Identification of differentially expressed proteins from Leishmania amazonensis associated with the loss of virulence of the parasites.

BACKGROUND: The present study analyzed whether or not the in vitro cultivation for long periods of time of pre-isolated Leishmania amazonensis from lesions of chronically infected BALB/c mice was able to interfere in the parasites' infectivity using in vivo and in vitro experiments. In addition...

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Main Authors: Rubens D M Magalhães, Mariana C Duarte, Eliciane C Mattos, Vivian T Martins, Paula S Lage, Miguel A Chávez-Fumagalli, Daniela P Lage, Daniel Menezes-Souza, Wiliam C B Régis, Maria J Manso Alves, Manuel Soto, Carlos A P Tavares, Ronaldo A P Nagen, Eduardo A F Coelho
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-04-01
Series:PLoS Neglected Tropical Diseases
Online Access:http://europepmc.org/articles/PMC3974679?pdf=render
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spelling doaj-6c8cc82b470a425692b3edab10a2e3802020-11-25T02:07:49ZengPublic Library of Science (PLoS)PLoS Neglected Tropical Diseases1935-27271935-27352014-04-0184e276410.1371/journal.pntd.0002764Identification of differentially expressed proteins from Leishmania amazonensis associated with the loss of virulence of the parasites.Rubens D M MagalhãesMariana C DuarteEliciane C MattosVivian T MartinsPaula S LageMiguel A Chávez-FumagalliDaniela P LageDaniel Menezes-SouzaWiliam C B RégisMaria J Manso AlvesManuel SotoCarlos A P TavaresRonaldo A P NagenEduardo A F CoelhoBACKGROUND: The present study analyzed whether or not the in vitro cultivation for long periods of time of pre-isolated Leishmania amazonensis from lesions of chronically infected BALB/c mice was able to interfere in the parasites' infectivity using in vivo and in vitro experiments. In addition, the proteins that presented a significant decrease or increase in their protein expression content were identified applying a proteomic approach. METHODOLOGY/PRINCIPAL FINDINGS: Parasites were cultured in vitro for 150 days. Aliquots were collected on the day 0 of culture (R0), as well as after ten (R10; 50 days of culture), twenty (R20; 100 days of culture), and thirty (R30; 150 days of culture) passages, and were used to analyze the parasites' in vitro and in vivo infectivity, as well as to perform the proteomic approach. Approximately 837, 967, 935, and 872 spots were found in 2-DE gels prepared from R0, R10, R20, and R30 samples, respectively. A total of 37 spots presented a significant decrease in their intensity of expression, whereas a significant increase in protein content during cultivation could be observed for 19 proteins (both cases >2.0 folds). Some of these identified proteins can be described, such as diagnosis and/or vaccine candidates, while others are involved in the infectivity of Leishmania. It is interesting to note that six proteins, considered hypothetical in Leishmania, showed a significant decrease in their expression and were also identified. CONCLUSIONS/SIGNIFICANCE: The present study contributes to the understanding that the cultivation of parasites over long periods of time may well be related to the possible loss of infectivity of L. amazonensis. The identified proteins that presented a significant decrease in their expression during cultivation, including the hypothetical, may also be related to this loss of parasites' infectivity, and applied in future studies, including vaccine candidates and/or immunotherapeutic targets against leishmaniasis.http://europepmc.org/articles/PMC3974679?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Rubens D M Magalhães
Mariana C Duarte
Eliciane C Mattos
Vivian T Martins
Paula S Lage
Miguel A Chávez-Fumagalli
Daniela P Lage
Daniel Menezes-Souza
Wiliam C B Régis
Maria J Manso Alves
Manuel Soto
Carlos A P Tavares
Ronaldo A P Nagen
Eduardo A F Coelho
spellingShingle Rubens D M Magalhães
Mariana C Duarte
Eliciane C Mattos
Vivian T Martins
Paula S Lage
Miguel A Chávez-Fumagalli
Daniela P Lage
Daniel Menezes-Souza
Wiliam C B Régis
Maria J Manso Alves
Manuel Soto
Carlos A P Tavares
Ronaldo A P Nagen
Eduardo A F Coelho
Identification of differentially expressed proteins from Leishmania amazonensis associated with the loss of virulence of the parasites.
PLoS Neglected Tropical Diseases
author_facet Rubens D M Magalhães
Mariana C Duarte
Eliciane C Mattos
Vivian T Martins
Paula S Lage
Miguel A Chávez-Fumagalli
Daniela P Lage
Daniel Menezes-Souza
Wiliam C B Régis
Maria J Manso Alves
Manuel Soto
Carlos A P Tavares
Ronaldo A P Nagen
Eduardo A F Coelho
author_sort Rubens D M Magalhães
title Identification of differentially expressed proteins from Leishmania amazonensis associated with the loss of virulence of the parasites.
title_short Identification of differentially expressed proteins from Leishmania amazonensis associated with the loss of virulence of the parasites.
title_full Identification of differentially expressed proteins from Leishmania amazonensis associated with the loss of virulence of the parasites.
title_fullStr Identification of differentially expressed proteins from Leishmania amazonensis associated with the loss of virulence of the parasites.
title_full_unstemmed Identification of differentially expressed proteins from Leishmania amazonensis associated with the loss of virulence of the parasites.
title_sort identification of differentially expressed proteins from leishmania amazonensis associated with the loss of virulence of the parasites.
publisher Public Library of Science (PLoS)
series PLoS Neglected Tropical Diseases
issn 1935-2727
1935-2735
publishDate 2014-04-01
description BACKGROUND: The present study analyzed whether or not the in vitro cultivation for long periods of time of pre-isolated Leishmania amazonensis from lesions of chronically infected BALB/c mice was able to interfere in the parasites' infectivity using in vivo and in vitro experiments. In addition, the proteins that presented a significant decrease or increase in their protein expression content were identified applying a proteomic approach. METHODOLOGY/PRINCIPAL FINDINGS: Parasites were cultured in vitro for 150 days. Aliquots were collected on the day 0 of culture (R0), as well as after ten (R10; 50 days of culture), twenty (R20; 100 days of culture), and thirty (R30; 150 days of culture) passages, and were used to analyze the parasites' in vitro and in vivo infectivity, as well as to perform the proteomic approach. Approximately 837, 967, 935, and 872 spots were found in 2-DE gels prepared from R0, R10, R20, and R30 samples, respectively. A total of 37 spots presented a significant decrease in their intensity of expression, whereas a significant increase in protein content during cultivation could be observed for 19 proteins (both cases >2.0 folds). Some of these identified proteins can be described, such as diagnosis and/or vaccine candidates, while others are involved in the infectivity of Leishmania. It is interesting to note that six proteins, considered hypothetical in Leishmania, showed a significant decrease in their expression and were also identified. CONCLUSIONS/SIGNIFICANCE: The present study contributes to the understanding that the cultivation of parasites over long periods of time may well be related to the possible loss of infectivity of L. amazonensis. The identified proteins that presented a significant decrease in their expression during cultivation, including the hypothetical, may also be related to this loss of parasites' infectivity, and applied in future studies, including vaccine candidates and/or immunotherapeutic targets against leishmaniasis.
url http://europepmc.org/articles/PMC3974679?pdf=render
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