Ivermectin reduces in vivo coronavirus infection in a mouse experimental model
Resumen:
The objective of this study was to test the effectiveness of ivermectin for the treatment of mouse hepatitis virus (MHV), a type 2 family RNA coronavirus similar to SARS-CoV-2. Female BALB/cJ mice were infected with 6,000 PFU of MHV-A59 (group infected, n = 20) or infected and then immediately treated with a single dose of 500 μg/kg ivermectin (group infected + IVM, n = 20) or were not infected and treated with PBS (control group, n = 16). Five days after infection/treatment, the mice were euthanized and the tissues were sampled to assess their general health status and infection levels. Overall, the results demonstrated that viral infection induced typical MHV-caused disease, with the livers showing severe hepatocellular necrosis surrounded by a severe lymphoplasmacytic inflammatory infiltration associated with a high hepatic viral load (52,158 AU), while mice treated with ivermectin showed a better health status with a lower viral load (23,192 AU; p < 0.05), with only a few having histopathological liver damage (p < 0.05). No significant differences were found between the group infected + IVM and control group mice (P = NS). Furthermore, serum transaminase levels (aspartate aminotransferase and alanine aminotransferase) were significantly lower in the treated mice than in the infected animals. In conclusion, ivermectin diminished the MHV viral load and disease in the mice, being a useful model for further understanding this therapy against coronavirus diseases.
| 2021 | |
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INFECCION EXPERIMENTAL RATONES IVERMECTINA CORONAVIRUS CAUSANTE DEL SINDROME RESPIRATORIO AGUDO SEVERO TERAPIA |
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| Inglés | |
| Universidad de la República | |
| COLIBRI | |
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https://hdl.handle.net/20.500.12008/48337
https://doi.org/10.1038/s41598-021-86679-0 |
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| Acceso abierto | |
| Licencia Creative Commons Atribución (CC - By 4.0) |
| _version_ | 1875693029974605824 |
|---|---|
| author | Arévalo, Ana Paula |
| author2 | Pagotto, Romina Pórfido Barayoli, Jorge Luis Daghero Villanueva, Hellen Segovia, Mercedes Yamasaki, Kanji Varela Cruces, María Belén Hill, Marcelo Verdes García, José Manuel Duhalde Vega, Maite Bollati-Fogolín, Mariela Crispo, Martina |
| author2_role | author author author author author author author author author author author |
| author_facet | Arévalo, Ana Paula Pagotto, Romina Pórfido Barayoli, Jorge Luis Daghero Villanueva, Hellen Segovia, Mercedes Yamasaki, Kanji Varela Cruces, María Belén Hill, Marcelo Verdes García, José Manuel Duhalde Vega, Maite Bollati-Fogolín, Mariela Crispo, Martina |
| author_role | author |
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| collection | COLIBRI |
| dc.contributor.filiacion.none.fl_str_mv | Arévalo Ana Paula, Institut Pasteur de Montevideo (Uruguay). Transgenic and Experimental Animal Unit Pagotto Romina, Institut Pasteur de Montevideo (Uruguay). Cell Biology Unit Pórfido Barayoli Jorge Luis, Institut Pasteur de Montevideo (Uruguay). Transgenic and Experimental Animal Unit / Institut Pasteur de Montevideo (Uruguay). Worm Biology Laboratory / Universidad de la República (Uruguay). Faculty of Chemistry. Department of Biosciences Daghero Villanueva Hellen, Institut Pasteur de Montevideo (Uruguay). Cell Biology Unit Segovia Mercedes, Institut Pasteur de Montevideo (Uruguay). Laboratory of Immunoregulation and Inflammation / Universidad de la República (Uruguay). Faculty of Medicine. Immunobiology Department Yamasaki Kanji, Universidad de la República (Uruguay). Veterinary Faculty. Department of Pathobiology. Pathology Unit Varela Cruces María Belén, Universidad de la República (Uruguay). Veterinary Faculty. Department of Pathobiology. Pathology Unit Hill Marcelo, Institut Pasteur de Montevideo (Uruguay). Laboratory of Immunoregulation and Inflammation / Universidad de la República (Uruguay). Faculty of Medicine. Immunobiology Department Verdes García José Manuel, Universidad de la República (Uruguay). Veterinary Faculty. Department of Pathobiology. Pathology Unit Duhalde Vega Maite, Institut Pasteur de Montevideo (Uruguay). Laboratory of Immunoregulation and Inflammation / University of Buenos Aires (Buenos Aires, Argentina). School of Pharmacy and Biochemistry. Institute of Biological Chemistry and Chemical Physics (UBA‑CONICET) Bollati-Fogolín Mariela, Institut Pasteur de Montevideo (Uruguay). Cell Biology Unit Crispo Martina, Institut Pasteur de Montevideo (Uruguay). Transgenic and Experimental Animal Unit |
