Combination With Tomatidine Improves the Potency of Posaconazole Against Trypanosoma cruzi

Azoles such as posaconazole (Posa) are highly potent against Trypanosoma cruzi. However, when tested in chronic Chagas disease patients, a high rate of relapse after Posa treatment was observed. It appears that inhibition of T. cruzi cytochrome CYP51, the target of azoles, does not deliver sterile c...

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Main Authors: Marianne Rocha-Hasler, Gabriel Melo de Oliveira, Aline Nefertiti da Gama, Ludmila Ferreira de Almeida Fiuza, Anna Frieda Fesser, Monica Cal, Romina Rocchetti, Raiza Brandão Peres, Xue Li Guan, Marcel Kaiser, Maria de Nazaré Correia Soeiro, Pascal Mäser
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-03-01
Series:Frontiers in Cellular and Infection Microbiology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fcimb.2021.617917/full
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language English
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author Marianne Rocha-Hasler
Marianne Rocha-Hasler
Marianne Rocha-Hasler
Gabriel Melo de Oliveira
Aline Nefertiti da Gama
Ludmila Ferreira de Almeida Fiuza
Anna Frieda Fesser
Anna Frieda Fesser
Monica Cal
Monica Cal
Romina Rocchetti
Romina Rocchetti
Raiza Brandão Peres
Xue Li Guan
Marcel Kaiser
Marcel Kaiser
Maria de Nazaré Correia Soeiro
Pascal Mäser
Pascal Mäser
spellingShingle Marianne Rocha-Hasler
Marianne Rocha-Hasler
Marianne Rocha-Hasler
Gabriel Melo de Oliveira
Aline Nefertiti da Gama
Ludmila Ferreira de Almeida Fiuza
Anna Frieda Fesser
Anna Frieda Fesser
Monica Cal
Monica Cal
Romina Rocchetti
Romina Rocchetti
Raiza Brandão Peres
Xue Li Guan
Marcel Kaiser
Marcel Kaiser
Maria de Nazaré Correia Soeiro
Pascal Mäser
Pascal Mäser
Combination With Tomatidine Improves the Potency of Posaconazole Against Trypanosoma cruzi
Frontiers in Cellular and Infection Microbiology
Chagas disease
tomatidine hydrochloride
drug combination
T. cruzi
lipid biosynthesis inhibitor
author_facet Marianne Rocha-Hasler
Marianne Rocha-Hasler
Marianne Rocha-Hasler
Gabriel Melo de Oliveira
Aline Nefertiti da Gama
Ludmila Ferreira de Almeida Fiuza
Anna Frieda Fesser
Anna Frieda Fesser
Monica Cal
Monica Cal
Romina Rocchetti
Romina Rocchetti
Raiza Brandão Peres
Xue Li Guan
Marcel Kaiser
Marcel Kaiser
Maria de Nazaré Correia Soeiro
Pascal Mäser
Pascal Mäser
author_sort Marianne Rocha-Hasler
title Combination With Tomatidine Improves the Potency of Posaconazole Against Trypanosoma cruzi
title_short Combination With Tomatidine Improves the Potency of Posaconazole Against Trypanosoma cruzi
title_full Combination With Tomatidine Improves the Potency of Posaconazole Against Trypanosoma cruzi
title_fullStr Combination With Tomatidine Improves the Potency of Posaconazole Against Trypanosoma cruzi
title_full_unstemmed Combination With Tomatidine Improves the Potency of Posaconazole Against Trypanosoma cruzi
title_sort combination with tomatidine improves the potency of posaconazole against trypanosoma cruzi
publisher Frontiers Media S.A.
series Frontiers in Cellular and Infection Microbiology
issn 2235-2988
publishDate 2021-03-01
description Azoles such as posaconazole (Posa) are highly potent against Trypanosoma cruzi. However, when tested in chronic Chagas disease patients, a high rate of relapse after Posa treatment was observed. It appears that inhibition of T. cruzi cytochrome CYP51, the target of azoles, does not deliver sterile cure in monotherapy. Looking for suitable combination partners of azoles, we have selected a set of inhibitors of sterol and sphingolipid biosynthetic enzymes. A small-scale phenotypic screening was conducted in vitro against the proliferative forms of T. cruzi, extracellular epimastigotes and intracellular amastigotes. Against the intracellular, clinically relevant forms, four out of 15 tested compounds presented higher or equal activity as benznidazole (Bz), with EC50 values ≤2.2 μM. Ro48-8071, an inhibitor of lanosterol synthase (ERG7), and the steroidal alkaloid tomatidine (TH), an inhibitor of C-24 sterol methyltransferase (ERG6), exhibited the highest potency and selectivity indices (SI = 12 and 115, respectively). Both were directed to combinatory assays using fixed-ratio protocols with Posa, Bz, and fexinidazole. The combination of TH with Posa displayed a synergistic profile against amastigotes, with a mean ΣFICI value of 0.2. In vivo assays using an acute mouse model of T. cruzi infection demonstrated lack of antiparasitic activity of TH alone in doses ranging from 0.5 to 5 mg/kg. As observed in vitro, the best combo proportion in vivo was the ratio 3 TH:1 Posa. The combination of Posa at 1.25 mpk plus TH at 3.75 mpk displayed suppression of peak parasitemia of 80% and a survival rate of 60% in the acute infection model, as compared to 20% survival for Posa at 1.25 mpk alone and 40% for Posa at 10 mpk alone. These initial results indicate a potential for the combination of posaconazole with tomatidine against T. cruzi.
