Endocytosis and Exocytosis in Leishmania amazonensis Are Modulated by Bromoenol Lactone

In the protozoan pathogen Leishmania, endocytosis, and exocytosis occur mainly in the small area of the flagellar pocket membrane, which makes this parasite an interesting model of strikingly polarized internalization and secretion. Moreover, little is known about vesicle recognition and fusion mech...

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Main Authors: Anne C. S. Fernandes, Deivid C. Soares, Roberta F. C. Neves, Carolina M. Koeller, Norton Heise, Camila M. Adade, Susana Frases, José R. Meyer-Fernandes, Elvira M. Saraiva, Thaïs Souto-Padrón
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-02-01
Series:Frontiers in Cellular and Infection Microbiology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fcimb.2020.00039/full
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author Anne C. S. Fernandes
Anne C. S. Fernandes
Deivid C. Soares
Roberta F. C. Neves
Carolina M. Koeller
Norton Heise
Camila M. Adade
Susana Frases
José R. Meyer-Fernandes
José R. Meyer-Fernandes
Elvira M. Saraiva
Thaïs Souto-Padrón
Thaïs Souto-Padrón
spellingShingle Anne C. S. Fernandes
Anne C. S. Fernandes
Deivid C. Soares
Roberta F. C. Neves
Carolina M. Koeller
Norton Heise
Camila M. Adade
Susana Frases
José R. Meyer-Fernandes
José R. Meyer-Fernandes
Elvira M. Saraiva
Thaïs Souto-Padrón
Thaïs Souto-Padrón
Endocytosis and Exocytosis in Leishmania amazonensis Are Modulated by Bromoenol Lactone
Frontiers in Cellular and Infection Microbiology
Leishmania amazonensis
bromoenol lactone (BEL)
endocytic pathways
exocytic pathways
ultrastructure
calcium-independent phospholipase A2
author_facet Anne C. S. Fernandes
Anne C. S. Fernandes
Deivid C. Soares
Roberta F. C. Neves
Carolina M. Koeller
Norton Heise
Camila M. Adade
Susana Frases
José R. Meyer-Fernandes
José R. Meyer-Fernandes
Elvira M. Saraiva
Thaïs Souto-Padrón
Thaïs Souto-Padrón
author_sort Anne C. S. Fernandes
title Endocytosis and Exocytosis in Leishmania amazonensis Are Modulated by Bromoenol Lactone
title_short Endocytosis and Exocytosis in Leishmania amazonensis Are Modulated by Bromoenol Lactone
title_full Endocytosis and Exocytosis in Leishmania amazonensis Are Modulated by Bromoenol Lactone
title_fullStr Endocytosis and Exocytosis in Leishmania amazonensis Are Modulated by Bromoenol Lactone
title_full_unstemmed Endocytosis and Exocytosis in Leishmania amazonensis Are Modulated by Bromoenol Lactone
title_sort endocytosis and exocytosis in leishmania amazonensis are modulated by bromoenol lactone
publisher Frontiers Media S.A.
series Frontiers in Cellular and Infection Microbiology
issn 2235-2988
publishDate 2020-02-01
description In the protozoan pathogen Leishmania, endocytosis, and exocytosis occur mainly in the small area of the flagellar pocket membrane, which makes this parasite an interesting model of strikingly polarized internalization and secretion. Moreover, little is known about vesicle recognition and fusion mechanisms, which are essential for both endo/exocytosis in this parasite. In other cell types, vesicle fusion events require the activity of phospholipase A2 (PLA2), including Ca2+-independent iPLA2 and soluble, Ca2+-dependent sPLA2. Here, we studied the role of bromoenol lactone (BEL) inhibition of endo/exocytosis in promastigotes of Leishmania amazonensis. PLA2 activities were assayed in intact parasites, in whole conditioned media, and in soluble and extracellular vesicles (EVs) conditioned media fractions. BEL did not affect the viability of promastigotes, but reduced the differentiation into metacyclic forms. Intact parasites and EVs had BEL-sensitive iPLA2 activity. BEL treatment reduced total EVs secretion, as evidenced by reduced total protein concentration, as well as its size distribution and vesicles in the flagellar pocket of treated parasites as observed by TEM. Membrane proteins, such as acid phosphatases and GP63, became concentrated in the cytoplasm, mainly in multivesicular tubules of the endocytic pathway. BEL also prevented the endocytosis of BSA, transferrin and ConA, with the accumulation of these markers in the flagellar pocket. These results suggested that the activity inhibited by BEL, which is one of the irreversible inhibitors of iPLA2, is required for both endocytosis and exocytosis in promastigotes of L. amazonensis.
