Cargando…

Parasitic Loads in Tissues of Mice Infected with Trypanosoma cruzi and Treated with AmBisome

BACKGROUND: Chagas disease is one of the most important public health problems and a leading cause of cardiac failure in Latin America. The currently available drugs to treat T. cruzi infection (benznidazole and nifurtimox) are effective in humans when administered during months. AmBisome (liposomal...

Descripción completa

Detalles Bibliográficos
Autores principales: Cencig, Sabrina, Coltel, Nicolas, Truyens, Carine, Carlier, Yves
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3125148/
https://www.ncbi.nlm.nih.gov/pubmed/21738811
http://dx.doi.org/10.1371/journal.pntd.0001216
_version_ 1782207168488931328
author Cencig, Sabrina
Coltel, Nicolas
Truyens, Carine
Carlier, Yves
author_facet Cencig, Sabrina
Coltel, Nicolas
Truyens, Carine
Carlier, Yves
author_sort Cencig, Sabrina
collection PubMed
description BACKGROUND: Chagas disease is one of the most important public health problems and a leading cause of cardiac failure in Latin America. The currently available drugs to treat T. cruzi infection (benznidazole and nifurtimox) are effective in humans when administered during months. AmBisome (liposomal amphotericin B), already shown efficient after administration for some days in human and experimental infection with Leishmania, has been scarcely studied in T. cruzi infection. AIMS: This work investigates the effect of AmBisome treatment, administered in 6 intraperitoneal injections at various times during acute and/or chronic phases of mouse T. cruzi infection, comparing survival rates and parasitic loads in several tissues. METHODOLOGY: Quantitative PCR was used to determine parasitic DNA amounts in tissues. Immunosuppressive treatment with cyclophosphamide was used to investigate residual infection in tissues. FINDINGS: Administration of AmBisome during the acute phase of infection prevented mice from fatal issue. Parasitaemias (microscopic examination) were reduced in acute phase and undetectable in chronic infection. Quantitative PCR analyses showed significant parasite load reductions in heart, liver, spleen, skeletal muscle and adipose tissues in acute as well as in chronic infection. An earlier administration of AmBisome (one day after parasite inoculation) had a better effect in reducing parasite loads in spleen and liver, whereas repetition of treatment in chronic phase enhanced the parasite load reduction in heart and liver. However, whatever the treatment schedule, cyclophosphamide injections boosted infection to parasite amounts comparable to those observed in acutely infected and untreated mice. CONCLUSIONS: Though AmBisome treatment fails to completely cure mice from T. cruzi infection, it impedes mortality and reduces significantly the parasitic loads in most tissues. Such a beneficial effect, obtained by administrating it over a short time, should stimulate studies on using AmBisome in association with other drugs in order to shorten recovery from T. cruzi infection.
format Online
Article
Text
id pubmed-3125148
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-31251482011-07-07 Parasitic Loads in Tissues of Mice Infected with Trypanosoma cruzi and Treated with AmBisome Cencig, Sabrina Coltel, Nicolas Truyens, Carine Carlier, Yves PLoS Negl Trop Dis Research Article BACKGROUND: Chagas disease is one of the most important public health problems and a leading cause of cardiac failure in Latin America. The currently available drugs to treat T. cruzi infection (benznidazole and nifurtimox) are effective in humans when administered during months. AmBisome (liposomal amphotericin B), already shown efficient after administration for some days in human and experimental infection with Leishmania, has been scarcely studied in T. cruzi infection. AIMS: This work investigates the effect of AmBisome treatment, administered in 6 intraperitoneal injections at various times during acute and/or chronic phases of mouse T. cruzi infection, comparing survival rates and parasitic loads in several tissues. METHODOLOGY: Quantitative PCR was used to determine parasitic DNA amounts in tissues. Immunosuppressive treatment with cyclophosphamide was used to investigate residual infection in tissues. FINDINGS: Administration of AmBisome during the acute phase of infection prevented mice from fatal issue. Parasitaemias (microscopic examination) were reduced in acute phase and undetectable in chronic infection. Quantitative PCR analyses showed significant parasite load reductions in heart, liver, spleen, skeletal muscle and adipose tissues in acute as well as in chronic infection. An earlier administration of AmBisome (one day after parasite inoculation) had a better effect in reducing parasite loads in spleen and liver, whereas repetition of treatment in chronic phase enhanced the parasite load reduction in heart and liver. However, whatever the treatment schedule, cyclophosphamide injections boosted infection to parasite amounts comparable to those observed in acutely infected and untreated mice. CONCLUSIONS: Though AmBisome treatment fails to completely cure mice from T. cruzi infection, it impedes mortality and reduces significantly the parasitic loads in most tissues. Such a beneficial effect, obtained by administrating it over a short time, should stimulate studies on using AmBisome in association with other drugs in order to shorten recovery from T. cruzi infection. Public Library of Science 2011-06-28 /pmc/articles/PMC3125148/ /pubmed/21738811 http://dx.doi.org/10.1371/journal.pntd.0001216 Text en Cencig et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Cencig, Sabrina
Coltel, Nicolas
Truyens, Carine
Carlier, Yves
Parasitic Loads in Tissues of Mice Infected with Trypanosoma cruzi and Treated with AmBisome
title Parasitic Loads in Tissues of Mice Infected with Trypanosoma cruzi and Treated with AmBisome
title_full Parasitic Loads in Tissues of Mice Infected with Trypanosoma cruzi and Treated with AmBisome
title_fullStr Parasitic Loads in Tissues of Mice Infected with Trypanosoma cruzi and Treated with AmBisome
title_full_unstemmed Parasitic Loads in Tissues of Mice Infected with Trypanosoma cruzi and Treated with AmBisome
title_short Parasitic Loads in Tissues of Mice Infected with Trypanosoma cruzi and Treated with AmBisome
title_sort parasitic loads in tissues of mice infected with trypanosoma cruzi and treated with ambisome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3125148/
https://www.ncbi.nlm.nih.gov/pubmed/21738811
http://dx.doi.org/10.1371/journal.pntd.0001216
work_keys_str_mv AT cencigsabrina parasiticloadsintissuesofmiceinfectedwithtrypanosomacruziandtreatedwithambisome
AT coltelnicolas parasiticloadsintissuesofmiceinfectedwithtrypanosomacruziandtreatedwithambisome
AT truyenscarine parasiticloadsintissuesofmiceinfectedwithtrypanosomacruziandtreatedwithambisome
AT carlieryves parasiticloadsintissuesofmiceinfectedwithtrypanosomacruziandtreatedwithambisome