Cellular growth and mitochondrial ultrastructure of leishmania (Viannia) braziliensis promastigotes are affected by the iron chelator 2,2-dipyridyl.

<h4>Background</h4>Iron is an essential element for the survival of microorganisms in vitro and in vivo, acting as a cofactor of several enzymes and playing a critical role in host-parasite relationships. Leishmania (Viannia) braziliensis is a parasite that is widespread in the new world...

Full description

Bibliographic Details
Main Authors: Camila Mesquita-Rodrigues, Rubem F S Menna-Barreto, Leonardo Sabóia-Vahia, Silvia A G Da-Silva, Elen M de Souza, Mariana C Waghabi, Patrícia Cuervo, José B De Jesus
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS Neglected Tropical Diseases
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24147167/pdf/?tool=EBI
_version_ 1828897616015917056
author Camila Mesquita-Rodrigues
Rubem F S Menna-Barreto
Leonardo Sabóia-Vahia
Silvia A G Da-Silva
Elen M de Souza
Mariana C Waghabi
Patrícia Cuervo
José B De Jesus
author_facet Camila Mesquita-Rodrigues
Rubem F S Menna-Barreto
Leonardo Sabóia-Vahia
Silvia A G Da-Silva
Elen M de Souza
Mariana C Waghabi
Patrícia Cuervo
José B De Jesus
author_sort Camila Mesquita-Rodrigues
collection DOAJ
description <h4>Background</h4>Iron is an essential element for the survival of microorganisms in vitro and in vivo, acting as a cofactor of several enzymes and playing a critical role in host-parasite relationships. Leishmania (Viannia) braziliensis is a parasite that is widespread in the new world and considered the major etiological agent of American tegumentary leishmaniasis. Although iron depletion leads to promastigote and amastigote growth inhibition, little is known about the role of iron in the biology of Leishmania. Furthermore, there are no reports regarding the importance of iron for L. (V.) braziliensis.<h4>Methodology/principal findings</h4>In this study, the effect of iron on the growth, ultrastructure and protein expression of L. (V.) braziliensis was analyzed by the use of the chelator 2,2-dipyridyl. Treatment with 2,2-dipyridyl affected parasites' growth in a dose- and time-dependent manner. Multiplication of the parasites was recovered after reinoculation in fresh culture medium. Ultrastructural analysis of treated promastigotes revealed marked mitochondrial swelling with loss of cristae and matrix and the presence of concentric membranar structures inside the organelle. Iron depletion also induced Golgi disruption and intense cytoplasmic vacuolization. Fluorescence-activated cell sorting analysis of tetramethylrhodamine ester-stained parasites showed that 2,2-dipyridyl collapsed the mitochondrial membrane potential. The incubation of parasites with propidium iodide demonstrated that disruption of mitochondrial membrane potential was not associated with plasma membrane permeabilization. TUNEL assays indicated no DNA fragmentation in chelator-treated promastigotes. In addition, two-dimensional electrophoresis showed that treatment with the iron chelator induced up- or down-regulation of proteins involved in metabolism of nucleic acids and coordination of post-translational modifications, without altering their mRNA levels.<h4>Conclusions</h4>Iron chelation leads to a multifactorial response that results in cellular collapse, starting with the interruption of cell proliferation and culminating in marked mitochondrial impairment in some parasites and their subsequent cell death, whereas others may survive and resume proliferating.
first_indexed 2024-12-13T15:00:52Z
format Article
id doaj.art-4f8b482a467246179885ef96018684dd
institution Directory Open Access Journal
issn 1935-2727
1935-2735
language English
last_indexed 2024-12-13T15:00:52Z
publishDate 2013-01-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS Neglected Tropical Diseases
spelling doaj.art-4f8b482a467246179885ef96018684dd2022-12-21T23:41:08ZengPublic Library of Science (PLoS)PLoS Neglected Tropical Diseases1935-27271935-27352013-01-01710e248110.1371/journal.pntd.0002481Cellular growth and mitochondrial ultrastructure of leishmania (Viannia) braziliensis promastigotes are affected by the iron chelator 2,2-dipyridyl.Camila Mesquita-RodriguesRubem F S Menna-BarretoLeonardo Sabóia-VahiaSilvia A G Da-SilvaElen M de SouzaMariana C WaghabiPatrícia CuervoJosé B De Jesus<h4>Background</h4>Iron is an essential element for the survival of microorganisms in vitro and in vivo, acting as a cofactor of several enzymes and playing a critical role in host-parasite relationships. Leishmania (Viannia) braziliensis is a parasite that is widespread in the new world and considered the major etiological agent of American tegumentary leishmaniasis. Although iron depletion leads to promastigote and amastigote growth inhibition, little is known about the role of iron in the biology of Leishmania. Furthermore, there are no reports regarding the importance of iron for L. (V.) braziliensis.