topic Chagas disease
tomatidine hydrochloride
drug combination
T. cruzi
lipid biosynthesis inhibitor
url https://www.frontiersin.org/articles/10.3389/fcimb.2021.617917/full
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spelling doaj-ee5ab12cf3d84660be77eec921094bc62021-03-04T08:36:49ZengFrontiers Media S.A.Frontiers in Cellular and Infection Microbiology2235-29882021-03-011110.3389/fcimb.2021.617917617917Combination With Tomatidine Improves the Potency of Posaconazole Against Trypanosoma cruziMarianne Rocha-Hasler0Marianne Rocha-Hasler1Marianne Rocha-Hasler2Gabriel Melo de Oliveira3Aline Nefertiti da Gama4Ludmila Ferreira de Almeida Fiuza5Anna Frieda Fesser6Anna Frieda Fesser7Monica Cal8Monica Cal9Romina Rocchetti10Romina Rocchetti11Raiza Brandão Peres12Xue Li Guan13Marcel Kaiser14Marcel Kaiser15Maria de Nazaré Correia Soeiro16Pascal Mäser17Pascal Mäser18Laboratório de Biologia Celular, Instituto Oswaldo Cruz (IOC/Fiocruz), Pavilhão Cardoso Fontes, Rio de Janeiro, BrazilParasite Chemotherapy Unit, Swiss Tropical and Public Health Institute, Medical Parasitology and Infection Biology, Basel, SwitzerlandUniversity of Basel, Basel, SwitzerlandLaboratório de Biologia Celular, Instituto Oswaldo Cruz (IOC/Fiocruz), Pavilhão Cardoso Fontes, Rio de Janeiro, BrazilLaboratório de Biologia Celular, Instituto Oswaldo Cruz (IOC/Fiocruz), Pavilhão Cardoso Fontes, Rio de Janeiro, BrazilLaboratório de Biologia Celular, Instituto Oswaldo Cruz (IOC/Fiocruz), Pavilhão Cardoso Fontes, Rio de Janeiro, BrazilParasite Chemotherapy Unit, Swiss Tropical and Public Health Institute, Medical Parasitology and Infection Biology, Basel, SwitzerlandUniversity of Basel, Basel, SwitzerlandParasite Chemotherapy Unit, Swiss Tropical and Public Health Institute, Medical Parasitology and Infection Biology, Basel, SwitzerlandUniversity of Basel, Basel, SwitzerlandParasite Chemotherapy Unit, Swiss Tropical and Public Health Institute, Medical Parasitology and Infection Biology, Basel, SwitzerlandUniversity of Basel, Basel, SwitzerlandLaboratório de Biologia Celular, Instituto Oswaldo Cruz (IOC/Fiocruz), Pavilhão Cardoso Fontes, Rio de Janeiro, BrazilSystems Biology of Lipid Metabolism in Human Health and Diseases Laboratory, Lee Kong Chian School of Medicine, Singapore, SingaporeParasite Chemotherapy Unit, Swiss Tropical and Public Health Institute, Medical Parasitology and Infection Biology, Basel, SwitzerlandUniversity of Basel, Basel, SwitzerlandLaboratório de Biologia Celular, Instituto Oswaldo Cruz (IOC/Fiocruz), Pavilhão Cardoso Fontes, Rio de Janeiro, BrazilParasite Chemotherapy Unit, Swiss Tropical and Public Health Institute, Medical Parasitology and Infection Biology, Basel, SwitzerlandUniversity of Basel, Basel, SwitzerlandAzoles such as posaconazole (Posa) are highly potent against Trypanosoma cruzi. However, when tested in chronic Chagas disease patients, a high rate of relapse after Posa treatment was observed. It appears that inhibition of T. cruzi cytochrome CYP51, the target of azoles, does not deliver sterile cure in monotherapy. Looking for suitable combination partners of azoles, we have selected a set of inhibitors of sterol and sphingolipid biosynthetic enzymes. A small-scale phenotypic screening was conducted in vitro against the proliferative forms of T. cruzi, extracellular epimastigotes and intracellular amastigotes. Against the intracellular, clinically relevant forms, four out of 15 tested compounds presented higher or equal activity as benznidazole (Bz), with EC50 values ≤2.2 μM. Ro48-8071, an inhibitor of lanosterol synthase (ERG7), and the steroidal alkaloid tomatidine (TH), an inhibitor of C-24 sterol methyltransferase (ERG6), exhibited the highest potency and selectivity indices (SI = 12 and 115, respectively). Both were directed to combinatory assays using fixed-ratio protocols with Posa, Bz, and fexinidazole. The combination of TH with Posa displayed a synergistic profile against amastigotes, with a mean ΣFICI value of 0.2. In vivo assays using an acute mouse model of T. cruzi infection demonstrated lack of antiparasitic activity of TH alone in doses ranging from 0.5 to 5 mg/kg. As observed in vitro, the best combo proportion in vivo was the ratio 3 TH:1 Posa. The combination of Posa at 1.25 mpk plus TH at 3.75 mpk displayed suppression of peak parasitemia of 80% and a survival rate of 60% in the acute infection model, as compared to 20% survival for Posa at 1.25 mpk alone and 40% for Posa at 10 mpk alone. These initial results indicate a potential for the combination of posaconazole with tomatidine against T. cruzi.https://www.frontiersin.org/articles/10.3389/fcimb.2021.617917/fullChagas diseasetomatidine hydrochloridedrug combinationT. cruzilipid biosynthesis inhibitor