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Triclabendazole (Anthelmintic Drug) Effects on the Excretory- Secretory Proteome of Fasciola hepatica in Two Dimension Electrophoresis Gel

BACKGROUND: The aim of this study was to evaluate the protein spots of excretory - secretory products of Fasciola hepatica using two dimension electrophoresis method in the presence and absence of triclabendazole drug which can be considered to detect the target protein of the drug. METHODS: F. hepa...

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Autores principales: FARIDI, Ashkan, FARAHNAK, Ali, GOLMOHAMMADI, Taghi, ESHRAGHIAN, Mohammadreza, SHARIFI, Yosef, MOLAEI RAD, Mohammadbagher
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4386040/
https://www.ncbi.nlm.nih.gov/pubmed/25848386
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author FARIDI, Ashkan
FARAHNAK, Ali
GOLMOHAMMADI, Taghi
ESHRAGHIAN, Mohammadreza
SHARIFI, Yosef
MOLAEI RAD, Mohammadbagher
author_facet FARIDI, Ashkan
FARAHNAK, Ali
GOLMOHAMMADI, Taghi
ESHRAGHIAN, Mohammadreza
SHARIFI, Yosef
MOLAEI RAD, Mohammadbagher
author_sort FARIDI, Ashkan
collection PubMed
description BACKGROUND: The aim of this study was to evaluate the protein spots of excretory - secretory products of Fasciola hepatica using two dimension electrophoresis method in the presence and absence of triclabendazole drug which can be considered to detect the target protein of the drug. METHODS: F. hepatica parasites were collected from infected cattle livers, divided in two groups and cultivated in RPMI 1640 medium. First group was treated with triclabendazole (TCBZ) and second group considered as control. The excretory-secretory (ES) products of each group were separated and total protein determined by Bradford method. To provide proteome spots, the ES proteins were precipitated and two dimension electrophoresis (2-DE) gel prepared. Protein amounts of two groups were compared using the statistical t-test and protein spots from 2-DE in test and control groups were also statistically analyzed. The protein spots of gels were identified by using protein database. RESULTS: The t-test showed a significant increase of total proteins in treated group (P<0.5). The protein spots count in the control group was less than test group however statistically not significant (p>0.05). Cathepsin L- protein (MW 36.7 pH 5.34), 14-3-3 epsilon 2 isoform (MW 28.2 pH 5.36), Cathepsin L1D (MW 36.5 pH 5.8) and Cathepsin L1D (MW 36.6 pH 6.26) were identified in test group. CONCLUSION: It seems that, these results can be considered to determine the proteins which the drug acts as a target on them.
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spelling pubmed-43860402015-04-06 Triclabendazole (Anthelmintic Drug) Effects on the Excretory- Secretory Proteome of Fasciola hepatica in Two Dimension Electrophoresis Gel FARIDI, Ashkan FARAHNAK, Ali GOLMOHAMMADI, Taghi ESHRAGHIAN, Mohammadreza SHARIFI, Yosef MOLAEI RAD, Mohammadbagher Iran J Parasitol Medical Sciences BACKGROUND: The aim of this study was to evaluate the protein spots of excretory - secretory products of Fasciola hepatica using two dimension electrophoresis method in the presence and absence of triclabendazole drug which can be considered to detect the target protein of the drug. METHODS: F. hepatica parasites were collected from infected cattle livers, divided in two groups and cultivated in RPMI 1640 medium. First group was treated with triclabendazole (TCBZ) and second group considered as control. The excretory-secretory (ES) products of each group were separated and total protein determined by Bradford method. To provide proteome spots, the ES proteins were precipitated and two dimension electrophoresis (2-DE) gel prepared. Protein amounts of two groups were compared using the statistical t-test and protein spots from 2-DE in test and control groups were also statistically analyzed. The protein spots of gels were identified by using protein database. RESULTS: The t-test showed a significant increase of total proteins in treated group (P<0.5). The protein spots count in the control group was less than test group however statistically not significant (p>0.05). Cathepsin L- protein (MW 36.7 pH 5.34), 14-3-3 epsilon 2 isoform (MW 28.2 pH 5.36), Cathepsin L1D (MW 36.5 pH 5.8) and Cathepsin L1D (MW 36.6 pH 6.26) were identified in test group. CONCLUSION: It seems that, these results can be considered to determine the proteins which the drug acts as a target on them. Tehran University of Medical Sciences 2014 /pmc/articles/PMC4386040/ /pubmed/25848386 Text en Copyright: © Iranian Journal of Parasitology & Tehran University of Medical Sciences This work is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly.
spellingShingle Medical Sciences
FARIDI, Ashkan
FARAHNAK, Ali
GOLMOHAMMADI, Taghi
ESHRAGHIAN, Mohammadreza
SHARIFI, Yosef
MOLAEI RAD, Mohammadbagher
Triclabendazole (Anthelmintic Drug) Effects on the Excretory- Secretory Proteome of Fasciola hepatica in Two Dimension Electrophoresis Gel
title Triclabendazole (Anthelmintic Drug) Effects on the Excretory- Secretory Proteome of Fasciola hepatica in Two Dimension Electrophoresis Gel
title_full Triclabendazole (Anthelmintic Drug) Effects on the Excretory- Secretory Proteome of Fasciola hepatica in Two Dimension Electrophoresis Gel
title_fullStr Triclabendazole (Anthelmintic Drug) Effects on the Excretory- Secretory Proteome of Fasciola hepatica in Two Dimension Electrophoresis Gel
title_full_unstemmed Triclabendazole (Anthelmintic Drug) Effects on the Excretory- Secretory Proteome of Fasciola hepatica in Two Dimension Electrophoresis Gel
title_short Triclabendazole (Anthelmintic Drug) Effects on the Excretory- Secretory Proteome of Fasciola hepatica in Two Dimension Electrophoresis Gel
title_sort triclabendazole (anthelmintic drug) effects on the excretory- secretory proteome of fasciola hepatica in two dimension electrophoresis gel
topic Medical Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4386040/
https://www.ncbi.nlm.nih.gov/pubmed/25848386
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