Targeting PrfA from Listeria monocytogenes: A computational drug repurposing approach

Humans can develop listeriosis by ingestion of foods contaminated with Listeria monocytogenes (L. monocytogenes), an opportunistic gram-positive ubiquitous bacterium. Whilst the non-invasive form of listeriosis may be asymptomatic or cause mild flu-like symptoms, the invasive form of listeriosis is...

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Main Author: Xabier Arias-Moreno
Format: Article
Language:English
Published: Elsevier 2024-12-01
Series:The Microbe
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Online Access:http://www.sciencedirect.com/science/article/pii/S2950194624001675
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author Xabier Arias-Moreno
author_facet Xabier Arias-Moreno
author_sort Xabier Arias-Moreno
collection DOAJ
description Humans can develop listeriosis by ingestion of foods contaminated with Listeria monocytogenes (L. monocytogenes), an opportunistic gram-positive ubiquitous bacterium. Whilst the non-invasive form of listeriosis may be asymptomatic or cause mild flu-like symptoms, the invasive form of listeriosis is life-threatening and is associated with high hospitalization and fatality rates. Current antibiotic-based therapies are still effective against listeriosis. However, multi-drug resistant L. monocytogenes strains have already been identified, which represents a new risk in the treatment of invasive listeriosis. Therefore, it is increasingly urgent to identify new compounds that do not target the conventional biochemical pathways disrupted by current antibiotics. Positive Regulatory Factor A (PrfA) is a well-studied transcription factor in L. monocytogenes that is responsible for activating a plethora of virulence factors. Targeting virulence factors is a promising strategy that is being considered to combat bacterial infections, hence targeting PrfA is both logical and attractive. In the present computational drug repurposing approach, a complete FDA-approved drugs dataset of more than 700 compounds was virtually screened by docking the drugs against the structure of PrfA. Three of the most promising top-scored FDA drug candidates were then simulated complexed to PrfA. Data from Molecular docking and Molecular Dynamics simulations suggest that Dutasteride binds PrfA, and as a result, may exhibit inhibitory activity against L. monocytogenes. The use of Dutasteride is safe in humans since it has been administered in the treatment of benign prostatic hyperplasia for decades. Its unique chemical scaffold may represent a valuable starting point for the rapid development of disruptive novel listeria-specific drugs that will be soon needed to combat multi-drug resistant L. monocytogenes strains.
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spelling doaj-art-989f756fb2e44e1f9f0ba72b778de6ef2025-08-20T02:37:09ZengElsevierThe Microbe2950-19462024-12-01510020010.1016/j.microb.2024.100200Targeting PrfA from Listeria monocytogenes: A computational drug repurposing approachXabier Arias-Moreno0Institute of Biomedical and Pharmaceutical Sciences, Guangdong University of Technology, Guangzhou, 510006, ChinaHumans can develop listeriosis by ingestion of foods contaminated with Listeria monocytogenes (L. monocytogenes), an opportunistic gram-positive ubiquitous bacterium. Whilst the non-invasive form of listeriosis may be asymptomatic or cause mild flu-like symptoms, the invasive form of listeriosis is life-threatening and is associated with high hospitalization and fatality rates. Current antibiotic-based therapies are still effective against listeriosis. However, multi-drug resistant L. monocytogenes strains have already been identified, which represents a new risk in the treatment of invasive listeriosis. Therefore, it is increasingly urgent to identify new compounds that do not target the conventional biochemical pathways disrupted by current antibiotics. Positive Regulatory Factor A (PrfA) is a well-studied transcription factor in L. monocytogenes that is responsible for activating a plethora of virulence factors. Targeting virulence factors is a promising strategy that is being considered to combat bacterial infections, hence targeting PrfA is both logical and attractive. In the present computational drug repurposing approach, a complete FDA-approved drugs dataset of more than 700 compounds was virtually screened by docking the drugs against the structure of PrfA. Three of the most promising top-scored FDA drug candidates were then simulated complexed to PrfA. Data from Molecular docking and Molecular Dynamics simulations suggest that Dutasteride binds PrfA, and as a result, may exhibit inhibitory activity against L. monocytogenes. The use of Dutasteride is safe in humans since it has been administered in the treatment of benign prostatic hyperplasia for decades. Its unique chemical scaffold may represent a valuable starting point for the rapid development of disruptive novel listeria-specific drugs that will be soon needed to combat multi-drug resistant L. monocytogenes strains.http://www.sciencedirect.com/science/article/pii/S2950194624001675Listeria monocytogenesListeriosisAntibiotic resistanceDrug repurposingStructure-based virtual screeningInhibitors
spellingShingle Xabier Arias-Moreno
Targeting PrfA from Listeria monocytogenes: A computational drug repurposing approach
The Microbe
Listeria monocytogenes
Listeriosis
Antibiotic resistance
Drug repurposing
Structure-based virtual screening
Inhibitors
title Targeting PrfA from Listeria monocytogenes: A computational drug repurposing approach
title_full Targeting PrfA from Listeria monocytogenes: A computational drug repurposing approach
title_fullStr Targeting PrfA from Listeria monocytogenes: A computational drug repurposing approach
title_full_unstemmed Targeting PrfA from Listeria monocytogenes: A computational drug repurposing approach
title_short Targeting PrfA from Listeria monocytogenes: A computational drug repurposing approach
title_sort targeting prfa from listeria monocytogenes a computational drug repurposing approach
topic Listeria monocytogenes
Listeriosis
Antibiotic resistance
Drug repurposing
Structure-based virtual screening
Inhibitors
url http://www.sciencedirect.com/science/article/pii/S2950194624001675
work_keys_str_mv AT xabierariasmoreno targetingprfafromlisteriamonocytogenesacomputationaldrugrepurposingapproach