2021
DOI: 10.1016/j.ejmech.2021.113433
|View full text |Cite
|
Sign up to set email alerts
|

An optimized analog of antimicrobial peptide Jelleine-1 shows enhanced antimicrobial activity against multidrug resistant P. aeruginosa and negligible toxicity in vitro and in vivo

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

1
34
0

Year Published

2021
2021
2024
2024

Publication Types

Select...
8
1

Relationship

1
8

Authors

Journals

citations
Cited by 35 publications
(39 citation statements)
references
References 52 publications
1
34
0
Order By: Relevance
“…The peptides R23F, R23DI, and R23EI demonstrated MIC around 12 μM against individual strains of MRSA and S. aureus indicating their antimicrobial activity at the level of peptide antibiotic polymyxin B [ 56 ]. The antimicrobial effect of the peptides against other strains and pathogenic microorganisms can be increased due to amino acid modifications of the sequence of antimicrobial peptides, for example as was done for jelleine-1 [ 57 ]. Based on the experiments carried out on the effect of the R23DI peptide on S. aureus and MRSA, it can be concluded that the R23DI peptide disrupts the cell wall of MRSA strain ATCC 43300 cells ( Figure 9 ) and does not destroy the cell wall when exposed to the S. aureus strain 209P cells ( Figure 10 ).…”
Section: Discussionmentioning
confidence: 99%
“…The peptides R23F, R23DI, and R23EI demonstrated MIC around 12 μM against individual strains of MRSA and S. aureus indicating their antimicrobial activity at the level of peptide antibiotic polymyxin B [ 56 ]. The antimicrobial effect of the peptides against other strains and pathogenic microorganisms can be increased due to amino acid modifications of the sequence of antimicrobial peptides, for example as was done for jelleine-1 [ 57 ]. Based on the experiments carried out on the effect of the R23DI peptide on S. aureus and MRSA, it can be concluded that the R23DI peptide disrupts the cell wall of MRSA strain ATCC 43300 cells ( Figure 9 ) and does not destroy the cell wall when exposed to the S. aureus strain 209P cells ( Figure 10 ).…”
Section: Discussionmentioning
confidence: 99%
“…Also, synergistic effect and anti-biofilm activity of an AMP (Pt5–1c; a derivative of phosvitin) along with oxacillin, vancomycin, streptomycin and azithromycin has been suggested against MDR pathogens such as S. aureus , E. coli and K. pneumoniae [216] . An analog of AMP Jelleine-1 (extracted from the royal jelly of honeybees) has been implicated in the potent inhibition of biofilm formation of MDR pathogen P. aeruginosa [217] . Oh et al has shown the anti-biofilm and anti-inflammatory effects of Lycosin-II (an AMP isolated from spiders) against MDR S. aureus and P. aeruginosa infections [218] .…”
Section: Application Of Amps Against Mdr Pathogensmentioning
confidence: 99%
“…The authors demonstrated that jelleine-I has an inhibitory effect against this certain pathogen, and the development of antimicrobial agents that involve jelleine-I is feasible [100]. Moreover, Zhou et al (2021) [101] developed several jelleine-I analogs that exhibit intensified antimicrobial effects against P. aeruginosa. By investigating the activity of the developed analogs, the authors concluded that one certain analog, that expresses in its sequence additional arginine and leucine, displays improved antibacterial effect against P. aeruginosa.…”
Section: Rj Against P Aeruginosamentioning
confidence: 99%