Identification of Chalcones as Fasciola hepatica Cathepsin L inhibitors using a comprehensive experimental and computational approach
Resumen:
Background: Increased reports of human infections have led fasciolosis, a widespread disease of cattle and sheep caused by the liver flukes Fasciola hepatica and Fasciola gigantica, to be considered an emerging zoonotic disease. Chemotherapy is the main control measure available, and triclabendazole is the preferred drug since is effective against both juvenile and mature parasites. However, resistance to triclabendazole has been reported in several countries urging the search of new chemical entities and target molecules to control fluke infections. Methodology/Principle Findings: We searched a library of forty flavonoid derivatives for inhibitors of key stage specific Fasciola hepatica cysteine proteases (FhCL3 and FhCL1). Chalcones substituted with phenyl and naphtyl groups emerged as good cathepsin L inhibitors, interacting more frequently with two putative binding sites within the active site cleft of the enzymes. One of the compounds, C34, tightly bounds to juvenile specific FhCL3 with an IC50 of 5.6 μM. We demonstrated that C34 is a slow-reversible inhibitor that interacts with the Cys-His catalytic dyad and key S2 and S3 pocket residues, determinants of the substrate specificity of this family of cysteine proteases. Interestingly, C34 induces a reduction in NEJ ability to migrate through the gut wall and a loss of motility phenotype that leads to NEJ death within a week in vitro, while it is not cytotoxic to bovine cells. Conclusions/Significance: Up to date there are no reports of in vitro screening for non-peptidic inhibitors of Fasciola hepatica cathepsins, while in general these are considered as the best strategy for in vivo inhibition. We have identified chalcones as novel inhibitors of the two main Cathepsins secreted by juvenile and adult liver flukes. Interestingly, one compound (C34) is highly active towards the juvenile enzyme reducing larval ability to penetrate the gut wall and decreasing NEJ´s viability in vitro. These findings open new avenues for the development of novel agents to control fluke infection and possibly other helminthic diseases.
2016 | |
Fasciolosis Zoonosis Chalcones Fasciola Hepatica |
|
Inglés | |
Universidad de la República | |
COLIBRI | |
https://hdl.handle.net/20.500.12008/22414 | |
Acceso abierto | |
Licencia Creative Commons Atribución (CC - By 4.0) |
_version_ | 1807522781600940032 |
---|---|
author | Ferraro, Florencia |
author2 | Merlino Mellognio, Alicia Beatriz Dell'Oca Runco, Nicolás Gil, Jorge Tort, José F. González, Mercedes Cerecetto, Hugo Cabrera Cedrés, Mauricio Andrés Corvo, Ileana |
author2_role | author author author author author author author author |
author_facet | Ferraro, Florencia Merlino Mellognio, Alicia Beatriz Dell'Oca Runco, Nicolás Gil, Jorge Tort, José F. González, Mercedes Cerecetto, Hugo Cabrera Cedrés, Mauricio Andrés Corvo, Ileana |
author_role | author |
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collection | COLIBRI |
dc.contributor.filiacion.none.fl_str_mv | Ferraro Florencia, Universidad de la República (Uruguay). Facultad de Ciencias. Instituto de Química Biológica Merlino Mellognio Alicia Beatriz, Universidad de la República (Uruguay). Facultad de Ciencias. Instituto de Química Biológica Dell'Oca Runco Nicolás, Universidad de la República (Uruguay). Facultad de Medicina Gil Jorge, Universidad de la República (Uruguay). Facultad de Veterinaria Tort José F., Universidad de la República (Uruguay). Facultad de Medicina González Mercedes, Universidad de la República (Uruguay). Facultad de Ciencias. Instituto de Química Biológica Cerecetto Hugo, Universidad de la República (Uruguay). Facultad de Ciencias. Centro de Investigaciones Nucleares Cabrera Cedrés Mauricio Andrés, Universidad de la República (Uruguay). Facultad de Ciencias. Instituto de Química Biológica Corvo Ileana, Universidad de la República (Uruguay). Facultad de Medicina |
dc.creator.none.fl_str_mv | Ferraro, Florencia Merlino Mellognio, Alicia Beatriz Dell'Oca Runco, Nicolás Gil, Jorge Tort, José F. González, Mercedes Cerecetto, Hugo Cabrera Cedrés, Mauricio Andrés Corvo, Ileana |
