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Assays for the Identification of Novel Antivirals against Bluetongue Virus
Published on: October 11, 2013
Computational discovery of potential therapeutic agents against brain-eating amoeba (Naegleria fowleri)
Jacopo Zattoni1, Richard F Ludueña2, Maral Aminpour1
1Department of Biomedical Engineering, University of Alberta, Donadeo Innovation Centre for Engineering, Edmonton, Alberta, Canada.
Abstract:
Naegleria fowleri is a human and animal pathogen well-known for its ability to digest neurons and astrocytes of the host's brain, causing a haemorrhagic and necrotizing inflammation called Primary Amoebic Meningoencephalitis. Although infections are rare, the mortality rate is over 97%, due to both the non-specificity of the symptoms and the absence of an effective treatment. In this work we employed bioinformatics tools to evaluate the possibility of treating the infection with tubulin-targeting compounds, which we regard as the most promising approach given the unclear view on the pathogenic factors in N. fowleri, the divergence of the amoeba's tubulins from the human counterparts, and how well-established microtubule-targeting therapies are in clinical practices. The amoeba's tubulin sequences were analyzed and compared to the human tubulins to conjecture the role of their differences in drugs resistance. The binding affinity of the compounds was computed for both species by performing docking simulations using Chemical Computing Group's MOE and CCSB's AutoDock4 and AutoDock Vina. The results were analyzed using a consensus method to increase their reliability. We found that the amoeba's mitotic tubulins show a significant number of changes that are expected to decrease their affinity for tubulin-targeting compounds. We identified the Colchicine binding site as the most suitable target, and propose that Colchicine analogs retain their ability to bind to the amoeba's tubulins in vivo. The selectivity of the compounds for the pathogen however remains an issue. The changes in the amino. acid sequences in the Colchicine site could create a template for designing novel derivatives with an improved selectivity for the parasite and a safer profile for the patient. We therefore believe that our results could be the starting point for a rational derivatization of the selected ligands, leading to the development of an effective treatment for Naegleria fowleri infection.
Insights
Naegleria fowleri infections are deadly, but tubulin-targeting drugs show promise. Bioinformatics analysis identified the Colchicine binding site as a potential target for developing new treatments against this brain-eating amoeba.
Area of Science:
- Parasitology
- Computational Biology
- Drug Discovery
Background:
- Naegleria fowleri causes Primary Amoebic Meningoencephalitis, a rare but nearly fatal brain infection.
- Current treatments are ineffective due to non-specific symptoms and lack of targeted therapies.
Purpose of the Study:
- To explore the potential of tubulin-targeting compounds for treating Naegleria fowleri infections.
- To analyze differences in amoeba and human tubulins for drug resistance insights.
Main Methods:
- Bioinformatics analysis of Naegleria fowleri tubulin sequences.
- Molecular docking simulations to assess binding affinity of compounds to amoeba and human tubulins.
- Consensus analysis of docking results for reliability.
Main Results:
- Significant sequence changes in amoeba mitotic tubulins may affect drug binding.
- The Colchicine binding site was identified as a promising target.
- Colchicine analogs show potential for binding to amoeba tubulins, but selectivity remains a challenge.
Conclusions:
- Structural modifications in the Colchicine binding site offer a basis for designing more selective and safer anti-Naegleria drugs.
- This research provides a foundation for developing novel therapeutic agents against Naegleria fowleri infections.
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