Epidrugs: alternative chemotherapy targeting Theileria annulata schizont stage parasites

ABSTRACTThe growing emergence of resistance to current anti-theilerial agents necessitates the exploration of alternative approaches to drug discovery. This study evaluated the antiparasitic efficacy of 148 compounds derived from an epigenetic inhibitor library against the schizont stage of a Theile...

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Main Authors: Sonam Kamble, Sakshi Singh, Akash Suresh, Siva Singothu, Debabrata Dandesena, Vasundhra Bhandari, Paresh Sharma
Format: Article
Language:English
Published: American Society for Microbiology 2024-04-01
Series:Microbiology Spectrum
Subjects:
Online Access:https://journals.asm.org/doi/10.1128/spectrum.03258-23
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author Sonam Kamble
Sakshi Singh
Akash Suresh
Siva Singothu
Debabrata Dandesena
Vasundhra Bhandari
Paresh Sharma
author_facet Sonam Kamble
Sakshi Singh
Akash Suresh
Siva Singothu
Debabrata Dandesena
Vasundhra Bhandari
Paresh Sharma
author_sort Sonam Kamble
collection DOAJ
description ABSTRACTThe growing emergence of resistance to current anti-theilerial agents necessitates the exploration of alternative approaches to drug discovery. This study evaluated the antiparasitic efficacy of 148 compounds derived from an epigenetic inhibitor library against the schizont stage of a Theileria annulata-infected cell line. Initial screening at a concentration of 10 µM identified 27 compounds exhibiting promising anti-theilerial activity. Further investigation, including determination of the 50% inhibitory concentration (IC50) and host cell cytotoxicity assay, highlighted seven highly effective compounds (SAHA, BVT-948, Trichostatin A, Methylstat, Plumbagin, Ryuvidine, and TCE-5003) against T. annulata-infected cells. Analysis of the active compounds revealed their inhibitory action against various human targets, such as HDAC (SAHA and Trichostatin A), SET domain (Ryuvidine), PRMT (BVT-948 and TCE-5003), histone demethylase (Methylstat), and ROS/apoptosis inducer (Plumbagin). We identified gene orthologs of these targets in Theileria and conducted molecular docking studies, demonstrating effective binding of the compounds with their respective targets in the parasite, supported by in vitro data. Additionally, we performed in silico ADME/T predictions, which indicated potential mutagenic and hepatotoxic effects of Plumbagin, Methylstat, and TCE-5003, rendering them unsuitable for drug development. Conversely, SAHA, Trichostatin A, and BVT-948 showed promising characteristics and may represent potential candidates for future development as chemotherapeutic agents against tropical theileriosis. These findings provide valuable insights into the search for novel anti-theilerial drugs and offer a basis for further research in this area.IMPORTANCETheileria annulata is a protozoan parasite responsible for tropical theileriosis, a devastating disease affecting cattle. Traditional chemotherapy has limitations, and the study explores the potential of epidrugs as an alternative treatment approach. Epidrugs are compounds that modify gene expression without altering the underlying DNA sequence, offering a novel way to combat parasitic infections. This research is pivotal as it addresses the urgent need for innovative therapies against T. annulata, contributing to the development of more effective and targeted treatments for infected livestock. Successful implementation of epidrugs could not only enhance the well-being of cattle but also have broader implications for the control of parasitic diseases, showcasing the paper’s significance in advancing veterinary science and improving livestock health globally.