dc.date.accessioned.none.fl_str_mv | 2019-11-18T16:19:01Z |
dc.date.available.none.fl_str_mv | 2019-11-18T16:19:01Z |
dc.date.issued.none.fl_str_mv | 2016 |
dc.description.abstract.none.fl_txt_mv | Background: Increased reports of human infections have led fasciolosis, a widespread disease of cattle and sheep caused by the liver flukes Fasciola hepatica and Fasciola gigantica, to be considered an emerging zoonotic disease. Chemotherapy is the main control measure available, and triclabendazole is the preferred drug since is effective against both juvenile and mature parasites. However, resistance to triclabendazole has been reported in several countries urging the search of new chemical entities and target molecules to control fluke infections. Methodology/Principle Findings: We searched a library of forty flavonoid derivatives for inhibitors of key stage specific Fasciola hepatica cysteine proteases (FhCL3 and FhCL1). Chalcones substituted with phenyl and naphtyl groups emerged as good cathepsin L inhibitors, interacting more frequently with two putative binding sites within the active site cleft of the enzymes. One of the compounds, C34, tightly bounds to juvenile specific FhCL3 with an IC50 of 5.6 μM. We demonstrated that C34 is a slow-reversible inhibitor that interacts with the Cys-His catalytic dyad and key S2 and S3 pocket residues, determinants of the substrate specificity of this family of cysteine proteases. Interestingly, C34 induces a reduction in NEJ ability to migrate through the gut wall and a loss of motility phenotype that leads to NEJ death within a week in vitro, while it is not cytotoxic to bovine cells. Conclusions/Significance: Up to date there are no reports of in vitro screening for non-peptidic inhibitors of Fasciola hepatica cathepsins, while in general these are considered as the best strategy for in vivo inhibition. We have identified chalcones as novel inhibitors of the two main Cathepsins secreted by juvenile and adult liver flukes. Interestingly, one compound (C34) is highly active towards the juvenile enzyme reducing larval ability to penetrate the gut wall and decreasing NEJ´s viability in vitro. These findings open new avenues for the development of novel agents to control fluke infection and possibly other helminthic diseases. |
dc.format.extent.es.fl_str_mv | 20 h. |
dc.format.mimetype.es.fl_str_mv | application/pdf |
dc.identifier.citation.es.fl_str_mv | Ferraro, F., Merlino Mellognio, A., Dell'Oca Runco, N., y otros. "Identification of Chalcones as Fasciola hepatica Cathepsin L inhibitors using a comprehensive experimental and computational approach" PLoS Neglected Tropical Diseases [en línea]. 2016 10(7): e0004834. doi: 10.1371/journal.pntd.0004834 |
dc.identifier.doi.none.fl_str_mv | 10.1371/journal.pntd.0004834 |
dc.identifier.issn.none.fl_str_mv | 1935-2735 |
dc.identifier.uri.none.fl_str_mv | https://hdl.handle.net/20.500.12008/22414 |
dc.language.iso.none.fl_str_mv | en eng |
dc.publisher.es.fl_str_mv | PLoS |
dc.relation.ispartof.es.fl_str_mv | PLoS Neglected Tropical Diseases, 2016 10(7): e0004834 |
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.es.fl_str_mv | Fasciolosis Zoonosis Chalcones Fasciola Hepatica |
dc.title.none.fl_str_mv | Identification of Chalcones as Fasciola hepatica Cathepsin L inhibitors using a comprehensive experimental and computational approach |
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 | Background: Increased reports of human infections have led fasciolosis, a widespread disease of cattle and sheep caused by the liver flukes Fasciola hepatica and Fasciola gigantica, to be considered an emerging zoonotic disease. Chemotherapy is the main control measure available, and triclabendazole is the preferred drug since is effective against both juvenile and mature parasites. However, resistance to triclabendazole has been reported in several countries urging the search of new chemical entities and target molecules to control fluke infections. Methodology/Principle Findings: We searched a library of forty flavonoid derivatives for inhibitors of key stage specific Fasciola hepatica cysteine proteases (FhCL3 and FhCL1). Chalcones substituted with phenyl and naphtyl groups emerged as good cathepsin L inhibitors, interacting more