topic Leishmania amazonensis
bromoenol lactone (BEL)
endocytic pathways
exocytic pathways
ultrastructure
calcium-independent phospholipase A2
url https://www.frontiersin.org/article/10.3389/fcimb.2020.00039/full
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spelling doaj-2e482428e7c54160acc85c2b2dd09cc32020-11-25T00:26:58ZengFrontiers Media S.A.Frontiers in Cellular and Infection Microbiology2235-29882020-02-011010.3389/fcimb.2020.00039496207Endocytosis and Exocytosis in Leishmania amazonensis Are Modulated by Bromoenol LactoneAnne C. S. Fernandes0Anne C. S. Fernandes1Deivid C. Soares2Roberta F. C. Neves3Carolina M. Koeller4Norton Heise5Camila M. Adade6Susana Frases7José R. Meyer-Fernandes8José R. Meyer-Fernandes9Elvira M. Saraiva10Thaïs Souto-Padrón11Thaïs Souto-Padrón12Centro de Ciências da Saúde, Instituto de Microbiologia Paulo de Góes, Universidade Federal Do Rio de Janeiro, Rio de Janeiro, BrazilInstituto Nacional de Ciência e Tecnologia de Biologia Estrutural e Bioimagem, Universidade Federal Do Rio de Janeiro, Rio de Janeiro, BrazilCentro de Ciências da Saúde, Instituto de Microbiologia Paulo de Góes, Universidade Federal Do Rio de Janeiro, Rio de Janeiro, BrazilCentro de Ciências da Saúde, Instituto de Microbiologia Paulo de Góes, Universidade Federal Do Rio de Janeiro, Rio de Janeiro, BrazilInstituto de Biofísica Carlos Chagas Filho, Universidade Federal Do Rio de Janeiro, Rio de Janeiro, BrazilInstituto de Biofísica Carlos Chagas Filho, Universidade Federal Do Rio de Janeiro, Rio de Janeiro, BrazilCentro de Ciências da Saúde, Instituto de Microbiologia Paulo de Góes, Universidade Federal Do Rio de Janeiro, Rio de Janeiro, BrazilLaboratório de Ultraestrutura Celular Hertha Meyer, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal Do Rio de Janeiro, Rio de Janeiro, BrazilInstituto Nacional de Ciência e Tecnologia de Biologia Estrutural e Bioimagem, Universidade Federal Do Rio de Janeiro, Rio de Janeiro, BrazilCentro de Ciências da Saúde, Instituto de Bioquímica Médica Leopoldo de Meis, Universidade Federal Do Rio de Janeiro, Rio de Janeiro, BrazilCentro de Ciências da Saúde, Instituto de Microbiologia Paulo de Góes, Universidade Federal Do Rio de Janeiro, Rio de Janeiro, BrazilCentro de Ciências da Saúde, Instituto de Microbiologia Paulo de Góes, Universidade Federal Do Rio de Janeiro, Rio de Janeiro, BrazilInstituto Nacional de Ciência e Tecnologia de Biologia Estrutural e Bioimagem, Universidade Federal Do Rio de Janeiro, Rio de Janeiro, BrazilIn the protozoan pathogen Leishmania, endocytosis, and exocytosis occur mainly in the small area of the flagellar pocket membrane, which makes this parasite an interesting model of strikingly polarized internalization and secretion. Moreover, little is known about vesicle recognition and fusion mechanisms, which are essential for both endo/exocytosis in this parasite. In other cell types, vesicle fusion events require the activity of phospholipase A2 (PLA2), including Ca2+-independent iPLA2 and soluble, Ca2+-dependent sPLA2. Here, we studied the role of bromoenol lactone (BEL) inhibition of endo/exocytosis in promastigotes of Leishmania amazonensis. PLA2 activities were assayed in intact parasites, in whole conditioned media, and in soluble and extracellular vesicles (EVs) conditioned media fractions. BEL did not affect the viability of promastigotes, but reduced the differentiation into metacyclic forms. Intact parasites and EVs had BEL-sensitive iPLA2 activity. BEL treatment reduced total EVs secretion, as evidenced by reduced total protein concentration, as well as its size distribution and vesicles in the flagellar pocket of treated parasites as observed by TEM. Membrane proteins, such as acid phosphatases and GP63, became concentrated in the cytoplasm, mainly in multivesicular tubules of the endocytic pathway. BEL also prevented the endocytosis of BSA, transferrin and ConA, with the accumulation of these markers in the flagellar pocket. These results suggested that the activity inhibited by BEL, which is one of the irreversible inhibitors of iPLA2, is required for both endocytosis and exocytosis in promastigotes of L. amazonensis.https://www.frontiersin.org/article/10.3389/fcimb.2020.00039/fullLeishmania amazonensisbromoenol lactone (BEL)endocytic pathwaysexocytic pathwaysultrastructurecalcium-independent phospholipase A2