Ivermectin reduces in vivo coronavirus infection in a mouse experimental model

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

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.

Detalles Bibliográficos
2021
INFECCION EXPERIMENTAL
RATONES
IVERMECTINA
CORONAVIRUS CAUSANTE DEL SINDROME RESPIRATORIO AGUDO SEVERO
TERAPIA
Inglés
Universidad de la República
COLIBRI
https://hdl.handle.net/20.500.12008/48337
https://doi.org/10.1038/s41598-021-86679-0
Acceso abierto
Licencia Creative Commons Atribución (CC - By 4.0)
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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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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.
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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
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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
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repository.mail.fl_str_mv karina.camps@seciu.edu.uy
repository.name.fl_str_mv COLIBRI - Universidad de la República
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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