frequently with two putative binding sites within the active site cleft of the enzymes. One of the compounds, C34, tightly bounds to juvenile specific FhCL3 with an IC50 of 5.6 μM. We demonstrated that C34 is a slow-reversible inhibitor that interacts with the Cys-His catalytic dyad and key S2 and S3 pocket residues, determinants of the substrate specificity of this family of cysteine proteases. Interestingly, C34 induces a reduction in NEJ ability to migrate through the gut wall and a loss of motility phenotype that leads to NEJ death within a week in vitro, while it is not cytotoxic to bovine cells. Conclusions/Significance: Up to date there are no reports of in vitro screening for non-peptidic inhibitors of Fasciola hepatica cathepsins, while in general these are considered as the best strategy for in vivo inhibition. We have identified chalcones as novel inhibitors of the two main Cathepsins secreted by juvenile and adult liver flukes. Interestingly, one compound (C34) is highly active towards the juvenile enzyme reducing larval ability to penetrate the gut wall and decreasing NEJ´s viability in vitro. These findings open new avenues for the development of novel agents to control fluke infection and possibly other helminthic diseases. |
eu_rights_str_mv | openAccess |
format | article |
id | COLIBRI_63c5c196b76f2f86731b21e6dc50d995 |
identifier_str_mv | Ferraro, F., Merlino Mellognio, A., Dell'Oca Runco, N., y otros. "Identification of Chalcones as Fasciola hepatica Cathepsin L inhibitors using a comprehensive experimental and computational approach" PLoS Neglected Tropical Diseases [en línea]. 2016 10(7): e0004834. doi: 10.1371/journal.pntd.0004834 1935-2735 10.1371/journal.pntd.0004834 |
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:20.500.12008/22414 |
publishDate | 2016 |
reponame_str | COLIBRI |
repository.mail.fl_str_mv | mabel.seroubian@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 | Ferraro Florencia, Universidad de la República (Uruguay). Facultad de Ciencias. Instituto de Química BiológicaMerlino Mellognio Alicia Beatriz, Universidad de la República (Uruguay). Facultad de Ciencias. Instituto de Química BiológicaDell'Oca Runco Nicolás, Universidad de la República (Uruguay). Facultad de MedicinaGil Jorge, Universidad de la República (Uruguay). Facultad de VeterinariaTort José F., Universidad de la República (Uruguay). Facultad de MedicinaGonzález Mercedes, Universidad de la República (Uruguay). Facultad de Ciencias. Instituto de Química BiológicaCerecetto Hugo, Universidad de la República (Uruguay). Facultad de Ciencias. Centro de Investigaciones NuclearesCabrera Cedrés Mauricio Andrés, Universidad de la República (Uruguay). Facultad de Ciencias. Instituto de Química BiológicaCorvo Ileana, Universidad de la República (Uruguay). Facultad de Medicina2019-11-18T16:19:01Z2019-11-18T16:19:01Z2016Ferraro, F., Merlino Mellognio, A., Dell'Oca Runco, N., y otros. "Identification of Chalcones as Fasciola hepatica Cathepsin L inhibitors using a comprehensive experimental and computational approach" PLoS Neglected Tropical Diseases [en línea]. 2016 10(7): e0004834. doi: 10.1371/journal.pntd.00048341935-2735https://hdl.handle.net/20.500.12008/2241410.1371/journal.pntd.0004834Background: Increased reports of human infections have led fasciolosis, a widespread disease of cattle and sheep caused by the liver flukes Fasciola hepatica and Fasciola gigantica, to be considered an emerging zoonotic disease. Chemotherapy is the main control measure available, and triclabendazole is the preferred drug since is effective against both juvenile and mature parasites. However, resistance to triclabendazole has been reported in several countries urging the search of new chemical entities and target molecules to control fluke infections. Methodology/Principle Findings: We searched a library of forty flavonoid derivatives for inhibitors of key stage specific Fasciola hepatica cysteine proteases (FhCL3 and FhCL1). Chalcones substituted with phenyl and naphtyl groups emerged as good cathepsin L inhibitors, interacting more frequently with two putative binding sites within the active site cleft of the enzymes. One of the compounds, C34, tightly bounds to juvenile specific FhCL3 with an IC50 of 5.6 