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A Novel Antimicrobial Peptide Sparamosin(26–54) From the Mud Crab Scylla paramamosain Showing Potent Antifungal Activity Against Cryptococcus neoformans
Due to the increasing prevalence of drug-resistant fungi and the limitations of current treatment strategies to fungal infections, exploration and development of new antifungal drugs or substituents are necessary. In the study, a novel antimicrobial peptide, named Sparamosin, was identified in the m...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8531530/ https://www.ncbi.nlm.nih.gov/pubmed/34690992 http://dx.doi.org/10.3389/fmicb.2021.746006 |
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author | Chen, Yan-Chao Yang, Ying Zhang, Chang Chen, Hui-Yun Chen, Fangyi Wang, Ke-Jian |
author_facet | Chen, Yan-Chao Yang, Ying Zhang, Chang Chen, Hui-Yun Chen, Fangyi Wang, Ke-Jian |
author_sort | Chen, Yan-Chao |
collection | PubMed |
description | Due to the increasing prevalence of drug-resistant fungi and the limitations of current treatment strategies to fungal infections, exploration and development of new antifungal drugs or substituents are necessary. In the study, a novel antimicrobial peptide, named Sparamosin, was identified in the mud crab Scylla paramamosain, which contains a signal peptide of 22 amino acids and a mature peptide of 54 amino acids. The antimicrobial activity of its synthetic mature peptide and two truncated peptides (Sparamosin(1–25) and Sparamosin(26–54)) were determined. The results showed that Sparamosin(26–54) had the strongest activity against a variety of Gram-negative bacteria, Gram-positive bacteria and fungi, in particular had rapid fungicidal kinetics (killed 99% Cryptococcus neoformans within 10 min) and had potent anti-biofilm activity against C. neoformans, but had no cytotoxic effect on mammalian cells. The RNA-seq results showed that after Sparamosin(26–54) treatment, the expression of genes involved in cell wall component biosynthesis, cell wall integrity signaling pathway, anti-oxidative stress, apoptosis and DNA repair were significantly up-regulated, indicating that Sparamosin(26–54) might disrupt the cell wall of C. neoformans, causing oxidative stress, DNA damage and cell apoptosis. The underlying mechanism was further confirmed. Sparamosin(26–54) could bind to several phospholipids in the cell membrane and effectively killed C. neoformans through disrupting the integrity of the cell wall and cell membrane observed by electron microscope and staining assay. In addition, it was found that the accumulation of reactive oxygen species (ROS) increased, the mitochondrial membrane potential (MMP) was disrupted, and DNA fragmentation was induced after Sparamosin(26–54) treatment, which are all hallmarks of apoptosis. Taken together, Sparamosin(26–54) has a good application prospect as an effective antimicrobial agent, especially for C. neoformans infections. |
format | Online Article Text |
id | pubmed-8531530 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85315302021-10-23 A Novel Antimicrobial Peptide Sparamosin(26–54) From the Mud Crab Scylla paramamosain Showing Potent Antifungal Activity Against Cryptococcus neoformans Chen, Yan-Chao Yang, Ying Zhang, Chang Chen, Hui-Yun Chen, Fangyi Wang, Ke-Jian Front Microbiol Microbiology Due to the increasing prevalence of drug-resistant fungi and the limitations of current treatment strategies to fungal infections, exploration and development of new antifungal drugs or substituents are necessary. In the study, a novel antimicrobial peptide, named Sparamosin, was identified in the mud crab Scylla paramamosain, which contains a signal peptide of 22 amino acids and a mature peptide of 54 amino acids. The antimicrobial activity of its synthetic mature peptide and two truncated peptides (Sparamosin(1–25) and Sparamosin(26–54)) were determined. The results showed that Sparamosin(26–54) had the strongest activity against a variety of Gram-negative bacteria, Gram-positive bacteria and fungi, in particular had rapid fungicidal kinetics (killed 99% Cryptococcus neoformans within 10 min) and had potent anti-biofilm activity against C. neoformans, but had no cytotoxic effect on mammalian cells. The RNA-seq results showed that after Sparamosin(26–54) treatment, the expression of genes involved in cell wall component biosynthesis, cell wall integrity signaling pathway, anti-oxidative stress, apoptosis and DNA repair were significantly up-regulated, indicating that Sparamosin(26–54) might disrupt the cell wall of C. neoformans, causing oxidative stress, DNA damage and cell apoptosis. The underlying mechanism was further confirmed. Sparamosin(26–54) could bind to several phospholipids in the cell membrane and effectively killed C. neoformans through disrupting the integrity of the cell wall and cell membrane observed by electron microscope and staining assay. In addition, it was found that the accumulation of reactive oxygen species (ROS) increased, the mitochondrial membrane potential (MMP) was disrupted, and DNA fragmentation was induced after Sparamosin(26–54) treatment, which are all hallmarks of apoptosis. Taken together, Sparamosin(26–54) has a good application prospect as an effective antimicrobial agent, especially for C. neoformans infections. Frontiers Media S.A. 2021-10-08 /pmc/articles/PMC8531530/ /pubmed/34690992 http://dx.doi.org/10.3389/fmicb.2021.746006 Text en Copyright © 2021 Chen, Yang, Zhang, Chen, Chen and Wang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Chen, Yan-Chao Yang, Ying Zhang, Chang Chen, Hui-Yun Chen, Fangyi Wang, Ke-Jian A Novel Antimicrobial Peptide Sparamosin(26–54) From the Mud Crab Scylla paramamosain Showing Potent Antifungal Activity Against Cryptococcus neoformans |
title | A Novel Antimicrobial Peptide Sparamosin(26–54) From the Mud Crab Scylla paramamosain Showing Potent Antifungal Activity Against Cryptococcus neoformans |
title_full | A Novel Antimicrobial Peptide Sparamosin(26–54) From the Mud Crab Scylla paramamosain Showing Potent Antifungal Activity Against Cryptococcus neoformans |
title_fullStr | A Novel Antimicrobial Peptide Sparamosin(26–54) From the Mud Crab Scylla paramamosain Showing Potent Antifungal Activity Against Cryptococcus neoformans |
title_full_unstemmed | A Novel Antimicrobial Peptide Sparamosin(26–54) From the Mud Crab Scylla paramamosain Showing Potent Antifungal Activity Against Cryptococcus neoformans |
title_short | A Novel Antimicrobial Peptide Sparamosin(26–54) From the Mud Crab Scylla paramamosain Showing Potent Antifungal Activity Against Cryptococcus neoformans |
title_sort | novel antimicrobial peptide sparamosin(26–54) from the mud crab scylla paramamosain showing potent antifungal activity against cryptococcus neoformans |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8531530/ https://www.ncbi.nlm.nih.gov/pubmed/34690992 http://dx.doi.org/10.3389/fmicb.2021.746006 |
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