Intracellular zinc flux causes reactive oxygen species mediated mitochondrial dysfunction leading to cell death in Leishmania donovani.

Leishmaniasis caused by Leishmania parasite is a global threat to public health and one of the most neglected tropical diseases. Therefore, the discovery of novel drug targets and effective drug is a major challenge and an important goal. Leishmania is an obligate intracellular parasite that alterna...

Full description

Bibliographic Details
Main Authors: Anjali Kumari, Krishn Pratap Singh, Abhishek Mandal, Ranjeet Kumar Paswan, Preeti Sinha, Pradeep Das, Vahab Ali, Sanjiva Bimal, Chandra Shekhar Lal
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5460814?pdf=render
_version_ 1818233561341231104
author Anjali Kumari
Krishn Pratap Singh
Abhishek Mandal
Ranjeet Kumar Paswan
Preeti Sinha
Pradeep Das
Vahab Ali
Sanjiva Bimal
Chandra Shekhar Lal
author_facet Anjali Kumari
Krishn Pratap Singh
Abhishek Mandal
Ranjeet Kumar Paswan
Preeti Sinha
Pradeep Das
Vahab Ali
Sanjiva Bimal
Chandra Shekhar Lal
author_sort Anjali Kumari
collection DOAJ
description Leishmaniasis caused by Leishmania parasite is a global threat to public health and one of the most neglected tropical diseases. Therefore, the discovery of novel drug targets and effective drug is a major challenge and an important goal. Leishmania is an obligate intracellular parasite that alternates between sand fly and human host. To survive and establish infections, Leishmania parasites scavenge and internalize nutrients from the host. Nevertheless, host cells presents mechanism like nutrient restriction to inhibit microbial growth and control infection. Zinc is crucial for cellular growth and disruption in its homeostasis hinders growth and survival in many cells. However, little is known about the role of zinc in Leishmania growth and survival. In this study, the effect of zinc on the growth and survival of L.donovani was analyzed by both Zinc-depletion and Zinc-supplementation using Zinc-specific chelator N, N, N', N'-tetrakis (2-pyridylmethyl) ethylenediamine (TPEN) and Zinc Sulfate (ZnSO4). Treatment of parasites with TPEN rather than ZnSO4 had significantly affected the growth in a dose- and time-dependent manner. The pre-treatment of promastigotes with TPEN resulted into reduced host-parasite interaction as indicated by decreased association index. Zn depletion resulted into flux in intracellular labile Zn pool and increased in ROS generation correlated with decreased intracellular total thiol and retention of plasma membrane integrity without phosphatidylserine exposure in TPEN treated promastigotes. We also observed that TPEN-induced Zn depletion resulted into collapse of mitochondrial membrane potential which is associated with increase in cytosolic calcium and cytochrome-c. DNA fragmentation analysis showed increased DNA fragments in Zn-depleted cells. In summary, intracellular Zn depletion in the L. donovani promastigotes led to ROS-mediated caspase-independent mitochondrial dysfunction resulting into apoptosis-like cell death. Therefore, cellular zinc homeostasis in Leishmania can be explored for new drug targets and chemotherapeutics to control Leishmanial growth and disease progression.
first_indexed 2024-12-12T11:24:08Z
format Article
id doaj.art-60fb2b43ed974266bf81918e2248444a
institution Directory Open Access Journal
issn 1932-6203
language English
last_indexed 2024-12-12T11:24:08Z
publishDate 2017-01-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS ONE
spelling doaj.art-60fb2b43ed974266bf81918e2248444a2022-12-22T00:25:57ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-01126e017880010.1371/journal.pone.0178800Intracellular zinc flux causes reactive oxygen species mediated mitochondrial dysfunction leading to cell death in Leishmania donovani.Anjali KumariKrishn Pratap SinghAbhishek MandalRanjeet Kumar PaswanPreeti SinhaPradeep DasVahab AliSanjiva BimalChandra Shekhar LalLeishmaniasis caused by Leishmania parasite is a global threat to public health and one of the most neglected tropical diseases. Therefore, the discovery of novel drug targets and effective drug is a major challenge and an important goal. Leishmania is an obligate intracellular parasite that alternates between sand fly and human host. To survive and establish