhibits Cell Infection by SARS-CoV-2 Spike Pseudotyped Lentivirus
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) remains a public health concern due to infections with new SARS-CoV-2 variants. Therefore, finding effective preventive and therapeutic treatments against all SARS-CoV-2 variants is of great interest. In this study, we examined the capacity of eucalyptus essential oil (EEO) and eucalyptol (EOL) to prevent SARS-CoV-2 infection, using as a model SARS-CoV-2 Spike pseudotyped lentivirus (SARS-CoV-2 pseudovirus) and 293T cells transfected with human angiotensin-converting enzyme 2 (hACE2-293T cells). First, we determined the cytotoxicity of EEO and EOL using the MTT colorimetric assay, selecting non-cytotoxic concentrations ≤ 0.1% (v/v) for further analysis. Subsequently, we evaluated the capacity of EEO and EOL in cell cultures to preclude infection of hACE2-293T cells by SARS-CoV-2 pseudovirus, using a luciferase-based assay. We found that EEO and EOL significantly reduced SARS-CoV-2 pseudovirus infection, obtaining IC50 values of 0.00895% and 0.0042% (v/v), respectively. Likewise, EEO and EOL also reduced infection by vesicular stomatitis virus (VSV) pseudovirus, although higher concentrations were required. Hence, EEO and EOL may be able to inhibit SARS-CoV-2 infection, at least partially, through a Spike-independent pathway, supporting the implementation of aromatherapy with these agents as a cost-effective antiviral measure.
- 19 August 2024
- Published by MDPI AG in Biomedicines
- Vol. 12 (8) , 1885
Open AccessEucalyptus Essential Oil Inhibits Cell Infection by SARS-CoV-2 Spike Pseudotyped Lentivirus
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) remains a public health concern due to infections with new SARS-CoV-2 variants. Therefore, finding effective preventive and therapeutic treatments against all SARS-CoV-2 variants is of great interest. In this study, we examined the capacity of eucalyptus essential oil (EEO) and eucalyptol (EOL) to prevent SARS-CoV-2 infection, using as a model SARS-CoV-2 Spike pseudotyped lentivirus (SARS-CoV-2 pseudovirus) and 293T cells transfected with human angiotensin-converting enzyme 2 (hACE2-293T cells). First, we determined the cytotoxicity of EEO and EOL using the MTT colorimetric assay, selecting non-cytotoxic concentrations ≤ 0.1% (v/v) for further analysis. Subsequently, we evaluated the capacity of EEO and EOL in cell cultures to preclude infection of hACE2-293T cells by SARS-CoV-2 pseudovirus, using a luciferase-based assay. We found that EEO and EOL significantly reduced SARS-CoV-2 pseudovirus infection, obtaining IC50 values of 0.00895% and 0.0042% (v/v), respectively. Likewise, EEO and EOL also reduced infection by vesicular stomatitis virus (VSV) pseudovirus, although higher concentrations were required. Hence, EEO and EOL may be able to inhibit SARS-CoV-2 infection, at least partially, through a Spike-independent pathway, supporting the implementation of aromatherapy with these agents as a cost-effective antiviral measure.