Cargando…

Antimicrobial and Anti-Biofilm Peptide Octominin for Controlling Multidrug-Resistant Acinetobacter baumannii

Acinetobacter baumannii is a serious nosocomial pathogen with multiple drug resistance (MDR), the control of which has become challenging due to the currently used antibiotics. Our main objective in this study is to determine the antibacterial and antibiofilm activities of the antimicrobial peptide,...

Descripción completa

Detalles Bibliográficos
Autores principales: Jayathilaka, E. H. T. Thulshan, Rajapaksha, Dinusha C., Nikapitiya, Chamilani, De Zoysa, Mahanama, Whang, Ilson
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8161146/
https://www.ncbi.nlm.nih.gov/pubmed/34069596
http://dx.doi.org/10.3390/ijms22105353
_version_ 1783700441643614208
author Jayathilaka, E. H. T. Thulshan
Rajapaksha, Dinusha C.
Nikapitiya, Chamilani
De Zoysa, Mahanama
Whang, Ilson
author_facet Jayathilaka, E. H. T. Thulshan
Rajapaksha, Dinusha C.
Nikapitiya, Chamilani
De Zoysa, Mahanama
Whang, Ilson
author_sort Jayathilaka, E. H. T. Thulshan
collection PubMed
description Acinetobacter baumannii is a serious nosocomial pathogen with multiple drug resistance (MDR), the control of which has become challenging due to the currently used antibiotics. Our main objective in this study is to determine the antibacterial and antibiofilm activities of the antimicrobial peptide, Octominin, against MDR A. baumannii and derive its possible modes of actions. Octominin showed significant bactericidal effects at a low minimum inhibitory concentration (MIC) and the minimum bactericidal concentration (MBC) of 5 and 10 µg/mL, respectively. Time-kill kinetic analysis and bacterial viability tests revealed that Octominin showed a concentration-dependent antibacterial activity. Field-emission scanning electron microscopy (FE-SEM) analysis revealed that Octominin treatment altered the morphology and membrane structure of A. baumannii. Propidium iodide (PI) and reactive oxygen species (ROS) generation assays showed that Octominin increased the membrane permeability and ROS generation in A. baumannii, thereby causing bacterial cell death. Further, a lipopolysaccharides (LPS) binding assay showed an Octominin concentration-dependent LPS neutralization ability. Biofilm formation inhibition and eradication assays further revealed that Octominin inhibited biofilm formation and showed a high biofilm eradication activity against A. baumannii. Furthermore, up to a concentration of 100 µg/mL, Octominin caused no hemolysis and cell viability changes in mammalian cells. An in vivo study in zebrafish showed that the Octominin-treated group had a significantly higher relative percentage survival (54.1%) than the untreated group (16.6%). Additionally, a reduced bacterial load and fewer alterations in histological analysis confirmed the successful control of A. baumannii by Octominin in vivo. Collectively, these data suggest that Octominin exhibits significant antibacterial and antibiofilm activities against the multidrug-resistant A. baumannii, and this AMP can be developed further as a potent AMP for the control of antibiotic resistance.
format Online
Article
Text
id pubmed-8161146
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-81611462021-05-29 Antimicrobial and Anti-Biofilm Peptide Octominin for Controlling Multidrug-Resistant Acinetobacter baumannii Jayathilaka, E. H. T. Thulshan Rajapaksha, Dinusha C. Nikapitiya, Chamilani De Zoysa, Mahanama Whang, Ilson Int J Mol Sci Article Acinetobacter baumannii is a serious nosocomial pathogen with multiple drug resistance (MDR), the control of which has become challenging due to the currently used antibiotics. Our main objective in this study is to determine the antibacterial and antibiofilm activities of the antimicrobial peptide, Octominin, against MDR A. baumannii and derive its possible modes of actions. Octominin showed significant bactericidal effects at a low minimum inhibitory concentration (MIC) and the minimum bactericidal concentration (MBC) of 5 and 10 µg/mL, respectively. Time-kill kinetic analysis and bacterial viability tests revealed that Octominin showed a concentration-dependent antibacterial activity. Field-emission scanning electron microscopy (FE-SEM) analysis revealed that Octominin treatment altered the morphology and membrane structure of A. baumannii. Propidium iodide (PI) and reactive oxygen species (ROS) generation assays showed that Octominin increased the membrane permeability and ROS generation in A. baumannii, thereby causing bacterial cell death. Further, a lipopolysaccharides (LPS) binding assay showed an Octominin concentration-dependent LPS neutralization ability. Biofilm formation inhibition and eradication assays further revealed that Octominin inhibited biofilm formation and showed a high biofilm eradication activity against A. baumannii. Furthermore, up to a concentration of 100 µg/mL, Octominin caused no hemolysis and cell viability changes in mammalian cells. An in vivo study in zebrafish showed that the Octominin-treated group had a significantly higher relative percentage survival (54.1%) than the untreated group (16.6%). Additionally, a reduced bacterial load and fewer alterations in histological analysis confirmed the successful control of A. baumannii by Octominin in vivo. Collectively, these data suggest that Octominin exhibits significant antibacterial and antibiofilm activities against the multidrug-resistant A. baumannii, and this AMP can be developed further as a potent AMP for the control of antibiotic resistance. MDPI 2021-05-19 /pmc/articles/PMC8161146/ /pubmed/34069596 http://dx.doi.org/10.3390/ijms22105353 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Jayathilaka, E. H. T. Thulshan
Rajapaksha, Dinusha C.
Nikapitiya, Chamilani
De Zoysa, Mahanama
Whang, Ilson
Antimicrobial and Anti-Biofilm Peptide Octominin for Controlling Multidrug-Resistant Acinetobacter baumannii
title Antimicrobial and Anti-Biofilm Peptide Octominin for Controlling Multidrug-Resistant Acinetobacter baumannii
title_full Antimicrobial and Anti-Biofilm Peptide Octominin for Controlling Multidrug-Resistant Acinetobacter baumannii
title_fullStr Antimicrobial and Anti-Biofilm Peptide Octominin for Controlling Multidrug-Resistant Acinetobacter baumannii
title_full_unstemmed Antimicrobial and Anti-Biofilm Peptide Octominin for Controlling Multidrug-Resistant Acinetobacter baumannii
title_short Antimicrobial and Anti-Biofilm Peptide Octominin for Controlling Multidrug-Resistant Acinetobacter baumannii
title_sort antimicrobial and anti-biofilm peptide octominin for controlling multidrug-resistant acinetobacter baumannii
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8161146/
https://www.ncbi.nlm.nih.gov/pubmed/34069596
http://dx.doi.org/10.3390/ijms22105353
work_keys_str_mv AT jayathilakaehtthulshan antimicrobialandantibiofilmpeptideoctomininforcontrollingmultidrugresistantacinetobacterbaumannii
AT rajapakshadinushac antimicrobialandantibiofilmpeptideoctomininforcontrollingmultidrugresistantacinetobacterbaumannii
AT nikapitiyachamilani antimicrobialandantibiofilmpeptideoctomininforcontrollingmultidrugresistantacinetobacterbaumannii
AT dezoysamahanama antimicrobialandantibiofilmpeptideoctomininforcontrollingmultidrugresistantacinetobacterbaumannii
AT whangilson antimicrobialandantibiofilmpeptideoctomininforcontrollingmultidrugresistantacinetobacterbaumannii