| dc.creator.none.fl_str_mv | Arévalo, Ana Paula Pagotto, Romina Pórfido Barayoli, Jorge Luis Daghero Villanueva, Hellen Segovia, Mercedes Yamasaki, Kanji Varela Cruces, María Belén Hill, Marcelo Verdes García, José Manuel Duhalde Vega, Maite Bollati-Fogolín, Mariela Crispo, Martina |
| dc.date.accessioned.none.fl_str_mv | 2025-02-11T15:26:47Z |
| dc.date.available.none.fl_str_mv | 2025-02-11T15:26:47Z |
| dc.date.issued.none.fl_str_mv | 2021 |
| dc.description.abstract.none.fl_txt_mv | The objective of this study was to test the effectiveness of ivermectin for the treatment of mouse hepatitis virus (MHV), a type 2 family RNA coronavirus similar to SARS-CoV-2. Female BALB/cJ mice were infected with 6,000 PFU of MHV-A59 (group infected, n = 20) or infected and then immediately treated with a single dose of 500 μg/kg ivermectin (group infected + IVM, n = 20) or were not infected and treated with PBS (control group, n = 16). Five days after infection/treatment, the mice were euthanized and the tissues were sampled to assess their general health status and infection levels. Overall, the results demonstrated that viral infection induced typical MHV-caused disease, with the livers showing severe hepatocellular necrosis surrounded by a severe lymphoplasmacytic inflammatory infiltration associated with a high hepatic viral load (52,158 AU), while mice treated with ivermectin showed a better health status with a lower viral load (23,192 AU; p < 0.05), with only a few having histopathological liver damage (p < 0.05). No significant differences were found between the group infected + IVM and control group mice (P = NS). Furthermore, serum transaminase levels (aspartate aminotransferase and alanine aminotransferase) were significantly lower in the treated mice than in the infected animals. In conclusion, ivermectin diminished the MHV viral load and disease in the mice, being a useful model for further understanding this therapy against coronavirus diseases. |
| dc.format.extent.es.fl_str_mv | 12 p |
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| dc.identifier.citation.es.fl_str_mv | Arévalo, A, Pagotto, R, Pórfido Barayoli, J, Daghero Villanueva, H, Segovia, M, Yamasaki, K, Varela Cruces, M, Hill, M, Verdes García, J, Duhalde Vega, M, Bollati-Fogolín, M y Crispo, M. Ivermectin reduces in vivo coronavirus infection in a mouse experimental model. Scientific Reports. [en línea] 2021, 11(7132), 1-12 |
| dc.identifier.doi.none.fl_str_mv | https://doi.org/10.1038/s41598-021-86679-0 |
| dc.identifier.uri.none.fl_str_mv | https://hdl.handle.net/20.500.12008/48337 |
| dc.language.iso.none.fl_str_mv | en eng |
| dc.relation.none.fl_str_mv | Scientific Reports, 2021, 11(7132), 1-12 |
| dc.rights.license.none.fl_str_mv | Licencia Creative Commons Atribución (CC - By 4.0) |
| dc.rights.none.fl_str_mv | info:eu-repo/semantics/openAccess |
| dc.source.none.fl_str_mv | reponame:COLIBRI instname:Universidad de la República instacron:Universidad de la República |
| dc.subject.other.es.fl_str_mv | INFECCION EXPERIMENTAL RATONES IVERMECTINA CORONAVIRUS CAUSANTE DEL SINDROME RESPIRATORIO AGUDO SEVERO TERAPIA |
| dc.title.none.fl_str_mv | Ivermectin reduces in vivo coronavirus infection in a mouse experimental model |
| dc.type.es.fl_str_mv | Artículo |
| dc.type.none.fl_str_mv | info:eu-repo/semantics/article |
| dc.type.version.none.fl_str_mv | info:eu-repo/semantics/publishedVersion |
