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In silico characterization of cysteine-stabilized αβ defensins from neglected unicellular microeukaryotes

BACKGROUND: The emergence of multi-resistant pathogens have increased dramatically in recent years, becoming a major public-health concern. Among other promising antimicrobial molecules with potential to assist in this worldwide struggle, cysteine-stabilized αβ (CS-αβ) defensins are attracting atten...

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Autor principal: Senra, Marcus Vinicius Xavier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10040121/
https://www.ncbi.nlm.nih.gov/pubmed/36966312
http://dx.doi.org/10.1186/s12866-023-02817-w
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author Senra, Marcus Vinicius Xavier
author_facet Senra, Marcus Vinicius Xavier
author_sort Senra, Marcus Vinicius Xavier
collection PubMed
description BACKGROUND: The emergence of multi-resistant pathogens have increased dramatically in recent years, becoming a major public-health concern. Among other promising antimicrobial molecules with potential to assist in this worldwide struggle, cysteine-stabilized αβ (CS-αβ) defensins are attracting attention due their efficacy, stability, and broad spectrum against viruses, bacteria, fungi, and protists, including many known human pathogens. RESULTS: Here, 23 genomes of ciliated protists were screened and two CS-αβ defensins with a likely antifungal activity were identified and characterized, using bioinformatics, from a culturable freshwater species, Laurentiella sp. (LsAMP-1 and LsAMP-2). Although any potential cellular ligand could be predicted for LsAMP-2; evidences from structural, molecular dynamics, and docking analyses suggest that LsAMP-1 may form stably associations with phosphatidylinositol 4,5-bisphosphates (PIP2), a phospholipid found on many eukaryotic cells, which could, in turn, represent an anchorage mechanism within plasma membrane of targeted cells. CONCLUSION: These data stress that more biotechnology-oriented studies should be conducted on neglected protists, such ciliates, which could become valuable sources of novel bioactive molecules for therapeutic uses. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-023-02817-w.
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spelling pubmed-100401212023-03-27 In silico characterization of cysteine-stabilized αβ defensins from neglected unicellular microeukaryotes Senra, Marcus Vinicius Xavier BMC Microbiol Research BACKGROUND: The emergence of multi-resistant pathogens have increased dramatically in recent years, becoming a major public-health concern. Among other promising antimicrobial molecules with potential to assist in this worldwide struggle, cysteine-stabilized αβ (CS-αβ) defensins are attracting attention due their efficacy, stability, and broad spectrum against viruses, bacteria, fungi, and protists, including many known human pathogens. RESULTS: Here, 23 genomes of ciliated protists were screened and two CS-αβ defensins with a likely antifungal activity were identified and characterized, using bioinformatics, from a culturable freshwater species, Laurentiella sp. (LsAMP-1 and LsAMP-2). Although any potential cellular ligand could be predicted for LsAMP-2; evidences from structural, molecular dynamics, and docking analyses suggest that LsAMP-1 may form stably associations with phosphatidylinositol 4,5-bisphosphates (PIP2), a phospholipid found on many eukaryotic cells, which could, in turn, represent an anchorage mechanism within plasma membrane of targeted cells. CONCLUSION: These data stress that more biotechnology-oriented studies should be conducted on neglected protists, such ciliates, which could become valuable sources of novel bioactive molecules for therapeutic uses. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-023-02817-w. BioMed Central 2023-03-25 /pmc/articles/PMC10040121/ /pubmed/36966312 http://dx.doi.org/10.1186/s12866-023-02817-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Senra, Marcus Vinicius Xavier
In silico characterization of cysteine-stabilized αβ defensins from neglected unicellular microeukaryotes
title In silico characterization of cysteine-stabilized αβ defensins from neglected unicellular microeukaryotes
title_full In silico characterization of cysteine-stabilized αβ defensins from neglected unicellular microeukaryotes
title_fullStr In silico characterization of cysteine-stabilized αβ defensins from neglected unicellular microeukaryotes
title_full_unstemmed In silico characterization of cysteine-stabilized αβ defensins from neglected unicellular microeukaryotes
title_short In silico characterization of cysteine-stabilized αβ defensins from neglected unicellular microeukaryotes
title_sort in silico characterization of cysteine-stabilized αβ defensins from neglected unicellular microeukaryotes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10040121/
https://www.ncbi.nlm.nih.gov/pubmed/36966312
http://dx.doi.org/10.1186/s12866-023-02817-w
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