Characterization of Monoamine Oxidase-A in tropical liver fluke, Fasciola gigantica

Fasciola gigantica, responsible for the zoonotic disease fasciolosis, pose a great threat to the livestock and human health worldwide. The triclabendazole (TCBZ) has been used for decades as a broad spectrum anthelmintic to control this perilous disease but the emergence of resistance in flukes agai...

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Main Authors: Mirza Ahmar Beg, Abdur Rehman, Lubna Rehman, Rizwan Ullah, Faiza Farhat, Sobia Wasim, S. M. A. Abidi
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2023-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10138849/?tool=EBI
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author Mirza Ahmar Beg
Abdur Rehman
Lubna Rehman
Rizwan Ullah
Faiza Farhat
Sobia Wasim
S. M. A. Abidi
author_facet Mirza Ahmar Beg
Abdur Rehman
Lubna Rehman
Rizwan Ullah
Faiza Farhat
Sobia Wasim
S. M. A. Abidi
author_sort Mirza Ahmar Beg
collection DOAJ
description Fasciola gigantica, responsible for the zoonotic disease fasciolosis, pose a great threat to the livestock and human health worldwide. The triclabendazole (TCBZ) has been used for decades as a broad spectrum anthelmintic to control this perilous disease but the emergence of resistance in flukes against TCBZ has prompted researchers across the world to explore for new drugs and antigenic targets. World Health Organization has strongly recommended the utilization of neurobiologically significant biomolecules as new drug/antigenic targets because of their significant role in the physiology of parasites. Monoamine Oxidase (MAO) is an important neurobiological enzyme which catabolizes aminergic neurotransmitters thus preventing prolonged excitation of neurons and in non-neuronal cells it prevents cellular toxicity due to accumulation of toxic monoamines. Owing to the important role of MAO in the survival and perpetuation of parasites, multipronged approaches were undertaken for the characterization of MAO-A in F. gigantica. The activity of MAO was found to be 1.5 times higher in the mitochondrial samples than the whole homogenate samples. The adult worms of the F. gigantica appeared to possess both the isoforms of MAO i.e., MAO-A and MAO-B. The zymographic studies revealed strong enzyme activity in its native state as assessed through prominent dark bands at 250KDa in the zymogram. The enzyme was also found to be highly immunogenic as revealed by high antibody titer at 1:6400 dilution. The immunogenicity of MAO-A enzyme was further established in the Western Blots in which a strong band of 50KDa was distinctly evident. Despite ubiquitous presence of MAO in F. gigantica some regions like tegumental surface and intestinal caecae displayed strong immunofluorescence as compared to other regions. The detection of MAO-A in the F. gigantica samples in Dot-Blot assay indicate a great potential of this molecule for the immunodiagnostics of fasciolosis, particularly in the field conditions. The enzyme activity was sensitive to the specific inhibitor clorgyline in a concentration dependant manner, particularly in the late incubation period. The zymographic results also exhibited similar trend. The strong intensity of spots in Dot-blots indicate high immunogenicity of the MAO protein. The intensity of bands/spots in the samples of worms treated with clorgyline also declined, clearly indicating that the tropical liver fluke possesses prominent MAO-A activity.
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spelling doaj.art-412ee9e6aa934463b299d0eb12430ed62023-05-01T05:31:24ZengPublic Library of Science (PLoS)PLoS ONE1932-62032023-01-01184Characterization of Monoamine Oxidase-A in tropical liver fluke, Fasciola giganticaMirza Ahmar BegAbdur RehmanLubna RehmanRizwan UllahFaiza FarhatSobia WasimS. M. A. AbidiFasciola gigantica, responsible for the zoonotic disease fasciolosis, pose a great threat to the livestock and human health worldwide. The triclabendazole (TCBZ) has been used for decades as a broad spectrum anthelmintic to control this perilous disease but the emergence of resistance in flukes against TCBZ has prompted researchers across the world to explore for new drugs and antigenic targets. World Health Organization has strongly recommended the utilization of neurobiologically significant biomolecules as new drug/antigenic targets because of their significant role in the physiology of parasites. Monoamine Oxidase (MAO) is an important neurobiological enzyme which catabolizes aminergic neurotransmitters thus preventing prolonged excitation of neurons and in non-neuronal cells it prevents cellular toxicity due to accumulation of toxic monoamines. Owing to the important role of MAO in the survival and perpetuation of parasites, multipronged approaches were undertaken for the characterization of MAO-A in F. gigantica. The activity of MAO was found to be 1.5 times higher in the mitochondrial samples than the whole homogenate samples. The adult worms of the F. gigantica appeared to possess both the isoforms of MAO i.e., MAO-A and MAO-B. The zymographic studies revealed strong enzyme activity in its native state as assessed through prominent dark bands at 250KDa in the zymogram. The enzyme was also found to be highly immunogenic as revealed by high antibody titer at 1:6400 dilution. The immunogenicity of MAO-A enzyme was further established in the Western Blots in which a strong band of 50KDa was distinctly evident. Despite ubiquitous presence of MAO in F. gigantica some regions like tegumental surface and intestinal caecae displayed strong immunofluorescence as compared to other regions. The detection of MAO-A in the F. gigantica samples in Dot-Blot assay indicate a great potential of this molecule for the immunodiagnostics of fasciolosis, particularly in the field conditions. The enzyme activity was sensitive to the specific inhibitor clorgyline in a concentration dependant manner, particularly in the late incubation period. The zymographic results also exhibited similar trend. The strong intensity of spots in Dot-blots indicate high immunogenicity of the MAO protein. The intensity of bands/spots in the samples of worms treated with clorgyline also declined, clearly indicating that the tropical liver fluke possesses prominent MAO-A activity.https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10138849/?tool=EBI
spellingShingle Mirza Ahmar Beg
Abdur Rehman
Lubna Rehman
Rizwan Ullah
Faiza Farhat
Sobia Wasim
S. M. A. Abidi
Characterization of Monoamine Oxidase-A in tropical liver fluke, Fasciola gigantica
PLoS ONE
title Characterization of Monoamine Oxidase-A in tropical liver fluke, Fasciola gigantica
title_full Characterization of Monoamine Oxidase-A in tropical liver fluke, Fasciola gigantica
title_fullStr Characterization of Monoamine Oxidase-A in tropical liver fluke, Fasciola gigantica
title_full_unstemmed Characterization of Monoamine Oxidase-A in tropical liver fluke, Fasciola gigantica
title_short Characterization of Monoamine Oxidase-A in tropical liver fluke, Fasciola gigantica
title_sort characterization of monoamine oxidase a in tropical liver fluke fasciola gigantica
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10138849/?tool=EBI
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