infections, Leishmania parasites scavenge and internalize nutrients from the host. Nevertheless, host cells presents mechanism like nutrient restriction to inhibit microbial growth and control infection. Zinc is crucial for cellular growth and disruption in its homeostasis hinders growth and survival in many cells. However, little is known about the role of zinc in Leishmania growth and survival. In this study, the effect of zinc on the growth and survival of L.donovani was analyzed by both Zinc-depletion and Zinc-supplementation using Zinc-specific chelator N, N, N', N'-tetrakis (2-pyridylmethyl) ethylenediamine (TPEN) and Zinc Sulfate (ZnSO4). Treatment of parasites with TPEN rather than ZnSO4 had significantly affected the growth in a dose- and time-dependent manner. The pre-treatment of promastigotes with TPEN resulted into reduced host-parasite interaction as indicated by decreased association index. Zn depletion resulted into flux in intracellular labile Zn pool and increased in ROS generation correlated with decreased intracellular total thiol and retention of plasma membrane integrity without phosphatidylserine exposure in TPEN treated promastigotes. We also observed that TPEN-induced Zn depletion resulted into collapse of mitochondrial membrane potential which is associated with increase in cytosolic calcium and cytochrome-c. DNA fragmentation analysis showed increased DNA fragments in Zn-depleted cells. In summary, intracellular Zn depletion in the L. donovani promastigotes led to ROS-mediated caspase-independent mitochondrial dysfunction resulting into apoptosis-like cell death. Therefore, cellular zinc homeostasis in Leishmania can be explored for new drug targets and chemotherapeutics to control Leishmanial growth and disease progression.http://europepmc.org/articles/PMC5460814?pdf=render
spellingShingle Anjali Kumari
Krishn Pratap Singh
Abhishek Mandal
Ranjeet Kumar Paswan
Preeti Sinha
Pradeep Das
Vahab Ali
Sanjiva Bimal
Chandra Shekhar Lal
Intracellular zinc flux causes reactive oxygen species mediated mitochondrial dysfunction leading to cell death in Leishmania donovani.
PLoS ONE
title Intracellular zinc flux causes reactive oxygen species mediated mitochondrial dysfunction leading to cell death in Leishmania donovani.
title_full Intracellular zinc flux causes reactive oxygen species mediated mitochondrial dysfunction leading to cell death in Leishmania donovani.
title_fullStr Intracellular zinc flux causes reactive oxygen species mediated mitochondrial dysfunction leading to cell death in Leishmania donovani.
title_full_unstemmed Intracellular zinc flux causes reactive oxygen species mediated mitochondrial dysfunction leading to cell death in Leishmania donovani.
title_short Intracellular zinc flux causes reactive oxygen species mediated mitochondrial dysfunction leading to cell death in Leishmania donovani.
title_sort intracellular zinc flux causes reactive oxygen species mediated mitochondrial dysfunction leading to cell death in leishmania donovani
url http://europepmc.org/articles/PMC5460814?pdf=render
work_keys_str_mv AT anjalikumari intracellularzincfluxcausesreactiveoxygenspeciesmediatedmitochondrialdysfunctionleadingtocelldeathinleishmaniadonovani
AT krishnpratapsingh intracellularzincfluxcausesreactiveoxygenspeciesmediatedmitochondrialdysfunctionleadingtocelldeathinleishmaniadonovani
AT abhishekmandal intracellularzincfluxcausesreactiveoxygenspeciesmediatedmitochondrialdysfunctionleadingtocelldeathinleishmaniadonovani
AT ranjeetkumarpaswan intracellularzincfluxcausesreactiveoxygenspeciesmediatedmitochondrialdysfunctionleadingtocelldeathinleishmaniadonovani
AT preetisinha intracellularzincfluxcausesreactiveoxygenspeciesmediatedmitochondrialdysfunctionleadingtocelldeathinleishmaniadonovani
AT pradeepdas intracellularzincfluxcausesreactiveoxygenspeciesmediatedmitochondrialdysfunctionleadingtocelldeathinleishmaniadonovani
AT vahabali intracellularzincfluxcausesreactiveoxygenspeciesmediatedmitochondrialdysfunctionleadingtocelldeathinleishmaniadonovani
AT sanjivabimal intracellularzincfluxcausesreactiveoxygenspeciesmediatedmitochondrialdysfunctionleadingtocelldeathinleishmaniadonovani
AT chandrashekharlal intracellularzincfluxcausesreactiveoxygenspeciesmediatedmitochondrialdysfunctionleadingtocelldeathinleishmaniadonovani