skip to main content
OSTI.GOV title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: Loss of virulence in NAD(P)H cytochrome b5 oxidoreductase deficient Leishmania major

Journal Article · · Biochemical and Biophysical Research Communications
; ; ; ; ;  [1]
  1. From the Division of Structural Biology & Bio-informatics, CSIR-Indian Institute of Chemical Biology, 4, Raja S.C. Mullick Road, Kolkata, 700 032 (India)

Highlights: • Linoleate is an absolute requirement for Leishmania promastigote survival. • Linoleate deficient Leishmania shows avirulence. • Parasite derived linoleate inactivates NF-κB signaling pathway. • Leishmanial linoleate inhibits both COX-2 and TNF-α expression in macrophage. • Supplementing external linoleate reverts most of the observed phenotypes. Leishmania promastigotes have the ability to synthesize essential polyunsaturated fatty acids de novo and can grow in lipid free media. Recently, we have shown that NAD(P)H cytochrome b5 oxidoreductase (Ncb5or) enzyme in Leishmania acts as the redox partner for Δ12 fatty acid desaturase, which catalyses the conversion of oleate to linoleate. So far, the exact role of Leishmania derived linoleate synthesis is still incomplete in the literature. The viability assay by flow cytometry as well as microscopic studies suggests that linoleate is an absolute requirement for Leishmania promastigote survival in delipidated media. Western blot analysis suggested that infection with log phase linoleate deficient mutant (KO) results in increased level of NF-κBp65, IκB and IKKβ phosphorylation in RAW264.7 cells. Similarly, the log phase KO infected RAW264.7 cells show dramatic increment of COX-2 expression and TNF-α secretion, compared to control or Ncb5or complement (CM) cell lines. The activation of inflammatory signaling pathways by KO mutant is significantly reduced when the RAW264.7 cells are pre-treated with BSA bound linoleate. Together, these findings confirmed that the leishmanial linoleate inhibits both COX-2 and TNF-α expression in macrophage via the inactivation of NF-κB signaling pathway. The stationary phase of KO promastigotes shows avirulence after infection in macrophages as well as inoculation into BALB/c mice; whereas CM cell lines show virulence. Collectively, these data provide strong evidence that de novo linoleate synthesis in Leishmania is an essential for parasite survival at extracellular promastigote stage as well as intracellular amastigote stage.

OSTI ID:
23136940
Journal Information:
Biochemical and Biophysical Research Communications, Vol. 503, Issue 1; Other Information: Copyright (c) 2018 Elsevier Inc. All rights reserved.; Country of input: International Atomic Energy Agency (IAEA); ISSN 0006-291X
Country of Publication:
United States
Language:
English

Similar Records

iRhom2 promotes atherosclerosis through macrophage inflammation and induction of oxidative stress
Journal Article · Sat Sep 15 00:00:00 EDT 2018 · Biochemical and Biophysical Research Communications · OSTI ID:23136940

Exploring the anti-inflammatory activity of a novel 2-phenylquinazoline analog with protection against inflammatory injury
Journal Article · Mon Oct 15 00:00:00 EDT 2012 · Toxicology and Applied Pharmacology · OSTI ID:23136940

Activation of AMPA receptor promotes TNF-α release via the ROS-cSrc-NFκB signaling cascade in RAW264.7 macrophages
Journal Article · Fri May 29 00:00:00 EDT 2015 · Biochemical and Biophysical Research Communications · OSTI ID:23136940