| description | The objective of this study was to test the effectiveness of ivermectin for the treatment of mouse hepatitis virus (MHV), a type 2 family RNA coronavirus similar to SARS-CoV-2. Female BALB/cJ mice were infected with 6,000 PFU of MHV-A59 (group infected, n = 20) or infected and then immediately treated with a single dose of 500 μg/kg ivermectin (group infected + IVM, n = 20) or were not infected and treated with PBS (control group, n = 16). Five days after infection/treatment, the mice were euthanized and the tissues were sampled to assess their general health status and infection levels. Overall, the results demonstrated that viral infection induced typical MHV-caused disease, with the livers showing severe hepatocellular necrosis surrounded by a severe lymphoplasmacytic inflammatory infiltration associated with a high hepatic viral load (52,158 AU), while mice treated with ivermectin showed a better health status with a lower viral load (23,192 AU; p < 0.05), with only a few having histopathological liver damage (p < 0.05). No significant differences were found between the group infected + IVM and control group mice (P = NS). Furthermore, serum transaminase levels (aspartate aminotransferase and alanine aminotransferase) were significantly lower in the treated mice than in the infected animals. In conclusion, ivermectin diminished the MHV viral load and disease in the mice, being a useful model for further understanding this therapy against coronavirus diseases. |
| eu_rights_str_mv | openAccess |
| format | article |
| id | COLIBRI_ebc1ac37fdd61c399d37636b18a430bb |
| identifier_str_mv | Arévalo, A, Pagotto, R, Pórfido Barayoli, J, Daghero Villanueva, H, Segovia, M, Yamasaki, K, Varela Cruces, M, Hill, M, Verdes García, J, Duhalde Vega, M, Bollati-Fogolín, M y Crispo, M. Ivermectin reduces in vivo coronavirus infection in a mouse experimental model. Scientific Reports. [en línea] 2021, 11(7132), 1-12 |
| instacron_str | Universidad de la República |
| institution | Universidad de la República |
| instname_str | Universidad de la República |
| language | eng |
| language_invalid_str_mv | en |
| network_acronym_str | COLIBRI |
| network_name_str | COLIBRI |
| oai_identifier_str | oai:colibri.udelar.edu.uy:20.500.12008/48337 |
| publishDate | 2021 |
| reponame_str | COLIBRI |
| repository.mail.fl_str_mv | karina.camps@seciu.edu.uy |
| repository.name.fl_str_mv | COLIBRI - Universidad de la República |
| repository_id_str | 4771 |
| rights_invalid_str_mv | Licencia Creative Commons Atribución (CC - By 4.0) |
| spelling | Arévalo Ana Paula, Institut Pasteur de Montevideo (Uruguay). Transgenic and Experimental Animal UnitPagotto Romina, Institut Pasteur de Montevideo (Uruguay). Cell Biology UnitPórfido Barayoli Jorge Luis, Institut Pasteur de Montevideo (Uruguay). Transgenic and Experimental Animal Unit / Institut Pasteur de Montevideo (Uruguay). Worm Biology Laboratory / Universidad de la República (Uruguay). Faculty of Chemistry. Department of BiosciencesDaghero Villanueva Hellen, Institut Pasteur de Montevideo (Uruguay). Cell Biology UnitSegovia Mercedes, Institut Pasteur de Montevideo (Uruguay). Laboratory of Immunoregulation and Inflammation / Universidad de la República (Uruguay). Faculty of Medicine. Immunobiology DepartmentYamasaki Kanji, Universidad de la República (Uruguay). Veterinary Faculty. Department of Pathobiology. Pathology UnitVarela Cruces María Belén, Universidad de la República (Uruguay). Veterinary Faculty. Department of Pathobiology. Pathology UnitHill Marcelo, Institut Pasteur de Montevideo (Uruguay). Laboratory of Immunoregulation and Inflammation / Universidad de la República (Uruguay). Faculty of Medicine. Immunobiology DepartmentVerdes García José Manuel, Universidad de la República (Uruguay). Veterinary Faculty. Department of Pathobiology. Pathology UnitDuhalde Vega Maite, Institut Pasteur de Montevideo (Uruguay). Laboratory of Immunoregulation and Inflammation / University of Buenos Aires (Buenos Aires, Argentina). School of Pharmacy and Biochemistry. Institute of Biological Chemistry and Chemical Physics (UBA‑CONICET)Bollati-Fogolín Mariela, Institut Pasteur de Montevideo (Uruguay). Cell Biology UnitCrispo Martina, Institut Pasteur de Montevideo (Uruguay). Transgenic and Experimental Animal Unit2025-02-11T15:26:47Z2025-02-11T15:26:47Z2021Arévalo, A, Pagotto, R, Pórfido Barayoli, J, Daghero Villanueva, H, Segovia, M, Yamasaki, K, Varela Cruces, M, Hill, M, Verdes García, J, Duhalde Vega, M, Bollati-Fogolín, M y Crispo, M. Ivermectin reduces in vivo coronavirus infection in a mouse experimental model. Scientific Reports. [en línea] 2021, 11(7132), 1-12https://hdl.handle.net/20.500.12008/48337https://doi.org/10.1038/s41598-021-86679-0The objective of this study was to test the effectiveness of ivermectin for the treatment of mouse