Identification of Chalcones as Fasciola hepatica Cathepsin L inhibitors using a comprehensive experimental and computational approach

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

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.


Detalles Bibliográficos
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)
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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.
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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.
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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
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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 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