μM. We demonstrated that C34 is a slow-reversible inhibitor that interacts with the Cys-His catalytic dyad and key S2 and S3 pocket residues, determinants of the substrate specificity of this family of cysteine proteases. Interestingly, C34 induces a reduction in NEJ ability to migrate through the gut wall and a loss of motility phenotype that leads to NEJ death within a week in vitro, while it is not cytotoxic to bovine cells. Conclusions/Significance: Up to date there are no reports of in vitro screening for non-peptidic inhibitors of Fasciola hepatica cathepsins, while in general these are considered as the best strategy for in vivo inhibition. We have identified chalcones as novel inhibitors of the two main Cathepsins secreted by juvenile and adult liver flukes. Interestingly, one compound (C34) is highly active towards the juvenile enzyme reducing larval ability to penetrate the gut wall and decreasing NEJ´s viability in vitro. These findings open new avenues for the development of novel agents to control fluke infection and possibly other helminthic diseases.Submitted by Faget Cecilia (lfaget@fcien.edu.uy) on 2019-11-18T14:25:46Z No. of bitstreams: 2 license_rdf: 19874 bytes, checksum: 38cb62ef53e6f513db2fb7e337df6485 (MD5) 101371journalpntd0004834.pdf: 5486782 bytes, checksum: 0ee90b36cfbb7b08d047710bd6b183b0 (MD5)Approved for entry into archive by Faget Cecilia (lfaget@fcien.edu.uy) on 2019-11-18T15:32:09Z (GMT) No. of bitstreams: 2 license_rdf: 19874 bytes, checksum: 38cb62ef53e6f513db2fb7e337df6485 (MD5) 101371journalpntd0004834.pdf: 5486782 bytes, checksum: 0ee90b36cfbb7b08d047710bd6b183b0 (MD5)Made available in DSpace on 2019-11-18T16:19:01Z (GMT). No. of bitstreams: 2 license_rdf: 19874 bytes, checksum: 38cb62ef53e6f513db2fb7e337df6485 (MD5) 101371journalpntd0004834.pdf: 5486782 bytes, checksum: 0ee90b36cfbb7b08d047710bd6b183b0 (MD5) Previous issue date: 201620 h.application/pdfenengPLoSPLoS Neglected Tropical Diseases, 2016 10(7): e0004834Las 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)FasciolosisZoonosisChalconesFasciola HepaticaIdentification of Chalcones as Fasciola hepatica Cathepsin L inhibitors using a comprehensive experimental and computational approachArtículoinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionreponame:COLIBRIinstname:Universidad de la Repúblicainstacron:Universidad de la RepúblicaFerraro, FlorenciaMerlino Mellognio, Alicia BeatrizDell'Oca Runco, NicolásGil, JorgeTort, José F.González, MercedesCerecetto, HugoCabrera Cedrés, Mauricio AndrésCorvo, IleanaLICENSElicense.txtlicense.txttext/plain; charset=utf-84267http://localhost:8080/xmlui/bitstream/20.500.12008/22414/5/license.txt6429389a7df7277b72b7924fdc7d47a9MD55CC-LICENSElicense_urllicense_urltext/plain; charset=utf-844http://localhost:8080/xmlui/bitstream/20.500.12008/22414/2/license_urla0ebbeafb9d2ec7cbb19d7137ebc392cMD52license_textlicense_texttext/html; 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- Universidad de la Repúblicafalse |
spellingShingle | Identification of Chalcones as Fasciola hepatica Cathepsin L inhibitors using a comprehensive experimental and computational approach Ferraro, Florencia Fasciolosis Zoonosis Chalcones Fasciola Hepatica |
status_str | publishedVersion |
title | Identification of Chalcones as Fasciola hepatica Cathepsin L inhibitors using a comprehensive experimental and computational approach |
title_full | Identification of Chalcones as Fasciola hepatica Cathepsin L inhibitors using a comprehensive experimental and computational approach |
title_fullStr | Identification of Chalcones as Fasciola hepatica Cathepsin L inhibitors using a comprehensive experimental and computational approach |
title_full_unstemmed | Identification of Chalcones as Fasciola hepatica Cathepsin L inhibitors using a comprehensive experimental and computational approach |
title_short | Identification of Chalcones as Fasciola hepatica Cathepsin L inhibitors using a comprehensive experimental and computational approach |
title_sort | Identification of Chalcones as Fasciola hepatica Cathepsin L inhibitors using a comprehensive experimental and computational approach |
topic | Fasciolosis Zoonosis Chalcones Fasciola Hepatica |
url | https://hdl.handle.net/20.500.12008/22414 |