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spelling doaj.art-425b222d20ef4db691784a0fda9f0be22024-04-02T14:16:18ZengAmerican Society for MicrobiologyMicrobiology Spectrum2165-04972024-04-0112410.1128/spectrum.03258-23Epidrugs: alternative chemotherapy targeting Theileria annulata schizont stage parasitesSonam Kamble0Sakshi Singh1Akash Suresh2Siva Singothu3Debabrata Dandesena4Vasundhra Bhandari5Paresh Sharma6National Institute of Animal Biotechnology, Hyderabad, IndiaNational Institute of Animal Biotechnology, Hyderabad, IndiaNational Institute of Animal Biotechnology, Hyderabad, IndiaNational Institute of Pharmaceutical Education and Research, Hyderabad, IndiaNational Institute of Animal Biotechnology, Hyderabad, IndiaNational Institute of Animal Biotechnology, Hyderabad, IndiaNational Institute of Animal Biotechnology, Hyderabad, IndiaABSTRACTThe growing emergence of resistance to current anti-theilerial agents necessitates the exploration of alternative approaches to drug discovery. This study evaluated the antiparasitic efficacy of 148 compounds derived from an epigenetic inhibitor library against the schizont stage of a Theileria annulata-infected cell line. Initial screening at a concentration of 10 µM identified 27 compounds exhibiting promising anti-theilerial activity. Further investigation, including determination of the 50% inhibitory concentration (IC50) and host cell cytotoxicity assay, highlighted seven highly effective compounds (SAHA, BVT-948, Trichostatin A, Methylstat, Plumbagin, Ryuvidine, and TCE-5003) against T. annulata-infected cells. Analysis of the active compounds revealed their inhibitory action against various human targets, such as HDAC (SAHA and Trichostatin A), SET domain (Ryuvidine), PRMT (BVT-948 and TCE-5003), histone demethylase (Methylstat), and ROS/apoptosis inducer (Plumbagin). We identified gene orthologs of these targets in Theileria and conducted molecular docking studies, demonstrating effective binding of the compounds with their respective targets in the parasite, supported by in vitro data. Additionally, we performed in silico ADME/T predictions, which indicated potential mutagenic and hepatotoxic effects of Plumbagin, Methylstat, and TCE-5003, rendering them unsuitable for drug development. Conversely, SAHA, Trichostatin A, and BVT-948 showed promising characteristics and may represent potential candidates for future development as chemotherapeutic agents against tropical theileriosis. These findings provide valuable insights into the search for novel anti-theilerial drugs and offer a basis for further research in this area.IMPORTANCETheileria annulata is a protozoan parasite responsible for tropical theileriosis, a devastating disease affecting cattle. Traditional chemotherapy has limitations, and the study explores the potential of epidrugs as an alternative treatment approach. Epidrugs are compounds that modify gene expression without altering the underlying DNA sequence, offering a novel way to combat parasitic infections. This research is pivotal as it addresses the urgent need for innovative therapies against T. annulata, contributing to the development of more effective and targeted treatments for infected livestock. Successful implementation of epidrugs could not only enhance the well-being of cattle but also have broader implications for the control of parasitic diseases, showcasing the paper’s significance in advancing veterinary science and improving livestock health globally.https://journals.asm.org/doi/10.1128/spectrum.03258-23epigenetic inhibitorsTheileriadrug repurposingapoptosisapicomplexan
spellingShingle Sonam Kamble
Sakshi Singh
Akash Suresh
Siva Singothu
Debabrata Dandesena
Vasundhra Bhandari
Paresh Sharma
Epidrugs: alternative chemotherapy targeting Theileria annulata schizont stage parasites
Microbiology Spectrum
epigenetic inhibitors
Theileria
drug repurposing
apoptosis
apicomplexan
title Epidrugs: alternative chemotherapy targeting Theileria annulata schizont stage parasites
title_full Epidrugs: alternative chemotherapy targeting Theileria annulata schizont stage parasites
title_fullStr Epidrugs: alternative chemotherapy targeting Theileria annulata schizont stage parasites
title_full_unstemmed Epidrugs: alternative chemotherapy targeting Theileria annulata schizont stage parasites
title_short Epidrugs: alternative chemotherapy targeting Theileria annulata schizont stage parasites
title_sort epidrugs alternative chemotherapy targeting theileria annulata schizont stage parasites
topic epigenetic inhibitors
Theileria
drug repurposing
apoptosis
apicomplexan
url https://journals.asm.org/doi/10.1128/spectrum.03258-23
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AT sivasingothu epidrugsalternativechemotherapytargetingtheileriaannulataschizontstageparasites
AT debabratadandesena epidrugsalternativechemotherapytargetingtheileriaannulataschizontstageparasites
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