<h4>Methodology/principal findings</h4>In this study, the effect of iron on the growth, ultrastructure and protein expression of L. (V.) braziliensis was analyzed by the use of the chelator 2,2-dipyridyl. Treatment with 2,2-dipyridyl affected parasites' growth in a dose- and time-dependent manner. Multiplication of the parasites was recovered after reinoculation in fresh culture medium. Ultrastructural analysis of treated promastigotes revealed marked mitochondrial swelling with loss of cristae and matrix and the presence of concentric membranar structures inside the organelle. Iron depletion also induced Golgi disruption and intense cytoplasmic vacuolization. Fluorescence-activated cell sorting analysis of tetramethylrhodamine ester-stained parasites showed that 2,2-dipyridyl collapsed the mitochondrial membrane potential. The incubation of parasites with propidium iodide demonstrated that disruption of mitochondrial membrane potential was not associated with plasma membrane permeabilization. TUNEL assays indicated no DNA fragmentation in chelator-treated promastigotes. In addition, two-dimensional electrophoresis showed that treatment with the iron chelator induced up- or down-regulation of proteins involved in metabolism of nucleic acids and coordination of post-translational modifications, without altering their mRNA levels.<h4>Conclusions</h4>Iron chelation leads to a multifactorial response that results in cellular collapse, starting with the interruption of cell proliferation and culminating in marked mitochondrial impairment in some parasites and their subsequent cell death, whereas others may survive and resume proliferating.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24147167/pdf/?tool=EBI
spellingShingle Camila Mesquita-Rodrigues
Rubem F S Menna-Barreto
Leonardo Sabóia-Vahia
Silvia A G Da-Silva
Elen M de Souza
Mariana C Waghabi
Patrícia Cuervo
José B De Jesus
Cellular growth and mitochondrial ultrastructure of leishmania (Viannia) braziliensis promastigotes are affected by the iron chelator 2,2-dipyridyl.
PLoS Neglected Tropical Diseases
title Cellular growth and mitochondrial ultrastructure of leishmania (Viannia) braziliensis promastigotes are affected by the iron chelator 2,2-dipyridyl.
title_full Cellular growth and mitochondrial ultrastructure of leishmania (Viannia) braziliensis promastigotes are affected by the iron chelator 2,2-dipyridyl.
title_fullStr Cellular growth and mitochondrial ultrastructure of leishmania (Viannia) braziliensis promastigotes are affected by the iron chelator 2,2-dipyridyl.
title_full_unstemmed Cellular growth and mitochondrial ultrastructure of leishmania (Viannia) braziliensis promastigotes are affected by the iron chelator 2,2-dipyridyl.
title_short Cellular growth and mitochondrial ultrastructure of leishmania (Viannia) braziliensis promastigotes are affected by the iron chelator 2,2-dipyridyl.
title_sort cellular growth and mitochondrial ultrastructure of leishmania viannia braziliensis promastigotes are affected by the iron chelator 2 2 dipyridyl
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24147167/pdf/?tool=EBI
work_keys_str_mv AT camilamesquitarodrigues cellulargrowthandmitochondrialultrastructureofleishmaniavianniabraziliensispromastigotesareaffectedbytheironchelator22dipyridyl
AT rubemfsmennabarreto cellulargrowthandmitochondrialultrastructureofleishmaniavianniabraziliensispromastigotesareaffectedbytheironchelator22dipyridyl
AT leonardosaboiavahia cellulargrowthandmitochondrialultrastructureofleishmaniavianniabraziliensispromastigotesareaffectedbytheironchelator22dipyridyl
AT silviaagdasilva cellulargrowthandmitochondrialultrastructureofleishmaniavianniabraziliensispromastigotesareaffectedbytheironchelator22dipyridyl
AT elenmdesouza cellulargrowthandmitochondrialultrastructureofleishmaniavianniabraziliensispromastigotesareaffectedbytheironchelator22dipyridyl
AT marianacwaghabi cellulargrowthandmitochondrialultrastructureofleishmaniavianniabraziliensispromastigotesareaffectedbytheironchelator22dipyridyl
AT patriciacuervo cellulargrowthandmitochondrialultrastructureofleishmaniavianniabraziliensispromastigotesareaffectedbytheironchelator22dipyridyl
AT josebdejesus cellulargrowthandmitochondrialultrastructureofleishmaniavianniabraziliensispromastigotesareaffectedbytheironchelator22dipyridyl