Anticandidal Activity and Mechanism of Action of Several Cationic Chimeric Antimicrobial Peptides
Antimicrobial peptides (AMPs) have recently been the subject of extensive research in both academia and commercial sectors because of their rapid, broad-spectrum microbicidal activity and a low likelihood of establishing drug resistance. Herein, we attempt to shed some light on anticandidal activity...
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Published in | International journal of peptide research and therapeutics Vol. 29; no. 3; p. 50 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Dordrecht
Springer Netherlands
06.05.2023
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Abstract | Antimicrobial peptides (AMPs) have recently been the subject of extensive research in both academia and commercial sectors because of their rapid, broad-spectrum microbicidal activity and a low likelihood of establishing drug resistance. Herein, we attempt to shed some light on anticandidal activity and mechanism of action of previously designed cationic chimeric AMPs, namely PV, BVP, PVP, and PV3. These four AMPs had a high tendency to adopt alpha-helical conformation based upon peptide structure prediction and circular dichroism. The geometric mean minimum inhibitory concentration (GMMIC) values (and ranges) of PV, BVP, PVP, and PV3 for all
Candida albicans
isolates (in µg/mL) were 1.83 (1–2), 93.33 (16 to >128), 3.25 (0.5–8), and 1.42 (0.5–2), respectively. At ≥ 8 µg/mL, all of the AMPs dose-dependently reduced in vitro viability of human fibroblast cells, with PV being the most cytotoxic peptide. Among the tested peptides, PV3 exhibited the highest cell selectivity index (determined as the ratio of CC
50
to GMMIC). Rapid candidacidal kinetics, disruption of cell wall/membrane integrity, and inhibition of yeast-to-hypha morphological switch were other important properties of the tested AMPs. Atomic force microscopy revealed that PV3 was able to induce major morpho-structural deformities in yeast cells such as blebs, cell shrinkage, and holes. Based on Fourier transform infrared-attenuated total reflectance (FTIR-ATR) spectroscopy analysis, the polysaccharide content of the yeast cells was increased markedly in response to sub-lethal doses of PV3. Despite these encouraging data, much remains to be learned about in vivo efficacy and safety of these AMPs. |
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AbstractList | Antimicrobial peptides (AMPs) have recently been the subject of extensive research in both academia and commercial sectors because of their rapid, broad-spectrum microbicidal activity and a low likelihood of establishing drug resistance. Herein, we attempt to shed some light on anticandidal activity and mechanism of action of previously designed cationic chimeric AMPs, namely PV, BVP, PVP, and PV3. These four AMPs had a high tendency to adopt alpha-helical conformation based upon peptide structure prediction and circular dichroism. The geometric mean minimum inhibitory concentration (GMMIC) values (and ranges) of PV, BVP, PVP, and PV3 for all Candida albicans isolates (in µg/mL) were 1.83 (1–2), 93.33 (16 to >128), 3.25 (0.5–8), and 1.42 (0.5–2), respectively. At ≥ 8 µg/mL, all of the AMPs dose-dependently reduced in vitro viability of human fibroblast cells, with PV being the most cytotoxic peptide. Among the tested peptides, PV3 exhibited the highest cell selectivity index (determined as the ratio of CC50 to GMMIC). Rapid candidacidal kinetics, disruption of cell wall/membrane integrity, and inhibition of yeast-to-hypha morphological switch were other important properties of the tested AMPs. Atomic force microscopy revealed that PV3 was able to induce major morpho-structural deformities in yeast cells such as blebs, cell shrinkage, and holes. Based on Fourier transform infrared-attenuated total reflectance (FTIR-ATR) spectroscopy analysis, the polysaccharide content of the yeast cells was increased markedly in response to sub-lethal doses of PV3. Despite these encouraging data, much remains to be learned about in vivo efficacy and safety of these AMPs. Antimicrobial peptides (AMPs) have recently been the subject of extensive research in both academia and commercial sectors because of their rapid, broad-spectrum microbicidal activity and a low likelihood of establishing drug resistance. Herein, we attempt to shed some light on anticandidal activity and mechanism of action of previously designed cationic chimeric AMPs, namely PV, BVP, PVP, and PV3. These four AMPs had a high tendency to adopt alpha-helical conformation based upon peptide structure prediction and circular dichroism. The geometric mean minimum inhibitory concentration (GMMIC) values (and ranges) of PV, BVP, PVP, and PV3 for all Candida albicans isolates (in µg/mL) were 1.83 (1–2), 93.33 (16 to >128), 3.25 (0.5–8), and 1.42 (0.5–2), respectively. At ≥ 8 µg/mL, all of the AMPs dose-dependently reduced in vitro viability of human fibroblast cells, with PV being the most cytotoxic peptide. Among the tested peptides, PV3 exhibited the highest cell selectivity index (determined as the ratio of CC 50 to GMMIC). Rapid candidacidal kinetics, disruption of cell wall/membrane integrity, and inhibition of yeast-to-hypha morphological switch were other important properties of the tested AMPs. Atomic force microscopy revealed that PV3 was able to induce major morpho-structural deformities in yeast cells such as blebs, cell shrinkage, and holes. Based on Fourier transform infrared-attenuated total reflectance (FTIR-ATR) spectroscopy analysis, the polysaccharide content of the yeast cells was increased markedly in response to sub-lethal doses of PV3. Despite these encouraging data, much remains to be learned about in vivo efficacy and safety of these AMPs. |
ArticleNumber | 50 |
Author | Memariani, Hamed Moravvej, Hamideh Goudarzi, Hossein Memariani, Mojtaba Robati, Reza Mahmoud |
Author_xml | – sequence: 1 givenname: Mojtaba orcidid: 0000-0002-4964-3117 surname: Memariani fullname: Memariani, Mojtaba organization: Skin Research Center, Shahid Beheshti University of Medical Sciences – sequence: 2 givenname: Hamed orcidid: 0000-0003-1026-140X surname: Memariani fullname: Memariani, Hamed email: h.memariani@gmail.com organization: Skin Research Center, Shahid Beheshti University of Medical Sciences – sequence: 3 givenname: Hamideh orcidid: 0000-0002-9425-7282 surname: Moravvej fullname: Moravvej, Hamideh email: hamideh_moravvej@yahoo.com, hamidehmoravej@sbmu.ac.ir organization: Skin Research Center, Shahid Beheshti University of Medical Sciences – sequence: 4 givenname: Hossein surname: Goudarzi fullname: Goudarzi, Hossein organization: Department of Microbiology, School of Medicine, Shahid Beheshti University of Medical Sciences – sequence: 5 givenname: Reza Mahmoud orcidid: 0000-0002-7947-8642 surname: Robati fullname: Robati, Reza Mahmoud organization: Skin Research Center, Shahid Beheshti University of Medical Sciences |
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Copyright | The Author(s), under exclusive licence to Springer Nature B.V. 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. |
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Snippet | Antimicrobial peptides (AMPs) have recently been the subject of extensive research in both academia and commercial sectors because of their rapid,... |
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SubjectTerms | Animal Anatomy Antimicrobial peptides Atomic force microscopy Biochemistry Biomedical and Life Sciences Cell walls Circular dichroism Conformation Cytotoxicity Drug resistance Fourier transforms Histology Life Sciences Microbicides Minimum inhibitory concentration Molecular Medicine Morphology Peptides Pharmaceutical Sciences/Technology Pharmacology/Toxicology Polymer Sciences Polysaccharides Yeast |
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Title | Anticandidal Activity and Mechanism of Action of Several Cationic Chimeric Antimicrobial Peptides |
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