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Antimicrobial activity of the toxin VdTX-I from the spider Vitalius dubius (Araneae, Theraphosidae)

BACKGROUND: Currently there is an urgent need to develop new classes of antimicrobial agents with different mechanisms of action from conventionally antibiotics used for the control of pathogenic microorganisms. The acylpolyamine called VdTX-I was isolated from the venom of the tarantula Vitalius du...

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Autores principales: Sutti, Rafael, Rosa, Bruno Bezerra, Wunderlich, Bettina, da Silva Junior, Pedro Ismael, Rocha e Silva, Thomaz Augusto Alves da
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5669311/
https://www.ncbi.nlm.nih.gov/pubmed/29124220
http://dx.doi.org/10.1016/j.bbrep.2015.09.018
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author Sutti, Rafael
Rosa, Bruno Bezerra
Wunderlich, Bettina
da Silva Junior, Pedro Ismael
Rocha e Silva, Thomaz Augusto Alves da
author_facet Sutti, Rafael
Rosa, Bruno Bezerra
Wunderlich, Bettina
da Silva Junior, Pedro Ismael
Rocha e Silva, Thomaz Augusto Alves da
author_sort Sutti, Rafael
collection PubMed
description BACKGROUND: Currently there is an urgent need to develop new classes of antimicrobial agents with different mechanisms of action from conventionally antibiotics used for the control of pathogenic microorganisms. The acylpolyamine called VdTX-I was isolated from the venom of the tarantula Vitalius dubius, and first described with activity as an antagonist of nicotinic cholinergic receptors. The main objective of this study was to investigate the antimicrobial activity found in the venom of the spider, with emphasis on the toxin VdTX-I. METHODS: Antimicrobial assays were performed in 96 well plates culture against 14 micro-organisms (fungi, yeasts and bacteria), which were tested concentrations from 0.19 to 100 μM of VdTX-I. After qualitative analysis, dose-response curve assays were performed in bacterial kill curve using MTT reagent and hemolytic assay. RESULTS: The antimicrobial activity of the VdTX-I toxin was observed in 12 tested species of Candida, Trichosporiun, Staphylococcus and Micrococcus. The toxicity had a dose-response at 3.12 µM – 100 μM in Candida albicans, Candida guillermondii, Micrococcus luteus and Escherichia coli. VdTX-I took about 5 min to inhibit bacterial growth, which was faster than streptomycin. The toxin showed no hemolytic activity between 0.19 and 100 μM. At 2.5 µg/mL of toxin it was observed no growth inhibition against a mammalian cell lineage. CONCLUSIONS: The VdTX-I toxin has a significant antimicrobial activity, with broad spectrum, and is experimentally inert to mammalian blood cells. GENERAL SIGNIFICANCE: This paper explores the antimicrobial potential of the spider toxin VdTX-I, which can provide a new model to design new antimicrobial drugs.
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spelling pubmed-56693112017-11-09 Antimicrobial activity of the toxin VdTX-I from the spider Vitalius dubius (Araneae, Theraphosidae) Sutti, Rafael Rosa, Bruno Bezerra Wunderlich, Bettina da Silva Junior, Pedro Ismael Rocha e Silva, Thomaz Augusto Alves da Biochem Biophys Rep Research Article BACKGROUND: Currently there is an urgent need to develop new classes of antimicrobial agents with different mechanisms of action from conventionally antibiotics used for the control of pathogenic microorganisms. The acylpolyamine called VdTX-I was isolated from the venom of the tarantula Vitalius dubius, and first described with activity as an antagonist of nicotinic cholinergic receptors. The main objective of this study was to investigate the antimicrobial activity found in the venom of the spider, with emphasis on the toxin VdTX-I. METHODS: Antimicrobial assays were performed in 96 well plates culture against 14 micro-organisms (fungi, yeasts and bacteria), which were tested concentrations from 0.19 to 100 μM of VdTX-I. After qualitative analysis, dose-response curve assays were performed in bacterial kill curve using MTT reagent and hemolytic assay. RESULTS: The antimicrobial activity of the VdTX-I toxin was observed in 12 tested species of Candida, Trichosporiun, Staphylococcus and Micrococcus. The toxicity had a dose-response at 3.12 µM – 100 μM in Candida albicans, Candida guillermondii, Micrococcus luteus and Escherichia coli. VdTX-I took about 5 min to inhibit bacterial growth, which was faster than streptomycin. The toxin showed no hemolytic activity between 0.19 and 100 μM. At 2.5 µg/mL of toxin it was observed no growth inhibition against a mammalian cell lineage. CONCLUSIONS: The VdTX-I toxin has a significant antimicrobial activity, with broad spectrum, and is experimentally inert to mammalian blood cells. GENERAL SIGNIFICANCE: This paper explores the antimicrobial potential of the spider toxin VdTX-I, which can provide a new model to design new antimicrobial drugs. Elsevier 2015-09-28 /pmc/articles/PMC5669311/ /pubmed/29124220 http://dx.doi.org/10.1016/j.bbrep.2015.09.018 Text en © 2015 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Sutti, Rafael
Rosa, Bruno Bezerra
Wunderlich, Bettina
da Silva Junior, Pedro Ismael
Rocha e Silva, Thomaz Augusto Alves da
Antimicrobial activity of the toxin VdTX-I from the spider Vitalius dubius (Araneae, Theraphosidae)
title Antimicrobial activity of the toxin VdTX-I from the spider Vitalius dubius (Araneae, Theraphosidae)
title_full Antimicrobial activity of the toxin VdTX-I from the spider Vitalius dubius (Araneae, Theraphosidae)
title_fullStr Antimicrobial activity of the toxin VdTX-I from the spider Vitalius dubius (Araneae, Theraphosidae)
title_full_unstemmed Antimicrobial activity of the toxin VdTX-I from the spider Vitalius dubius (Araneae, Theraphosidae)
title_short Antimicrobial activity of the toxin VdTX-I from the spider Vitalius dubius (Araneae, Theraphosidae)
title_sort antimicrobial activity of the toxin vdtx-i from the spider vitalius dubius (araneae, theraphosidae)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5669311/
https://www.ncbi.nlm.nih.gov/pubmed/29124220
http://dx.doi.org/10.1016/j.bbrep.2015.09.018
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