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A truncated peptide Spgillcin(177–189) derived from mud crab Scylla paramamosain exerting multiple antibacterial activities
Antimicrobial peptides (AMPs) may be the most promising substitute for antibiotics due to their effective bactericidal activity and multiple antimicrobial modes against pathogenic bacteria. In this study, a new functional gene named Spgillcin was identified in Scylla paramamosain, which encoded 216...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9435603/ https://www.ncbi.nlm.nih.gov/pubmed/36061863 http://dx.doi.org/10.3389/fcimb.2022.928220 |
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author | Wang, Xiaofei Hong, Xiao Chen, Fangyi Wang, Ke-Jian |
author_facet | Wang, Xiaofei Hong, Xiao Chen, Fangyi Wang, Ke-Jian |
author_sort | Wang, Xiaofei |
collection | PubMed |
description | Antimicrobial peptides (AMPs) may be the most promising substitute for antibiotics due to their effective bactericidal activity and multiple antimicrobial modes against pathogenic bacteria. In this study, a new functional gene named Spgillcin was identified in Scylla paramamosain, which encoded 216 amino acids of mature peptide. In vivo, Spgillcin was dominantly expressed in the gills of male and female crabs, offering the highest expression level among all tested organs or tissues. The expression pattern of Spgillcin was significantly altered when challenged by Staphylococcus aureus, indicating a positive immune response. In vitro, a functional truncated peptide Spgillcin(177–189) derived from the amino acid sequence of Spgillcin was synthesized and showed a broad-spectrum and potent antibacterial activity against several bacterial strains, including the clinical isolates of multidrug-resistant (MDR) strains, with a range of minimum inhibitory concentrations from 1.5 to 48 μM. Spgillcin(177–189) also showed rapid bactericidal kinetics for S. aureus and Pseudomonas aeruginosa but did not display any cytotoxicity to mammalian cells and maintained its antimicrobial activity in different conditions. Mechanistic studies indicated that Spgillcin(177–189) was mainly involved in the disruption of cell membrane integrity where the membrane components lipoteichoic acid and lipopolysaccharide could significantly inhibit the antimicrobial activity in a dose-dependent manner. In addition, Spgillcin(177–189) could change the membrane permeability and cause the accumulation of intracellular reactive oxygen species. No resistance was generated to Spgillcin(177–189) when the clinical isolates of methicillin-resistant S. aureus and MDR P. aeruginosa were treated with Spgillcin(177–189) and then subjected to a long term of continuous culturing for 50 days. In addition, Spgillcin(177–189) exerted a strong anti-biofilm activity by inhibiting biofilm formation and was also effective at killing extracellular S. aureus in the cultural supernatant of RAW 264.7 cells. Taken together, Spgillcin(177–189) has strong potential as a substitute for antibiotics in future aquaculture and medical applications. |
format | Online Article Text |
id | pubmed-9435603 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94356032022-09-02 A truncated peptide Spgillcin(177–189) derived from mud crab Scylla paramamosain exerting multiple antibacterial activities Wang, Xiaofei Hong, Xiao Chen, Fangyi Wang, Ke-Jian Front Cell Infect Microbiol Cellular and Infection Microbiology Antimicrobial peptides (AMPs) may be the most promising substitute for antibiotics due to their effective bactericidal activity and multiple antimicrobial modes against pathogenic bacteria. In this study, a new functional gene named Spgillcin was identified in Scylla paramamosain, which encoded 216 amino acids of mature peptide. In vivo, Spgillcin was dominantly expressed in the gills of male and female crabs, offering the highest expression level among all tested organs or tissues. The expression pattern of Spgillcin was significantly altered when challenged by Staphylococcus aureus, indicating a positive immune response. In vitro, a functional truncated peptide Spgillcin(177–189) derived from the amino acid sequence of Spgillcin was synthesized and showed a broad-spectrum and potent antibacterial activity against several bacterial strains, including the clinical isolates of multidrug-resistant (MDR) strains, with a range of minimum inhibitory concentrations from 1.5 to 48 μM. Spgillcin(177–189) also showed rapid bactericidal kinetics for S. aureus and Pseudomonas aeruginosa but did not display any cytotoxicity to mammalian cells and maintained its antimicrobial activity in different conditions. Mechanistic studies indicated that Spgillcin(177–189) was mainly involved in the disruption of cell membrane integrity where the membrane components lipoteichoic acid and lipopolysaccharide could significantly inhibit the antimicrobial activity in a dose-dependent manner. In addition, Spgillcin(177–189) could change the membrane permeability and cause the accumulation of intracellular reactive oxygen species. No resistance was generated to Spgillcin(177–189) when the clinical isolates of methicillin-resistant S. aureus and MDR P. aeruginosa were treated with Spgillcin(177–189) and then subjected to a long term of continuous culturing for 50 days. In addition, Spgillcin(177–189) exerted a strong anti-biofilm activity by inhibiting biofilm formation and was also effective at killing extracellular S. aureus in the cultural supernatant of RAW 264.7 cells. Taken together, Spgillcin(177–189) has strong potential as a substitute for antibiotics in future aquaculture and medical applications. Frontiers Media S.A. 2022-08-02 /pmc/articles/PMC9435603/ /pubmed/36061863 http://dx.doi.org/10.3389/fcimb.2022.928220 Text en Copyright © 2022 Wang, Hong, 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 | Cellular and Infection Microbiology Wang, Xiaofei Hong, Xiao Chen, Fangyi Wang, Ke-Jian A truncated peptide Spgillcin(177–189) derived from mud crab Scylla paramamosain exerting multiple antibacterial activities |
title | A truncated peptide Spgillcin(177–189) derived from mud crab Scylla paramamosain exerting multiple antibacterial activities |
title_full | A truncated peptide Spgillcin(177–189) derived from mud crab Scylla paramamosain exerting multiple antibacterial activities |
title_fullStr | A truncated peptide Spgillcin(177–189) derived from mud crab Scylla paramamosain exerting multiple antibacterial activities |
title_full_unstemmed | A truncated peptide Spgillcin(177–189) derived from mud crab Scylla paramamosain exerting multiple antibacterial activities |
title_short | A truncated peptide Spgillcin(177–189) derived from mud crab Scylla paramamosain exerting multiple antibacterial activities |
title_sort | truncated peptide spgillcin(177–189) derived from mud crab scylla paramamosain exerting multiple antibacterial activities |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9435603/ https://www.ncbi.nlm.nih.gov/pubmed/36061863 http://dx.doi.org/10.3389/fcimb.2022.928220 |
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