hepatitis virus (MHV), a type 2 family RNA coronavirus similar to SARS-CoV-2. Female BALB/cJ mice were infected with 6,000 PFU of MHV-A59 (group infected, n = 20) or infected and then immediately treated with a single dose of 500 μg/kg ivermectin (group infected + IVM, n = 20) or were not infected and treated with PBS (control group, n = 16). Five days after infection/treatment, the mice were euthanized and the tissues were sampled to assess their general health status and infection levels. Overall, the results demonstrated that viral infection induced typical MHV-caused disease, with the livers showing severe hepatocellular necrosis surrounded by a severe lymphoplasmacytic inflammatory infiltration associated with a high hepatic viral load (52,158 AU), while mice treated with ivermectin showed a better health status with a lower viral load (23,192 AU; p < 0.05), with only a few having histopathological liver damage (p < 0.05). No significant differences were found between the group infected + IVM and control group mice (P = NS). Furthermore, serum transaminase levels (aspartate aminotransferase and alanine aminotransferase) were significantly lower in the treated mice than in the infected animals. In conclusion, ivermectin diminished the MHV viral load and disease in the mice, being a useful model for further understanding this therapy against coronavirus diseases.Submitted by García Alastra Leticia (lgarcia@fvet.edu.uy) on 2025-02-11T15:26:47Z No. of bitstreams: 2 license_rdf: 24251 bytes, checksum: 71ed42ef0a0b648670f707320be37b90 (MD5) V6.pdf: 1698076 bytes, checksum: b1fe1fffbd9fb5764a432580de4da484 (MD5)Made available in DSpace by García Alastra Leticia (lgarcia@fvet.edu.uy) on 2025-02-11T15:26:47Z (GMT). No. of bitstreams: 2 license_rdf: 24251 bytes, checksum: 71ed42ef0a0b648670f707320be37b90 (MD5) V6.pdf: 1698076 bytes, checksum: b1fe1fffbd9fb5764a432580de4da484 (MD5) Previous issue date: 202112 papplication/pdfenengScientific Reports, 2021, 11(7132), 1-12Las obras depositadas en el Repositorio se rigen por la Ordenanza de los Derechos de la Propiedad Intelectual de la Universidad de la República.(Res. Nº 91 de C.D.C. de 8/III/1994 – D.O. 7/IV/1994) y por la Ordenanza del Repositorio Abierto de la Universidad de la República (Res. Nº 16 de C.D.C. de 07/10/2014)info:eu-repo/semantics/openAccessLicencia Creative Commons Atribución (CC - By 4.0)INFECCION EXPERIMENTALRATONESIVERMECTINACORONAVIRUS CAUSANTE DEL SINDROME RESPIRATORIO AGUDO SEVEROTERAPIAIvermectin reduces in vivo coronavirus infection in a mouse experimental modelArtículoinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionreponame:COLIBRIinstname:Universidad de la Repúblicainstacron:Universidad de la RepúblicaArévalo, Ana PaulaPagotto, RominaPórfido Barayoli, Jorge LuisDaghero Villanueva, HellenSegovia, MercedesYamasaki, KanjiVarela Cruces, María BelénHill, MarceloVerdes García, José ManuelDuhalde Vega, MaiteBollati-Fogolín, MarielaCrispo, MartinaLICENSElicense.txtlicense.txttext/plain; charset=utf-84267http://localhost:8080/xmlui/bitstream/20.500.12008/48337/5/license.txt6429389a7df7277b72b7924fdc7d47a9MD55CC-LICENSElicense_urllicense_urltext/plain; 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- Universidad de la Repúblicafalse |
| spellingShingle | Ivermectin reduces in vivo coronavirus infection in a mouse experimental model Arévalo, Ana Paula INFECCION EXPERIMENTAL RATONES IVERMECTINA CORONAVIRUS CAUSANTE DEL SINDROME RESPIRATORIO AGUDO SEVERO TERAPIA |
| status_str | publishedVersion |
| title | Ivermectin reduces in vivo coronavirus infection in a mouse experimental model |
| title_full | Ivermectin reduces in vivo coronavirus infection in a mouse experimental model |
| title_fullStr | Ivermectin reduces in vivo coronavirus infection in a mouse experimental model |
| title_full_unstemmed | Ivermectin reduces in vivo coronavirus infection in a mouse experimental model |
| title_short | Ivermectin reduces in vivo coronavirus infection in a mouse experimental model |
| title_sort | Ivermectin reduces in vivo coronavirus infection in a mouse experimental model |
| topic | INFECCION EXPERIMENTAL RATONES IVERMECTINA CORONAVIRUS CAUSANTE DEL SINDROME RESPIRATORIO AGUDO SEVERO TERAPIA |
| url | https://hdl.handle.net/20.500.12008/48337 https://doi.org/10.1038/s41598-021-86679-0 |